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Clinical Study of Guangsi Yulin Decoction's Effect on Sperm DNA Fragmentation Index of asthenospermia patients

Phase 1
Conditions
Asthenospermia
Registration Number
ITMCTR2000004121
Lead Sponsor
Dongzhimen Hospital, Beijing University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

(1) Meet the western medical diagnostic criteria of male infertility and asthenospermia, and have the two diagnoses at the same time;
(2) TCM syndrome differentiation conforms to kidney deficiency syndrome;
(3) Male aged 22 to 45 years;
(4) Married, husband and wife have a harmonious family relationship;
(5) Sperm DNA fragmentation index (DFI) >=30%;
(6) No other organic lesions of the reproductive system;
(7) Those who did not receive treatment with similar drugs or other therapies within 2 weeks before the study;
(8) Understand the content of the study and sign the informed consent.
Those who meet the above 8 criteria at the same time will be included in the study; otherwise, they will not be included

Exclusion Criteria

(1) According to the Manual of Human Semen Examination and Treatment Laboratory, edition 5, except for total sperm motility < 40% and forward motility < 32%, there are other abnormalities in semen examination;
(2) Patients with a family history of genetic diseases;
(3) Suffering from varicocele, prostatitis and other diseases that lead to sperm quality decline;
(4) Patients with active infection;
(5) Patients with severe primary diseases such as cardiovascular, liver, kidney and hematopoietic system;
(6) Patients with mental disorders;
(7) Patients who have a long-term and large amount of smoking and drinking habits, or are exposed to high temperature, radiation and toxic chemical environment, but cannot change or give up;
(8) Allergic constitution and allergic to multiple drugs.
Meeting any of the above is considered as meeting the exclusion criteria, and exclusion is required.Those who meet the above 8 criteria at the same time will be included in the study; otherwise, they will not be included

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Semen routine;
Secondary Outcome Measures
NameTimeMethod
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