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ID

32531

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

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Versions (1)
  1. 06.11.18 06.11.18 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

6. November 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

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    Pregnancy Information

    1 Formulaires  
    1. StudyEvent: ODM
      1. Pregnancy Information
    Pregnancy Information
    Description

    Pregnancy Information

    Alias
    UMLS CUI-1
    C0032961 (Pregnancy)
    SNOMED
    289908002
    LOINC
    LP75920-6
    UMLS CUI-2
    C1533716 (Information)
    Did a female partner of the male subject become pregnant during the study?
    Description

    Pregnancy of Partner, During, Clinical research

    Type de données

    text

    Alias
    UMLS CUI [1,1]
    C0919624 (Pregnancy of partner)
    UMLS CUI [1,2]
    C0347984 (During)
    SNOMED
    371881003
    UMLS CUI [1,3]
    C0008972 (Clinical Research)
    Retour au début de la page

    Similar models

    Pregnancy Information

    1 Formulaires
    1. StudyEvent: ODM
      1. Pregnancy Information
    Name
    Type
    Description | Question | Decode (Coded Value)
    Type de données
    Alias
    Item Group
    Pregnancy Information
    C0032961 (UMLS CUI-1)
    C1533716 (UMLS CUI-2)
    Item
    Did a female partner of the male subject become pregnant during the study?
    text
    C0919624 (UMLS CUI [1,1])
    C0347984 (UMLS CUI [1,2])
    C0008972 (UMLS CUI [1,3])
    Pregnancy of Partner, During, Clinical research
    Code List
    Did a female partner of the male subject become pregnant during the study?
    CL Item
    Yes (Yes)
    CL Item
    No (No)
    CL Item
    Not Applicable (Not Applicable)
    Retour au début de la page 

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