MedPath

effect of clove in premature ejaculatio

Phase 2
Completed
Conditions
premature ejaculation.
Premature ejaculation
Registration Number
IRCT2016013126298N1
Lead Sponsor
Vice chancellor for research, Shahed University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Male
Target Recruitment
50
Inclusion Criteria

monogamous and heterosexual 18-40 years old man; Intravaginal ejaculation latency time less than 1 minutes; PEDT (Premature ejaculation diagnostic tool) questionnaire score more than eight
Exclusion criteria: History of severe or debilitating disease; diabetes; cardiac disease; liver disease; mental disease; thyroid dysfunction; addiction to any drugs or substances; pregnancy of wife; history of hypersensitivity to clove

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ejaculation latency time. Timepoint: 4 weeks before intervention and 2 months during it, 10 minutes before intercourse. Method of measurement: stopwatch.
Secondary Outcome Measures
NameTimeMethod
Premature ejaculation diagnostic tool questionnaire score. Timepoint: Before and after study. Method of measurement: Questionnaire.
© Copyright 2025. All Rights Reserved by MedPath