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Clinical Observation of TROPIS plus Surgery for the Treatment of Trans?sphincteric fistula

Clinical Observation of TROPIS plus Surgery for the Treatment of Trans?sphincteric fistula

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088135
Enrollment
Unknown
Registered
2024-08-12
Start date
2024-08-12
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Trans?sphincteric fistula

Interventions

Experimental group:perform TROPIS-Plug surgery
control group:perform TROPIS surgery

Sponsors

Yueyang Integrated Traditional Chinese and Western Medicine Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients who meet the diagnostic criteria for Trans?sphincteric fistula type and plan to undergo anal fistula surgery in our hospital's proctology department; (2) Age = 18 years old and = 65 years old, gender not limited; (3) Understand and agree to participate in this study and sign the informed consent form for surgery.

Exclusion criteria

Exclusion criteria: (1) Individuals with a history of colorectal surgery and those with congenital abnormalities in anal morphology and function (2) Patients with other anal and rectal diseases, such as anal fissure, rectal prolapse, genital warts, purulent sweat gland inflammation, perianal necrotizing fasciitis, etc (3) Merge patients with severe cardiovascular and cerebrovascular diseases, malignant tumors, and other systemic diseases (4) Patients with metabolic system diseases such as diabetes that may affect wound healing (5) Individuals with a history of alcohol or drug abuse (6) Pregnant, preconception, and breastfeeding patients (7) Patients with accompanying mental illnesses (8) Patients who have participated or are currently participating in other studies within one month prior to enrollment.

Design outcomes

Primary

MeasureTime frame
cure rate;

Secondary

MeasureTime frame
Wound pain condition;Anal function;Time for complete wound healing;

Countries

China

Contacts

Public ContactZhenyi Wang

Yueyang Integrated Traditional Chinese and Western Medicine Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

drxinhuo@163.com+86 136 0176 0317

Outcome results

None listed

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