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A single-center study on the treatment of hemorrhagic internal hemorrhoids with endoscopic sclerotherapy and classic hemorrhoidectomy based on LrDRf classification

A single-center study on the treatment of hemorrhagic internal hemorrhoids with endoscopic sclerotherapy and classic hemorrhoidectomy based on LrDRf classification

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087765
Enrollment
Unknown
Registered
2024-08-04
Start date
2024-08-04
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

hemorrhagic internal hemorrhoids

Interventions

Experimental group:Endoscopic sclerotherapy
Control group:Traditional hemorrhoidectomy

Sponsors

The Second People's Hospital of Yibin
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 18-75 years old; (2) Patients with hemorrhagic internal hemorrhoids accompanied by related symptoms, who meet the LrD0.1~Rf0-2 or LrDRf1-2 classification and have not responded to conservative treatments such as medication (with D > 1mm); (3) Elderly patients, those with hypertension, diabetes, or severe systemic diseases who are unable to tolerate surgical procedures; (4) Patients who have not undergone hemorrhoid procedures and/or hemorrhoid surgery before; (5) Voluntarily sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Mixed hemorrhoids and external hemorrhoids; (2) Hemorrhagic internal hemorrhoids accompanied by complications such as incarceration, thrombosis, ulceration, infection, etc.; (3) Severe heart, brain, lung, liver, or kidney failure that cannot tolerate endoscopic treatment; (4) Patients with perianal infectious diseases, anal fistula, history of radiation therapy, or active inflammatory bowel disease; (5) Patients with rectal tumors; (6) Pregnant or postpartum women; (7) Patients with a history of mental illness; (8) Allergy to sclerosing agents; (9) Incomplete clinical data; (10) Patients who have been receiving long-term anticoagulation therapy; (11) Patients with less than 6 months of follow-up time; (12) Abnormal coagulation function, platelet function, or platelet count; (13) Patients or their families who do not consent to endoscopic sclerotherapy for hemorrhoids or participation in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Overall efficacy;Postoperative pain;Anal function;Quality of life;C-reactive protein, CRP;

Secondary

MeasureTime frame
Surgery duration and intraoperative bleeding;Postoperative complications;Length of hospital stay;

Countries

China

Contacts

Public ContactMiao Wu; Cairong Hu

The Second People's Hospital of Yibin

13990905852@163.com+86 139 9090 5852

Outcome results

None listed

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