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A clinical study on the efficacy and safety of cutting seton and drainage therapy in the treatment of high perianal abscess

Phase 1
Conditions
High Prianal Abscess
Registration Number
ITMCTR2100005098
Lead Sponsor
China-Japan Friendship Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

1. Aged 18 to 65 years, male or female;
2. Diagnosed by digital examination and anorectal B-ultrasound, it was confirmed as high perianal abscess;
3. No history of perianal abscess surgery and abnormal anal morphology and function;
4. Patients voluntarily participated in clinical trials, signed informed consent, and were able to cooperate with clinical follow-up.

Exclusion Criteria

1. Patients with severe heart, lung, brain, liver and kidney diseases;
2. Pregnant or planning pregnancy and lactating women;
3. The doctor determines that other medical history has an impact on anal function;
4. Others due to religious ethnicity, diabetes, cancer, intestinal tuberculosis, Crohn's disease, AIDS;
5. Allergic constitution or allergic to the drugs used after surgery.

Study & Design

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