ID

24390

Beschrijving

NCT00079911 Study ID 100181 Clinical Study ID HS2100181 Study Title: An International, Randomized, Double-Blind, Placebo-Controlled Study of Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons with CD4+ lymphocyte count <100 cells/mm3. Patient Level Data Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00079911 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Terminated Generic Name: valaciclovir Trade Name: ZELITREX,Valtrex,RAPIVIR,Novirus Study Indication: Genital Herpes; HIV infection

Trefwoorden

Versies (1)
  1. 30-07-17 30-07-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

30 juli 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons CONCOMITANT MEDICATIONS NCT00079911

Engels

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons CONCOMITANT MEDICATIONS NCT00079911

1 Formulieren  
Study administration
Beschrijving

Study administration

Subject Identifier
Beschrijving

Subject Identifier

Datatype

integer

Alias
UMLS CUI [1]
C2348585
CONCOMITANT MEDICATIONS
Beschrijving

CONCOMITANT MEDICATIONS

Were any concomitant medications taken by the subject during the study?
Beschrijving

If Yes, record each medication on a separate line using Trade Names where possible.

Datatype

text

Alias
UMLS CUI [1]
C2347852
CONCOMITANT MEDICATIONS
Beschrijving

CONCOMITANT MEDICATIONS

Drug Name
Beschrijving

(Trade Name preferred)

Datatype

text

Alias
UMLS CUI [1]
C0013227
Start Date
Beschrijving

drug start date

Datatype

date

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0808070
Taken Prior to Study?
Beschrijving

Taken Prior to Study

Datatype

text

Alias
UMLS CUI [1]
C2826667
Stop Date
Beschrijving

stop date

Datatype

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
Ongoing Medication?
Beschrijving

Ongoing Medication

Datatype

text

Alias
UMLS CUI [1]
C2826666
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Similar models

GSK Valaciclovir for the Suppression and Episodic Treatment of Genital HSV Infection in HIV-Infected Persons CONCOMITANT MEDICATIONS NCT00079911

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Study administration
Subject Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Item Group
CONCOMITANT MEDICATIONS
Item
Were any concomitant medications taken by the subject during the study?
text
C2347852 (UMLS CUI [1])
concomitant medications
Code List
Were any concomitant medications taken by the subject during the study?
CL Item
Yes (Y)
CL Item
No (N)
Item Group
CONCOMITANT MEDICATIONS
Drug Name
Item
Drug Name
text
C0013227 (UMLS CUI [1])
drug start date
Item
Start Date
date
C0013216 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Item
Taken Prior to Study?
text
C2826667 (UMLS CUI [1])
concomitant medications
Code List
Taken Prior to Study?
CL Item
Yes (Y)
CL Item
No (N)
stop date
Item
Stop Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Item
Ongoing Medication?
text
C2826666 (UMLS CUI [1])
concomitant medications
Code List
Ongoing Medication?
CL Item
Yes (Y)
CL Item
No (N)
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