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Randomized, open, parallel controlled clinical study of Haiai Decoction combined with oral administration of finasteride for male androgenic alopecia

Phase 1
Conditions
androgenic alopecia
Registration Number
ITMCTR2000003332
Lead Sponsor
Shanghai Tongji Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

1. The typical clinical manifestations were in accordance with the diagnosis of AGA, and the degree of hair loss was in accordance with the BASP classification of androgenic hair loss;
2. In general, patients with good condition (no previous heart, systemic or scalp diseases) have not used any drugs that may affect hair growth (antihypertensive drugs, hormones, cytotoxic drugs, anti androgen drugs, etc.) within the first 3 months of the study;
3. Patients who agree to participate in observation and follow-up, are willing to receive follow-up, and can cooperate closely in the whole process.

Exclusion Criteria

1. Finasteride was taken orally 18 months before the start of the experiment;
2. Use local or systemic drugs that affect hair growth within 12 months;
3. History of hair transplantation;
4. Systemic or scalp diseases that may affect hair growth.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
P.Suchonwanit 7-point rating scale;
Secondary Outcome Measures
NameTimeMethod
Dermatology Life Quality Index;Evaluation of hair regeneration rate;Severity of Alopecia Tool, SALT;Measuring the thickness and density of hair with a dermatoscope;Using 4-point scale to evaluate patients' subjective satisfaction;
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