ID
16867
Beschreibung
Study Sponsor: Astellas Study Title Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study Medicine or Vaccine (generic name) capsaicin Sponsor Identification Number QTZ-EC-0002 Trial Registry Identification Number(#'s) NCT01416116 EudraCT Number: 2010-023258-34 Medical Condition Neuropathic pain Phase Phase 4 http://clinicaltrials.gov/show/NCT01416116 Treatment Visit Form 2/5: Randomization Vital Signs: 75 mins prior to patch application Vital Signs: 15 mins prior to patch application Post patch application and post patch removal
Link
http://clinicaltrials.gov/show/NCT01416116
Stichworte
Versionen (2)
- 24.07.16 24.07.16 -
- 11.08.16 11.08.16 -
Hochgeladen am
11. August 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Treatment Visit Form 2/5 Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116
Treatment Visit Form 2/5 Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116
Beschreibung
Vital Signs: 75 mins prior to patch application
Beschreibung
Assessment Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2985720
Beschreibung
Scheduled Time
Datentyp
time
Alias
- UMLS CUI [1]
- C0086960
Beschreibung
Assessment Time
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Beschreibung
Position
Datentyp
integer
Alias
- UMLS CUI [1]
- C0733755
Beschreibung
For any AE, please provide details on the 'Adverse Event' form.
Datentyp
text
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschreibung
Diastolic Blood Pressure
Datentyp
text
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschreibung
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0232117
Beschreibung
Vital Signs: 15 mins prior to patch application
Beschreibung
Assessment Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2985720
Beschreibung
Scheduled Time
Datentyp
time
Alias
- UMLS CUI [1]
- C0086960
Beschreibung
Assessment Time
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Beschreibung
Position
Datentyp
integer
Alias
- UMLS CUI [1]
- C0733755
Beschreibung
For any AE, please provide details on the 'Adverse Event' form.
Datentyp
text
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschreibung
Diastolic Blood Pressure
Datentyp
text
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschreibung
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0232117
Beschreibung
Vital Signs: Post patch application and post patch rGeemnoevraatl
Beschreibung
Assessment Date
Datentyp
date
Alias
- UMLS CUI [1]
- C2985720
Beschreibung
Scheduled Time
Datentyp
time
Alias
- UMLS CUI [1]
- C0086960
Beschreibung
Assessment Time
Datentyp
time
Alias
- UMLS CUI [1,1]
- C0518766
- UMLS CUI [1,2]
- C0040223
Beschreibung
Position
Datentyp
integer
Alias
- UMLS CUI [1]
- C0733755
Beschreibung
For any AE, please provide details on the 'Adverse Event' form.
Datentyp
text
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0871470
Beschreibung
Diastolic Blood Pressure
Datentyp
text
Maßeinheiten
- mmHg
Alias
- UMLS CUI [1]
- C0428883
Beschreibung
Record any clinically significant abnormal findings/conditions identified during the exam on the Current Medical and Surgical History and/or Adverse Event form.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0232117
Ähnliche Modelle
Treatment Visit Form 2/5 Tolerability of QUTENZA™ When Applied After Pre-treatment With Lidocaine or Tramadol in Subjects With Peripheral Neuropathic Pain - A Randomized, Multi-center, Assessor-blinded Study NCT01416116
C0011008 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,2])
C0034656 (UMLS CUI [1,3])
C0034656 (UMLS CUI [1,2])
C0441833 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])