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Clinical Trial to Investigate the Effectiveness of a Dietary Supplement in Increasing Libido and Sexual Function in Postmenopausal Women.

NCT03820453 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2019-01-29

No results posted yet for this study

Summary

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).

Conditions

  • Female Sexual Arousal Disorder

Interventions

DIETARY_SUPPLEMENT

Tribulus Terrestris

The experimental arm will receive a dietary supplement to increase the libido and sexual function

OTHER

Placebo treatment

The control arm will receive a placebo product with similar organoleptic qualities and the same posology characteristics

Sponsors & Collaborators

  • Analysis and Research Network, S.L

    collaborator OTHER

  • Kern Pharma, S.L.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
45 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-29
Primary Completion
2019-08-29
Completion
2019-08-29

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03820453 on ClinicalTrials.gov