ID

39025

Beschrijving

Intravitreal Ranibizumab Combined With Panretinal Photocoagulation in Patients With Proliferative Diabetic Retinopathy; ODM derived from: https://clinicaltrials.gov/show/NCT01746563

Link

https://clinicaltrials.gov/show/NCT01746563

Trefwoorden

  1. 21-11-19 21-11-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

21 november 2019

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Diabetic Retinopathy NCT01746563

Eligibility Diabetic Retinopathy NCT01746563

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
naive proliferative diabetic retinopathy eyes.
Beschrijving

Proliferative diabetic retinopathy | Therapy naive Eyes

Datatype

boolean

Alias
UMLS CUI [1]
C0154830
UMLS CUI [2,1]
C0919936
UMLS CUI [2,2]
C0015392
best corrected-visual acuity at baseline > 20/320 in the study eye
Beschrijving

Best corrected visual acuity Clinical Trial Eye

Datatype

boolean

Alias
UMLS CUI [1,1]
C1690532
UMLS CUI [1,2]
C0008976
UMLS CUI [1,3]
C0015392
patients with and without diabetic macular edema
Beschrijving

Diabetic macular edema | Diabetic macular edema Absent

Datatype

boolean

Alias
UMLS CUI [1]
C0730285
UMLS CUI [2,1]
C0730285
UMLS CUI [2,2]
C0332197
type ii diabetic subjects as defined by the world health organization aged ≥ 18 years.
Beschrijving

Non-Insulin-Dependent Diabetes Mellitus WHO classification | Age

Datatype

boolean

Alias
UMLS CUI [1,1]
C0011860
UMLS CUI [1,2]
C4267671
UMLS CUI [2]
C0001779
women must be using effective contraception
Beschrijving

Gender Contraceptive methods

Datatype

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0700589
ability to provide written informed consent.
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
indication of panretinal photocoagulation in both eyes
Beschrijving

Indication Panretinal photocoagulation Both eyes

Datatype

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0730064
UMLS CUI [1,3]
C0229118
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
vitreous hemorrhage or pre-retinal hemorrhage
Beschrijving

Vitreous Hemorrhage | Preretinal hemorrhage

Datatype

boolean

Alias
UMLS CUI [1]
C0042909
UMLS CUI [2]
C4316879
eyes with prior scatter (panretinal) or focal/grid photocoagulation, within the previous 6 months
Beschrijving

Eyes Panretinal photocoagulation Previous | Eyes Focal photocoagulation | Eyes Grid photocoagulation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0015392
UMLS CUI [1,2]
C0730064
UMLS CUI [1,3]
C0205156
UMLS CUI [2,1]
C0015392
UMLS CUI [2,2]
C1302105
UMLS CUI [3,1]
C0015392
UMLS CUI [3,2]
C1302035
atrophy/scarring/fibrosis/ hard exudates involving the center of the macula.
Beschrijving

Atrophy Involving Center of macula | Scarring Involving Center of macula | Fibrosis Involving Center of macula | Hard exudates Involving Center of macula

Datatype

boolean

Alias
UMLS CUI [1,1]
C0333641
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C0016622
UMLS CUI [2,1]
C0008767
UMLS CUI [2,2]
C1314939
UMLS CUI [2,3]
C0016622
UMLS CUI [3,1]
C0016059
UMLS CUI [3,2]
C1314939
UMLS CUI [3,3]
C0016622
UMLS CUI [4,1]
C0423410
UMLS CUI [4,2]
C1314939
UMLS CUI [4,3]
C0016622
cataract
Beschrijving

Cataract

Datatype

boolean

Alias
UMLS CUI [1]
C0086543
any intraocular surgery within 6 months before trial enrollment
Beschrijving

Operative Surgical Procedure Intraocular

Datatype

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C3282905
previous vitrectomy.
Beschrijving

Vitrectomy

Datatype

boolean

Alias
UMLS CUI [1]
C0042903
any of the following underlying systemic diseases:
Beschrijving

Systemic disease Specified

Datatype

boolean

Alias
UMLS CUI [1,1]
C0442893
UMLS CUI [1,2]
C0205369
history or evidence of severe cardiac disease or previous thrombus-embolic event
Beschrijving

Heart Disease Severe | Thromboembolism

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0040038

Similar models

Eligibility Diabetic Retinopathy NCT01746563

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Proliferative diabetic retinopathy | Therapy naive Eyes
Item
naive proliferative diabetic retinopathy eyes.
boolean
C0154830 (UMLS CUI [1])
C0919936 (UMLS CUI [2,1])
C0015392 (UMLS CUI [2,2])
Best corrected visual acuity Clinical Trial Eye
Item
best corrected-visual acuity at baseline > 20/320 in the study eye
boolean
C1690532 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0015392 (UMLS CUI [1,3])
Diabetic macular edema | Diabetic macular edema Absent
Item
patients with and without diabetic macular edema
boolean
C0730285 (UMLS CUI [1])
C0730285 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Non-Insulin-Dependent Diabetes Mellitus WHO classification | Age
Item
type ii diabetic subjects as defined by the world health organization aged ≥ 18 years.
boolean
C0011860 (UMLS CUI [1,1])
C4267671 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Gender Contraceptive methods
Item
women must be using effective contraception
boolean
C0079399 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
ability to provide written informed consent.
boolean
C0021430 (UMLS CUI [1])
Indication Panretinal photocoagulation Both eyes
Item
indication of panretinal photocoagulation in both eyes
boolean
C3146298 (UMLS CUI [1,1])
C0730064 (UMLS CUI [1,2])
C0229118 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Vitreous Hemorrhage | Preretinal hemorrhage
Item
vitreous hemorrhage or pre-retinal hemorrhage
boolean
C0042909 (UMLS CUI [1])
C4316879 (UMLS CUI [2])
Eyes Panretinal photocoagulation Previous | Eyes Focal photocoagulation | Eyes Grid photocoagulation
Item
eyes with prior scatter (panretinal) or focal/grid photocoagulation, within the previous 6 months
boolean
C0015392 (UMLS CUI [1,1])
C0730064 (UMLS CUI [1,2])
C0205156 (UMLS CUI [1,3])
C0015392 (UMLS CUI [2,1])
C1302105 (UMLS CUI [2,2])
C0015392 (UMLS CUI [3,1])
C1302035 (UMLS CUI [3,2])
Atrophy Involving Center of macula | Scarring Involving Center of macula | Fibrosis Involving Center of macula | Hard exudates Involving Center of macula
Item
atrophy/scarring/fibrosis/ hard exudates involving the center of the macula.
boolean
C0333641 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C0016622 (UMLS CUI [1,3])
C0008767 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0016622 (UMLS CUI [2,3])
C0016059 (UMLS CUI [3,1])
C1314939 (UMLS CUI [3,2])
C0016622 (UMLS CUI [3,3])
C0423410 (UMLS CUI [4,1])
C1314939 (UMLS CUI [4,2])
C0016622 (UMLS CUI [4,3])
Cataract
Item
cataract
boolean
C0086543 (UMLS CUI [1])
Operative Surgical Procedure Intraocular
Item
any intraocular surgery within 6 months before trial enrollment
boolean
C0543467 (UMLS CUI [1,1])
C3282905 (UMLS CUI [1,2])
Vitrectomy
Item
previous vitrectomy.
boolean
C0042903 (UMLS CUI [1])
Systemic disease Specified
Item
any of the following underlying systemic diseases:
boolean
C0442893 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
Heart Disease Severe | Thromboembolism
Item
history or evidence of severe cardiac disease or previous thrombus-embolic event
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0040038 (UMLS CUI [2])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial