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Maca Extract in Sexual Dysfunction Male

Effects of Lepidium Meyenii (Maca) Extract Supplementation on Male Sexual Funtion

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05891327
Enrollment
60
Registered
2023-06-06
Start date
2023-12-31
Completion date
2024-05-31
Last updated
2023-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sexual Dysfunction Male

Brief summary

The purpose of this study was to investigate the effects of Lepidium meyenii (Maca) extract supplementation on male sexual funtion.

Detailed description

All participants performed anthropometric measurements, blood collection and questionnaire survey at 0-week. A random, double-blind design will be used to assign 60 participants into the experimental group (n = 30) or placebo group (n = 30). All participants consumed either 2.25 g Lepidium meyenii (Maca) extract twice per day for 12 weeks. The anthropometric measurements, blood samples, and questionnaire survey were collected again at 6-week, 12-week, 16-week, and 24-week. Data will be analyzed by two-way mixed design ANOVA.

Interventions

DIETARY_SUPPLEMENTMaca

2.25 g Lepidium meyenii (Maca) extract twice per day for 12 weeks

DIETARY_SUPPLEMENTPlacebo

Placebo

Sponsors

Taipei Medical University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

A double-blind, matched-pair study design

Intervention model description

assign 60 participants into the experimental group (n = 30) or placebo group (n = 30)

Eligibility

Sex/Gender
MALE
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. evaluated as sexual dysfunction for more than three months by physician 2. international index of erectile function (IIEF) score is less than or equal to 21 3. erectile hardness score (EHS) score is less than or equal to 3 4. aged over 18 years old

Exclusion criteria

1. unable to cooperate with the course of the treatment 2. suffering from sexually transmitted diseases such as Syphilis, AIDS and HPVs 3. had Radical Prostatectomy (total removal of the prostate gland) 4. suffering from active tumors in the prostate or pelvic area 5. suffering from Hypogonadism 6. anatomical deformation of the penis 7. men with penile prosthesis 8. suffering from psychotic disorder (manic disorder, chronic depression, etc.) 9. suffering from neurological diseases (multiple sclerosis, brain or spinal cord injuries, etc.) 10. using Permanent pacemaker 11. considered unsuitable to participate in this experiment according to the doctor 12. alcohol or drug abuse

Design outcomes

Primary

MeasureTime frame
IIEF-5 scoreBaseline (before supplementation)
EHS scoreBaseline (before supplementation)
level of PSABaseline (before supplementation)
Testosterone levelBaseline (before supplementation)
LH levelBaseline (before supplementation)
Level of FSHBaseline (before supplementation)

Countries

Taiwan

Contacts

Primary ContactMing Ta Yang, Doctorate
yangrugby@tmu.edu.tw886-2-27361661

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026