ID

32664

Description

Study ID: 109059 Clinical Study ID: OTB109059 Study Title: TXA107979:A Phase II Study to Evaluate: Delay in Intravaginal Ejaculatory Latency Time (IELT), Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Two Oral Doses of GSK557296 in a Randomized, Double Blind, Placebo-Controlled, Parallel Group Study in Men with Premature Ejaculation Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01021553 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: epelsiban Trade Name: Study Indication: Premature Ejaculation

Keywords

Versions (1)
  1. 11/11/18 11/11/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

November 11, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Delay in IELT, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK557296 in Men with Premature Ejaculation, 109059

English

Randomisation

1 forms  
  1. StudyEvent: ODM
    1. Randomisation
Randomisation
Description

Randomisation

Alias
UMLS CUI-1
C0034656
Was the subject able to be randomised?
Description

Randomization

Data type

boolean

Alias
UMLS CUI [1]
C0034656
Randomisation number
Description

Randomization, numbers

Data type

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Date of randomisation
Description

Randomization, Date in time

Data type

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0011008
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Similar models

Randomisation

1 forms
  1. StudyEvent: ODM
    1. Randomisation
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Randomisation
C0034656 (UMLS CUI-1)
Randomization
Item
Was the subject able to be randomised?
boolean
C0034656 (UMLS CUI [1])
Randomization, numbers
Item
Randomisation number
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Randomization, Date in time
Item
Date of randomisation
integer
C0034656 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
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