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A study to evaluate the efficacy of Investigational Drug M. Libido, in Enhancing Testosterone Level and Improving Sperm Profile in Male Volunteers

Not Applicable
Registration Number
CTRI/2019/01/016876
Lead Sponsor
Aurea Biolabs Pvt Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

1.Male subjects of age range between 21-55 years olds

2.Healthy heterosexual males interested in increasing libido

3.Committed sexual relationship for at least 6 months

4.Sexually active for the last 6 months

5.Stable, sexual relationship for the duration of the study

6.Total testosterone levels within the healthy reference range (Endocrine Society) at screening (264 - 916 ng/dL) â?? could target men at lower end of the healthy testosterone range (low normal).

Exclusion Criteria

•Allergy or intolerance to study ingredients

•Any physical unavailability to sexual partner during duration of study

•Any physical disability that limits sexual function

•Treatment or therapy for sexual disorder during the last 6 months

•Prescribed medication for anticoagulation therapy.

•Diagnosed with any medical disorders or diseases such as severe renal/hepatic insufficiency, psychiatric disorders, prostatic cancer or benign hypertrophy, acute genitourinary disorder or any other conditions that identify the subject as unhealthy for the study or interfere with any study parameters.

•Diagnosed with hypertension and receiving medications for hypertension

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Change in serum levels of total and free testosterone levels <br/ ><br>2.Change in sexual function: International Index of Erectile Dysfunction (IIEF) <br/ ><br>3.Change in Quality of Life: SF-36 questionnaire <br/ ><br>Timepoint: week 4 week 8 and week 12
Secondary Outcome Measures
NameTimeMethod
Change from baseline in hematology and biochemistry parameters between treatmentsTimepoint: week 4 week 8 and week 12
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