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A multicenter, double-blind, double-dummy, randomized controlled trial of the Chinese herbal medicine Linggui granule for patients with asthenospermia

Not Applicable
Recruiting
Conditions
asthenospermia
Registration Number
ITMCTR2200005858
Lead Sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, China
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

(1) Study participants must meet the diagnostic criteria of male infertility.
(2) Study participants must meet the diagnostic criteria of AZS.
(3) Men aged 22 to 45 years
(4) The participant must sign informed consent forms

Exclusion Criteria

(1)with infertility caused by organic lesions of the reproductive system
(2)with infertility caused by the inability to complete sexual intercourse, including but not limited to erectile dysfunction, ejaculatory disorder
(3)with reproductive system infection, such as chlamydia trachomatis or mycoplasma infection
(4)with abnormal sex hormone
(5)with palpable varicocele
(6)with a history of allergy to any medicine or ingredients used in this study
(7)complicated with mental diseases, malignant tumors, or serious organic diseases
(8)use drugs affecting the experimental study within 3 months

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
PR sperm rate;
Secondary Outcome Measures
NameTimeMethod
PR+NP sperm rate;spouse pregnancy rate;total effective sperm count;sperm DNA fragmentation index;
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