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Randomized controlled study on the effect of Toupusan combined with new liquid dressing on wound healing after surgery for multiple drug-resistant perianal abscess

Study on the Wound Healing of Multi-drug Resistant Perianal Abscess with Toupansan Combined with New Liquid Dressing

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002497
Enrollment
Unknown
Registered
2025-12-24
Start date
2025-01-01
Completion date
Unknown
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multidrug-Resistant Perianal Abscesses

Interventions

Combination group:Oral Tounongsan +EXternal liquid dressing
Liquid Dressing group:EXternal liquid dressing
Tounongsan group:Oral Tounongsan
Control group:EXternal Vaseline Gauze Strip

Sponsors

The Second Affiliated Hospital of Hunan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1). According to the "Twelfth Five-Year Plan" textbook "Science of Anorectal Diseases" published by Tsinghua University Press, the clinical diagnosis guidelines for perianal abscess, anal fistula and rectovaginal fistula of the American Society of Colon and Rectal Surgeons [1], and the three-dimensional color Doppler ultrasound diagnosis of the Second Affiliated Hospital of Hunan University of Chinese Medicine, patients meeting the diagnostic criteria for acute purulent perianal abscess at the low position and with multiple drug-resistant bacterial infection confirmed by pus bacterial culture and drug sensitivity test in the laboratory of the Second Affiliated Hospital of Hunan University of Chinese Medicine are included. (2). Patients aged between 18 and 60 years old. (3). Patients without clear surgical contraindications all undergo one-time radical surgery for perianal abscess. (4). Patients without blood diseases, diabetes, tuberculosis, inflammatory bowel disease or other major underlying diseases. (5). Patients who voluntarily participate in the clinical research and sign the informed consent form (see the attachment). (6). Patients without a history of perianal surgery. (7). Those with normal morphology and function of the anus.

Exclusion criteria

Exclusion criteria: (1). Those with complex or high-positioned perianal abscesses discovered during the operation; (2). Those with major underlying diseases such as heart, brain, liver or kidney diseases; (3). Those with other anorectal diseases: such as circumferential mixed hemorrhoids, anal fissures, malignant tumors in the anal area, severe perianal skin diseases, inflammatory bowel diseases, etc.; (4). Patients with mental or psychological disorders; (5). Those with infectious diseases such as AIDS, syphilis, or condyloma acuminatum; (6). Those with diseases that affect wound healing: such as diabetes, tuberculosis, malignant tumors, hyperthyroidism, malnutrition or heavy smokers; (7). Pregnant and lactating women, and women during menstruation; (8). Those allergic to the study drug.

Design outcomes

Primary

MeasureTime frame
The rate of wound healing;

Secondary

MeasureTime frame
Wound pain rating;Wound exudate scoring;Wound healing time;wound healing-related growth factors:;inflammatory factors;oxidative stress indicators;

Countries

China

Contacts

Public ContactLiao Pan

The Second Affiliated Hospital of Hunan University of Chinese Medicine

598939391@qq.com15116406346

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026