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NOT YET RECRUITING
NCT07866248
PHASE4

Evaluation of Polidocanol Foam Sclerotherapy in Symptomatic Internal Hemorrhoids: A Prospective Study

Sponsor: Radwa Hussein Mohammed Hasanen

View on ClinicalTrials.gov

Summary

To evaluate the efficacy, durability, safety, and clinical/endoscopic outcomes of standardized 3% polidocanol foam sclerotherapy in patients with symptomatic grade II-III internal hemorrhoids over a 12-month follow-up period.

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

130

Start Date

2026-10-01

Completion Date

2028-09-01

Last Updated

2026-10-08

Healthy Volunteers

No

Interventions

PROCEDURE

Standardized 3% Polidocanol Foam Sclerotherapy

3% polidocanol foam, Sims position, Open-ended anoscope, use of 20-G needle, Injection above dentate line, Intra-pile injection, 2 ml foam / symptomatic hemorrhoidal cushion, Maximum 3 cushions / session, Maximum plained study dose 6 ml foam / session , Assessment at 4 weeks