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Effect of modified TROPIS on satisfaction of patients with high anal fistula

Effect of modified TROPIS on satisfaction of patients with high anal fistula

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066929
Enrollment
Unknown
Registered
2022-12-21
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

high anal fistula

Interventions

control group:incision and thread hanging surgery

Sponsors

Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. It conforms to the diagnostic criteria of high anal fistula in China Expert Consensus on the Diagnosis and Treatment of Anal Fistula (2020 edition) formulated by the Clinical Guidelines Working Committee of Anorectal Physician Branch of Chinese Medical Association, and the lesions involve > 30% of external sphincter. 2. Patients who have not received surgical treatment after rectal ultrasound or pelvic MR plain scan, or who only underwent incision and drainage at the initial perianal abscess stage. 3. Age =18, male or female. 4. According to Wexner score, anal function is normal. 5. Have the ability to understand Chinese and agree to participate in this research.

Exclusion criteria

Exclusion criteria: 1. Pre-operative impaired anal self-control, or those who had undergone radical surgery at the time of initial perianal abscess incision and drainage. 2. Other infectious diseases and associated enteritis (including concomitant perianal abscess, inflammatory bowel disease, anal canalitis, Crohn's disease, etc.). 3. Pregnant or lactating women, combined with diabetes mellitus, connective tissue disease or related metabolic diseases, without heart, lung, liver, kidney diseases and hemolytic diseases 4. patients with intellectual or mental disorders. 5. patients who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
cure rate;changes of anal function;patient satisfaction;

Secondary

MeasureTime frame
duration of surgery;at discharge;intraoperative blood loss;pain score;complications;

Countries

China

Contacts

Public ContactHou Yi

Nanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine

xunziyang2015@163.com13260765789

Outcome results

None listed

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