ID
38670
Beskrivning
Study ID: 101468/205 Clinical Study ID: 101468/205 Study Title:A 12-Week, Double-Blind, Placebo Controlled, Parallel Group Study to Assess the Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00197080 Sponsor: GlaxoSmithKline Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication: Restless Legs Syndrome
Nyckelord
Versioner (2)
- 2019-02-18 2019-02-18 -
- 2019-10-30 2019-10-30 - Sarah Riepenhausen
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
30 oktober 2019
DOI
För en begäran logga in.
Licens
Creative Commons BY-NC 3.0
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Efficacy and Safety of Ropinirole XR (Extended Release) in Patients with Restless Legs Syndrome NCT00197080
Investigational Product; Status of Treatment Blind; Pharmacogenetic Research; Concomitant Medication; Non-Serious Adverse Events; Serious Adverse Events
Beskrivning
Investigational Product
Alias
- UMLS CUI-1
- C0304229
Beskrivning
e.g., 1
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0304229
Beskrivning
Investigational Product Start Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beskrivning
Investigational Product Stop Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Beskrivning
Has the subject missed investigational product for >2 consecutive days?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0457454
- UMLS CUI [1,3]
- C0439228
- UMLS CUI [1,4]
- C1707491
Beskrivning
Investigational Product Container Number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0600091
Beskrivning
Investigational Product Container Number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0600091
Beskrivning
Status of Treatment Blind
Alias
- UMLS CUI-1
- C0749659
- UMLS CUI-2
- C2347038
Beskrivning
If Yes, complete the following
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0749659
- UMLS CUI [1,2]
- C2347038
Beskrivning
Date blind broken
Datatyp
date
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0011008
Beskrivning
Complete Non-Serious Adverse Events or Serious Adverse Event pages, as appropriate.
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
Beskrivning
If other reason for blind broken, specify.
Datatyp
text
Alias
- UMLS CUI [1,1]
- C3897431
- UMLS CUI [1,2]
- C0392360
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beskrivning
Consent for Pharmacogenetic Research
Alias
- UMLS CUI-1
- C0021430
- UMLS CUI-2
- C2347500
Beskrivning
If Yes, record the date informed consent obtained for PGx-Pharmacogenetic research If No, check one reason
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
Beskrivning
Date informed consent obtained for PGx-Pharmacogenetic research
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C0011008
Beskrivning
Reason for informed consent for PGx-Pharmacogenetic research not obtained
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1882120
- UMLS CUI [1,4]
- C0392360
Beskrivning
Other reason for informed consent for PGx-Pharmacogenetic research not obtained
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C2347500
- UMLS CUI [1,3]
- C1882120
- UMLS CUI [1,4]
- C0392360
- UMLS CUI [1,5]
- C0205394
- UMLS CUI [1,6]
- C2348235
Beskrivning
PGx - Blood Sample Collection (DNA)
Alias
- UMLS CUI-1
- C0031325
- UMLS CUI-2
- C0005834
- UMLS CUI-3
- C0012854
Beskrivning
PGx - Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Beskrivning
PGx - Blood Sample Destruction
Alias
- UMLS CUI-1
- C0031325
- UMLS CUI-2
- C0370003
- UMLS CUI-3
- C1948029
Beskrivning
If Yes, check one reason
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0031325
- UMLS CUI [1,2]
- C0370003
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Beskrivning
Reason for sample destruction
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C0392360
Beskrivning
If other Reason for sample destruction, specify
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1948029
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C0392360
- UMLS CUI [1,4]
- C0205394
- UMLS CUI [1,5]
- C2348235
Beskrivning
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Beskrivning
If Yes, record each medication on a separate line using Trade Names where possible. If the medication is related to a Non-Serious Adverse Event or Serious Adverse Event, details should be expressed using the same terminology.
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2347852
Beskrivning
Concomitant Medications
Alias
- UMLS CUI-1
- C2347852
Beskrivning
(Trade Name preferred) e.g., Aspirin
Datatyp
text
Alias
- UMLS CUI [1]
- C2360065
Beskrivning
Total Daily Dose
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C2348070
- UMLS CUI [1,2]
- C0439810
Beskrivning
Units
Datatyp
text
Alias
- UMLS CUI [1]
- C1519795
Beskrivning
Reason for Medication
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0392360
- UMLS CUI [1,2]
- C0013227
Beskrivning
Start Date
Datatyp
date
Alias
- UMLS CUI [1]
- C2826734
Beskrivning
Medication Taken Prior to Study?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826667
Beskrivning
Concomitant Medication Stop Date
Datatyp
date
Alias
- UMLS CUI [1]
- C2826744
Beskrivning
Ongoing Medication?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Beskrivning
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Beskrivning
Non-Serious Adverse Events
Alias
- UMLS CUI-1
- C1518404
Beskrivning
Diagnosis Only (if known), Otherwise Sign/Symptom
Datatyp
text
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
Non-Serious Adverse Event Start Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2697888
Beskrivning
Non-Serious Adverse Event Start Time
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1301880
Beskrivning
Non-Serious Adverse Event Outcome
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Beskrivning
Non-Serious Adverse Event End Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Beskrivning
Non-Serious Adverse Event End Time
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1522314
Beskrivning
Non-Serious Adverse Event Frequency
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Beskrivning
Non-Serious Adverse Event Maximum Intensity
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Beskrivning
Action Taken with Investigational Product(s) as a Result of the Non-Serious AE
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1518404
Beskrivning
Withdrawal
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1710677
- UMLS CUI [1,2]
- C1518404
Beskrivning
Relationship to Investigational Product(s)
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0439849
Beskrivning
Time to Onset Since Last Dose
Datatyp
time
Måttenheter
- Hr(s):Min(s)
Alias
- UMLS CUI [1,1]
- C0449244
- UMLS CUI [1,2]
- C1762893
Beskrivning
Serious Adverse Events
Alias
- UMLS CUI-1
- C1519255
Beskrivning
If Yes, record details below.
Datatyp
boolean
Alias
- UMLS CUI [1]
- C1519255
Beskrivning
Subject Identifier
Datatyp
integer
Alias
- UMLS CUI [1]
- C2348585
Beskrivning
Centre Number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0600091
- UMLS CUI [1,2]
- C0019994
Beskrivning
Randomisation Number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0034656
- UMLS CUI [1,2]
- C0237753
Beskrivning
Serious Adverse Events - Section 1
Alias
- UMLS CUI-1
- C1519255
Beskrivning
Diagnosis Only (if known) Otherwise Sign/Symptom
Datatyp
text
Alias
- UMLS CUI [1]
- C0877248
Beskrivning
Serious Adverse Event Start Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0808070
Beskrivning
Serious Adverse Event Start Time
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1301880
Beskrivning
Serious Adverse Event Outcome
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1705586
Beskrivning
If fatal, record date of death.
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0806020
Beskrivning
Serious Adverse Event End Time
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1522314
Beskrivning
Serious Adverse Event Maximum Intensity
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0806909
Beskrivning
Action Taken with Investigational Product(s) as a Result of the SAE
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1704758
- UMLS CUI [1,2]
- C1519255
Beskrivning
If yes, Complete Study Conclusion page and check Adverse event as reason for withdrawal.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C2349954
- UMLS CUI [1,2]
- C1519255
Beskrivning
Relationship to Investigational Product(s)
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0085978
- UMLS CUI [1,3]
- C1519255
Beskrivning
Time to Onset Since Last Dose
Datatyp
time
Måttenheter
- Hr(s):Min(s)
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0946444
- UMLS CUI [1,3]
- C0449244
Beskrivning
If Yes, summarise findings in Section 11 Narrative Remarks of this SAE form.
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0004398
- UMLS CUI [1,2]
- C1519255
Beskrivning
Serious Adverse Events - Section 2 (Seriousness)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C1710056
Beskrivning
Seriousness
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710056
Beskrivning
If other Reason for considering this a SAE, please specify.
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C1710056
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beskrivning
Serious Adverse Events - Section 3 (Demography Data)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0011298
Beskrivning
Serious Adverse Events - Section 4
Alias
- UMLS CUI-1
- C1519255
Beskrivning
If Investigational Product(s) was Stopped, Did the Reported Event(s) Recur After Further Investigational Product(s) were Administered?
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0457454
- UMLS CUI [2,1]
- C1519255
- UMLS CUI [2,2]
- C0034897
Beskrivning
Serious Adverse Events - Section 5 (Possible Cause of SAE)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0085978
Beskrivning
Check all that apply:
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C0085978
- UMLS CUI [2,1]
- C0304229
- UMLS CUI [2,2]
- C0205394
Beskrivning
If other cause, specify
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0085978
- UMLS CUI [1,2]
- C1519255
- UMLS CUI [1,3]
- C0205394
- UMLS CUI [1,4]
- C2348235
Beskrivning
Serious Adverse Events - Medical Conditions
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0012634
Beskrivning
Specify any RELEVANT past or current medical disorders, allergies, surgeries, etc. that can help explain the SAE
Datatyp
text
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0521116
- UMLS CUI [1,3]
- C2347946
- UMLS CUI [2]
- C0020517
- UMLS CUI [3]
- C0543467
Beskrivning
Medical Condition Date of Onset
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0574845
Beskrivning
Condition Present at Time of the SAE?
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C1519255
Beskrivning
If No, Date of Last Occurrence
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C2745955
Beskrivning
Serious Adverse Events - Section 7 (Other relevant Risk Factors)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0035648
- UMLS CUI-3
- C2347946
Beskrivning
Serious Adverse Events - Section 8 (Relevant Concomitant Medication)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2347852
Beskrivning
Trade Name preferred
Datatyp
text
Alias
- UMLS CUI [1]
- C0013227
Beskrivning
Medication Dose
Datatyp
integer
Alias
- UMLS CUI [1]
- C3174092
Beskrivning
Medication Unit
Datatyp
text
Alias
- UMLS CUI [1]
- C2826646
Beskrivning
Medication Frequency
Datatyp
text
Alias
- UMLS CUI [1]
- C3476109
Beskrivning
Medication Route
Datatyp
text
Alias
- UMLS CUI [1]
- C0013153
Beskrivning
Taken Prior to Study?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826667
Beskrivning
Medication Start Date
Datatyp
date
Alias
- UMLS CUI [1]
- C2826734
Beskrivning
Medication Stop Date
Datatyp
date
Alias
- UMLS CUI [1]
- C2826744
Beskrivning
Ongoing Medication?
Datatyp
boolean
Alias
- UMLS CUI [1]
- C2826666
Beskrivning
Reason for Medication
Datatyp
text
Alias
- UMLS CUI [1]
- C2826696
Beskrivning
Serious Adverse Events - Section 9 (Details of Investigational Product(s))
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0304229
Beskrivning
Investigational Product Start Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Beskrivning
Investigational Product Start Time
Datatyp
time
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C1301880
Beskrivning
Start Date of Most Recent Titration to SAE
Datatyp
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0162621
- UMLS CUI [1,3]
- C1519255
- UMLS CUI [1,4]
- C1513491
Beskrivning
Start Time of Most Recent Titration to SAE
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1301880
- UMLS CUI [1,2]
- C0162621
- UMLS CUI [1,3]
- C1519255
- UMLS CUI [1,4]
- C1513491
Beskrivning
Dose of Most Recent Titration
Datatyp
text
Alias
- UMLS CUI [1,1]
- C3174092
- UMLS CUI [1,2]
- C0162621
- UMLS CUI [1,3]
- C1513491
Beskrivning
Was treatment blind broken at investigational site?
Datatyp
integer
Alias
- UMLS CUI [1]
- C3897431
Beskrivning
Serious Adverse Events - Section 10 ( Details of relevant Assessments)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0220825
- UMLS CUI-3
- C2347946
Beskrivning
Serious Adverse Events - Section 11 (Narrative Remarks)
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0947611
Beskrivning
Serious Adverse Events - Investigator's signature
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C2346576
Similar models
Investigational Product; Status of Treatment Blind; Pharmacogenetic Research; Concomitant Medication; Non-Serious Adverse Events; Serious Adverse Events
C0304229 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0457454 (UMLS CUI [1,2])
C0439228 (UMLS CUI [1,3])
C1707491 (UMLS CUI [1,4])
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0180098 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C2347038 (UMLS CUI-2)
C2347038 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C2347500 (UMLS CUI-2)
C2347500 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C2347500 (UMLS CUI [1,2])
C1882120 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,4])
C2347500 (UMLS CUI [1,2])
C1882120 (UMLS CUI [1,3])
C0392360 (UMLS CUI [1,4])
C0205394 (UMLS CUI [1,5])
C2348235 (UMLS CUI [1,6])
C0005834 (UMLS CUI-2)
C0012854 (UMLS CUI-3)
C0005834 (UMLS CUI [1,2])
C0021430 (UMLS CUI-2)
C2349954 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0370003 (UMLS CUI-2)
C1948029 (UMLS CUI-3)
C0370003 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C2348235 (UMLS CUI [1,5])
C0439810 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,2])
C2697888 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C1518404 (UMLS CUI [1,2])
C1518404 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
C1762893 (UMLS CUI [1,2])
C0019994 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C1522314 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0085978 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C0946444 (UMLS CUI [1,2])
C0449244 (UMLS CUI [1,3])
C1519255 (UMLS CUI [1,2])
C1710056 (UMLS CUI-2)
C1710056 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0011298 (UMLS CUI-2)
C0457454 (UMLS CUI [1,2])
C1519255 (UMLS CUI [2,1])
C0034897 (UMLS CUI [2,2])
C0085978 (UMLS CUI-2)
C0085978 (UMLS CUI [1,2])
C0304229 (UMLS CUI [2,1])
C0205394 (UMLS CUI [2,2])
C1519255 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
C2348235 (UMLS CUI [1,4])
C0012634 (UMLS CUI-2)
C0521116 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2])
C0543467 (UMLS CUI [3])
C0574845 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,3])
C0035648 (UMLS CUI-2)
C2347946 (UMLS CUI-3)
C0035648 (UMLS CUI [1,2])
C2347946 (UMLS CUI [1,3])
C2347852 (UMLS CUI-2)
C0304229 (UMLS CUI-2)
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])
C0162621 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C1513491 (UMLS CUI [1,4])
C0162621 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C1513491 (UMLS CUI [1,4])
C0162621 (UMLS CUI [1,2])
C1513491 (UMLS CUI [1,3])
C0220825 (UMLS CUI-2)
C2347946 (UMLS CUI-3)
C2347946 (UMLS CUI [1,2])
C0947611 (UMLS CUI-2)
C2346576 (UMLS CUI-2)