0 Évaluations

ID

32555

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

Mots-clés

  1. 06/11/2018 06/11/2018 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

6 novembre 2018

DOI

Pour une demande vous connecter.

Licence

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

    1. StudyEvent: ODM
      1. Condom Use
    Condom Use
    Description

    Condom Use

    Alias
    UMLS CUI-1
    C3873750
    UMLS CUI-2
    C1524063
    Do you intend to use condoms for every intercourse attempt throughout the study?
    Description

    Latex Condom, Use of, Intention

    Type de données

    boolean

    Alias
    UMLS CUI [1,1]
    C3873750
    UMLS CUI [1,2]
    C1524063
    UMLS CUI [1,3]
    C0162425

    Similar models

    Condom Use

    1. StudyEvent: ODM
      1. Condom Use
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Condom Use
    C3873750 (UMLS CUI-1)
    C1524063 (UMLS CUI-2)
    Latex Condom, Use of, Intention
    Item
    Do you intend to use condoms for every intercourse attempt throughout the study?
    boolean
    C3873750 (UMLS CUI [1,1])
    C1524063 (UMLS CUI [1,2])
    C0162425 (UMLS CUI [1,3])

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