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Clinical Study to Reduce Premature Ejaculation in Healthy Adult Men

NCT06571318 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-08-26

No results posted yet for this study

Summary

The current study focuses on clinical validation of efficacy of nutraceutical product in management of male health. In healthy adult men with induced premature ejaculation, the introduction of these nutraceuticals has been associated with notable improvements in quality of life. These supplements help them for enhanced sexual satisfaction, increased control over ejaculation, and a reduction in performance anxiety. The psychological benefits are significant, as the improvement in sexual function can lead to higher self-confidence and a more positive outlook on life.

Conditions

  • Premature Ejaculation
  • Stress

Interventions

OTHER

Destress and Perform Capsule-U001

Two Capsules in sequence daily after meal for 60 days.

OTHER

Destress and Perform Capsule-I001

Two Capsules in sequence daily after meal for 60 days.

OTHER

Placebo capsules 002

Two Capsules in sequence daily after meal for 60 days

Sponsors & Collaborators

  • Herbolab India Pvt. Ltd.

    lead INDUSTRY

Principal Investigators

  • Dr. Ramshyam Agarwal, MBBS, DNB · Lokmanya Medical Research Centre and Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
21 Years
Max Age
50 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-09-05
Primary Completion
2024-11-20
Completion
2024-12-28

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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 NCT06571318 on ClinicalTrials.gov