ID

24265

Description

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

Keywords

  1. 7/28/17 7/28/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 28, 2017

DOI

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License

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 Randomisation Visit URINALYSIS LOCAL NCT00079911

GSK Study Randomisation Visit URINALYSIS LOCAL NCT00079911

Study administration
Description

Study administration

Subject Identifier
Description

Subject Identifier

Data type

integer

Alias
UMLS CUI [1]
C2348585
Visit Date
Description

Visit Date

Data type

date

Measurement units
  • DD/MMM/YY
Alias
UMLS CUI [1]
C1320303
DD/MMM/YY
URINALYSIS - LOCAL
Description

URINALYSIS - LOCAL

Date sample taken
Description

Date sample taken

Data type

date

Measurement units
  • DD/MMM/YY
Alias
UMLS CUI [1,1]
C1302413
UMLS CUI [1,2]
C0042036
DD/MMM/YY
Result of dipstick
Description

If positive, record results of individual tests below.

Data type

text

Alias
UMLS CUI [1,1]
C1160927
UMLS CUI [1,2]
C0456984
Blood
Description

Blood urine test

Data type

text

Alias
UMLS CUI [1]
C0202514
Protein
Description

Protein urine test

Data type

text

Alias
UMLS CUI [1]
C0262923

Similar models

GSK Study Randomisation Visit URINALYSIS LOCAL NCT00079911

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Study administration
Subject Identifier
Item
Subject Identifier
integer
C2348585 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Item Group
URINALYSIS - LOCAL
Date sample taken
Item
Date sample taken
date
C1302413 (UMLS CUI [1,1])
C0042036 (UMLS CUI [1,2])
Item
Result of dipstick
text
C1160927 (UMLS CUI [1,1])
C0456984 (UMLS CUI [1,2])
Code List
Result of dipstick
CL Item
Negative (NEG)
CL Item
Positive (POS)
CL Item
No result (NR)
Item
Blood
text
C0202514 (UMLS CUI [1])
Code List
Blood
CL Item
none or negative (NEG)
CL Item
trace (TRA)
CL Item
+ or 1+ (1+)
CL Item
++ or 2+ (2+)
CL Item
+++ or 3+ (3+)
CL Item
++++ or 4+ (4+)
CL Item
+++++ or 5+ (5+)
Item
Protein
text
C0262923 (UMLS CUI [1])
Code List
Protein
CL Item
none or negative (NEG)
CL Item
trace (TRA)
CL Item
+ or 1+ (1+)
CL Item
++ or 2+ (2+)
CL Item
+++ or 3+ (3+)
CL Item
++++ or 4+ (4+)
CL Item
+++++ or 5+ (5+)

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