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Multicentre, Randomised, Double-blind, Placebo-controlled, Parallel-group Clinical Trial to Investigate the Effectiveness of a Dietary Supplement in Increasing Libido and Sexual Function in Postmenopausal Women.
This clinical Trial will assess the effects of a dietary supplement based on Tribulus terrestris on the libido and sexual function in postmenopausal women, by doing a follow up of the FSFI scale and different variables during 3 months period. Participants will be allocated to dietary supplement or placebo, and will attend to 3 visits (baseline, 6 weeks, 12 weeks and at 24 weeks optional).
Age
45 - 65 years
Sex
FEMALE
Healthy Volunteers
No
CAP Manso
Barcelona, Spain
Fundació Puigvert
Barcelona, Spain
Hospital Clínic, Barcelona
Barcelona, Spain
Sexology Institute
Barcelona, Spain
Start Date
October 29, 2018
Primary Completion Date
August 29, 2019
Completion Date
August 29, 2019
Last Updated
January 29, 2019
110
ESTIMATED participants
Tribulus Terrestris
DIETARY_SUPPLEMENT
Placebo treatment
OTHER
Lead Sponsor
Kern Pharma, S.L.
Collaborators
NCT06116045
NCT06651541
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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