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Clinical Trials/NCT07564791
NCT07564791CompletedNot Applicable

A Study to Evaluate the Effects of the Libido Lift Supplement on Libido and Sexual Desire in Men

Bio Nature Health1 site in 1 country60 target enrollmentStarted: March 27, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
60
Locations
1
Primary Endpoint
Change in Libido and Sexual Desire Score

Study Overview

Brief Summary

This study evaluates the effects of the Libido Lift supplement on libido and sexual desire in men aged 35-75 years. Participants will be randomized to receive either the supplement or placebo for 4 weeks, with outcomes assessed באמצעות questionnaires at multiple timepoints.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Care Provider, Outcomes Assessor)

Eligibility Criteria

Ages
35 Years to 75 Years (Adult, Older Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Aged 35-75 years
  • Low sexual desire or desire to improve libido
  • Dissatisfaction with sex life or desire to improve intimacy
  • Desire to improve energy, endurance, stamina
  • Sexually active (≥2 times per week)
  • Willing to comply with study requirements
  • Generally healthy
  • Resides in the United States

Exclusion Criteria

  • Recent surgery or major illness
  • Heavy alcohol use
  • Hormone-related medications
  • Liver disease or hypertension
  • Use of anticoagulants
  • Allergies to ingredients
  • Chronic conditions affecting participation
  • Participation in another study
  • History of substance abuse

Arms & Interventions

Libido Lift Supplement

Experimental

Participants receive Libido Lift supplement daily for 4 weeks.

Intervention: Dietary Supplement: Libido Lift (Dietary Supplement)

: Placebo

Placebo Comparator

Participants receive placebo capsules daily for 4 weeks.

Intervention: Placebo (Dietary Supplement)

Outcomes

Primary Outcomes

Change in Libido and Sexual Desire Score

Time Frame: Baseline, Week 1, Week 2, Week 3, Week 4

Libido and sexual desire will be assessed using study-specific self-reported questionnaires. Questionnaire responses will be used to generate a score reflecting participants' level of libido and sexual desire. Changes in scores over time will be used to evaluate the effect of the intervention. Higher scores indicate greater libido and sexual desire.

Secondary Outcomes

  • Change in Self-Reported Sexual Satisfaction(Baseline, Week 1, Week 2, Week 3, Week 4)
  • Change in Self-Reported Intimacy(Baseline, Week 1, Week 2, Week 3, Week 4)
  • Change in Self-Reported Energy Levels(Baseline, Week 1, Week 2, Week 3, Week 4)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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