ID

24040

Beschrijving

Responsible Party: Dr.Rahul Navinchandra Bakhda MS., Consultant Ophthalmologist, Ex-Resident, M and J Western Regional Institute of Ophthalmology, B. J. Medical College, Ahmedabad ClinicalTrials.gov Identifier: NCT03076619 History of Changes Other Study ID Numbers: Postgraduation Thesis DRKS00011324 ( Registry Identifier: The German Clinical Trials Register -Deutsche Register Klinischer Studien ) ChiCTR-OOC-16010171 ( Registry Identifier: Chinese Clinical Trial Registry-ChiCTR ) UMIN000024722 ( Registry Identifier: UMIN Clinical Trials Registry (UMIN-CTR) ) U1111-1189-6165 ( Registry Identifier: International Clinical Trials Registry Platform (ICTRP) ) TCTR20161221005 ( Registry Identifier: Thai Clinical Trials Registry (TCTR) ) Study First Received: October 30, 2016 Last Updated: March 10, 2017 A Clinical Study of Fundus Findings in Toxaemia of Pregnancy ODM derived from: https://clinicaltrials.gov/ct2/show/NCT03076619

Link

https://clinicaltrials.gov/ct2/show/NCT03076619

Trefwoorden

  1. 23-07-17 23-07-17 -
Geüploaded op

23 juli 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Pregnancy NCT03076619 DRKS00011324

Eligibility Pregnancy NCT03076619 DRKS00011324

Default Itemgroup
Beschrijving

Default Itemgroup

Ages Eligible for Study: 18 Years to 42 Years (Adult)
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
Female
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
Cases of Pregnancy Induced Hypertension.
Beschrijving

Pregnancy Induced Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C1411577
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Cases complicated by malignancy, renal, liver or other secondary manifestations.
Beschrijving

Malignancy, Secondary Hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
UMLS CUI [2]
C0155616
Healthy Volunteers
Beschrijving

Control Group

Datatype

boolean

Alias
UMLS CUI [1]
C0009932

Similar models

Eligibility Pregnancy NCT03076619 DRKS00011324

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
Ages Eligible for Study: 18 Years to 42 Years (Adult)
boolean
C0001779 (UMLS CUI [1])
Gender
Item
Female
boolean
C0079399 (UMLS CUI [1])
Pregnancy Induced Hypertension
Item
Cases of Pregnancy Induced Hypertension.
boolean
C1411577 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Malignancy, Secondary Hypertension
Item
Cases complicated by malignancy, renal, liver or other secondary manifestations.
boolean
C0006826 (UMLS CUI [1])
C0155616 (UMLS CUI [2])
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])

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