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Clinical study on prevention and treatment of moderate-severe pain during hemorrhoid operation

Clinical study on prevention and treatment of moderate-severe pain during hemorrhoid operation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000594
Enrollment
Unknown
Registered
2024-10-22
Start date
2023-05-29
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

mixed hemorrhoids

Interventions

Surgery group:Transverse division and longitudinal ligation + lactulose
TCM group:External stripping and internal ligature + Runchang Zhitong Powder
control group:External stripping and internal ligature + lactulose
Surgery+TCM group:Transverse division and longitudinal ligation + Runchang Zhitong Powder

Sponsors

China-japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) According to the diagnostic criteria of annular mixed hemorrhoids in the Chinese Medicine Industry Standard of the People's Republic of China on the basis of the establishment of the diagnosis of mixed hemorrhoids any of the following items can be diagnosed as annular hemorrhoids: a. The perianal hemorrhoids were distributed in 360° pananal canal. b. The anal canal is completely turned down with a toothed line moving down accordingly; c. The hemorrhoids show circular swelling or prolapse during stool. 2) Aged 18-60 years old first anal surgery. 3) It can tolerate surgical treatment and has no obvious contraindications. 4) Voluntarily undergo surgical treatment and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) ASA Grade IV patients and emergency surgery patients. 2) Under 18 years old or over 61 years old. 3) Patients with liver kidney cardiovascular and cerebrovascular diseases or tumors malnutrition endocrine and hematopoietic system and other serious primary diseases. 4) Patients with chronic diseases such as inflammatory bowel disease and tuberculosis. 5) Pregnant or lactating women and those who have mental illness or other reasons can not cooperate with surgical treatment. 6) People who are allergic or allergic to related drugs.

Design outcomes

Primary

MeasureTime frame
Anal function assessment;Evaluation of analgesic efficacy;Wound healing duration;Degree of anal stenosis;

Secondary

MeasureTime frame
Anal edema;Anal distention;stool appearance;Anal pain score;Defecation frequency;Follow-up recurrence;

Countries

China

Contacts

Public ContactWang Yanmei

China-Japan Friendship Hospital

wym003@163.com13311563388

Outcome results

None listed

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