Comparing latex and non-latex bands for treating hemorrhoids

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study recruits adult patients with symptomatic grade 2-3 internal hemorrhoids who are candidates for rubber band ligation. Participants will be randomly assigned to receive either a latex band or a non-latex band for treatment. The primary goal is to evaluate the effectiveness of non-latex bands compared to latex bands, while also assessing any associated adverse effects such as pain and bleeding within three weeks post-treatment.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Symptomatic grade 2-3 internal hemorrhoids undergoing rubber band ligation

Exclusion Criteria:

* Previous hemorrhoidal banding within the past year
* Known latex allergy
* Pregnancy
* Anticoagulation use
* Bleeding disorder
* Portal hypertension
* Inflammatory bowel disease
* Immunosuppression
* Functional neurologic disorder
* Pelvic floor dysfunction
* Any records flagged "break the glass" or "research opt out".

Where it's running

• Huntington Memorial Hospital
  Pasadena, California, United States Recruiting

Study contacts

• Principal investigator: Adam Truong, MD — Huntington Health
• Study coordinator: Adam Truong, MD
• Email: adam.truong@huntingtonhealth.org
• Phone: (626) 397-5896

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.