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Clinical Trial Summary

This study is a prospective, multicentre, and randomized-controlled clinical study.The researchers wanted to explore the optimal treatment regimen for soft hemorrhoid within I-Ⅲ degrees by evaluating and comparing the effectiveness, safety and cost effect ratio of sclerosing injection and rubber lap ligation in patients with different internal hemorrhoid scores


Clinical Trial Description

From November 2021 to July 2022, patients with internal hemorrhoids seeking treatment were enrolled according to the following criteria: 1. Age 18 to 75, men and women; 2. Patients with clinical symptoms of degree I-Ⅲ internal hemorrhoids confirmed after medical history collection, clinical examination or colonoscopy; 3. The patient was willing to receive minimally invasive treatment for internal hemorrhoids and sign informed consent by himself or his legal agent. Exclusion criteria are as follows: 1. age <18 or> 75; 2. External hemorrhoids or mixed hemorrhoids; 3. Ⅳ degree of hemorrhoid 4. Unsymptomatic internal hemorrhoids; 5. Internal hemorrhoids were combined with complications such as chimerism, thrombosis, ulceration, or infection; 6. Poor basic conditions can not tolerate endoscopic treatment, such as serious cardiovascular and cerebrovascular diseases, respiratory dysfunction, liver and kidney failure, mental disorders, etc.; 7. There are other serious diseases involving the rectum and anus, such as anal fistula, perianal infection, anal stenosis, inflammatory bowel disease activity period, colorectal tumors, etc.; 8. Patients with severe coagulation dysfunction or long-term oral anticoagulant drugs or antiplatelet aggregation drugs without withdrawal; 9. Women in pregnancy or puerperium; 10. Sclerotic with allergy patient , such as polycininol, etc; 11. Previous history of endoscopic treatment of hemorrhoid disease, surgical history or other low rectal and anal surgery history; 12. The patient was unwilling to receive endoscopic treatment for internal hemorrhoids, and himself or his legal agent refused to sign the informed consent form. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05089500
Study type Interventional
Source Renmin Hospital of Wuhan University
Contact Mingkai Chen, M.D
Phone 0086-13720330580
Email kaimingchen@163.com
Status Not yet recruiting
Phase N/A
Start date November 1, 2021
Completion date September 30, 2023

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