MedTrace Logo

Trial of Latex Vs Non-latex Hemorrhoid Banding

NCT06625138 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 164

Last updated 2024-10-28

No results posted yet for this study

Summary

This study will involve the recruitment of adult patients with hemorrhoids for whom rubber band ligation is the recommended treatment. Patients will be randomized to receive banding with a latex band or non-latex band. Our goal will be to measure the performance of latex bands vs non-latex bands.

Conditions

  • Hemorrhoid
  • Hemorrhoid Bleeding

Interventions

DEVICE

Latex Band

Hemorrhoid banding with latex band

DEVICE

Non-Latex Band

Hemorrhoid banding with non-latex bands

Sponsors & Collaborators

  • Huntington Memorial Hospital

    lead OTHER

Principal Investigators

  • Adam Truong, MD · Huntington Health

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-30
Primary Completion
2025-10-01
Completion
2026-10-01
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06625138 on ClinicalTrials.gov