Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06339996

Male Supplements for Sperm Quality and Aging

To Investigate Supplements for Improving Male Sperm Quality and Combating Aging

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Kaohsiung Veterans General Hospital. · Academic / Other
Sex
Male
Age
30 Years – 50 Years
Healthy volunteers
Accepted

Summary

This study investigates the effects of a new supplement on sperm quality in men with poor sperm quality. Fifty patients will receive the supplement for three months, followed by semen analysis and assessment of sperm aging and mitochondrial function. Changes in sexual function and aging symptoms will also be evaluated.

Detailed description

Due to modern lifestyle factors such as high work pressure, stressful routines, and environmental pollution, there has been a significant decline in sperm quality among men, potentially leading to infertility. In response, various supplements have emerged claiming to enhance sperm quality. This prospective investigation aims to determine the efficacy of a new supplement in improving sperm quality among patients with poor sperm quality. The study will enroll 50 patients undergoing semen analysis at our reproductive center, administering the supplement over a three-month treatment period to those identified with poor sperm quality. Subsequent semen analysis will be conducted, alongside assessments of sperm mitochondrial metabolic function before and after supplement administration. Sexual function and aging symptoms will also be evaluated using the International Index of Erectile Function (IIEF-5) and the Aging Males Symptoms Scale (AMS) before and after the supplementation period. The study aims to compare differences in semen analysis, sperm mitochondrial metabolic function, sexual function, and aging symptoms before and after supplementation.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTMale supplementParticipants will be administered supplements for a three-month treatment period

Timeline

Start date
2024-03-26
Primary completion
2025-10-31
Completion
2025-12-31
First posted
2024-04-01
Last updated
2024-08-02

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT06339996. Inclusion in this directory is not an endorsement.