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Clinical Trials in the USA / NCT07635784
Recruiting Observational

Prospective HemorrhoIdaL EmboliSation (PILES) Registry

NCT07635784 · tracked via the Priya Life Science USA tracker
Sponsor
Joint & Vascular Institute
Phase
Observational
Started
2026-01-18
Last updated
2026-06-12

Condition(s) studied

HemorrhoidInternal HemorrhoidsHemorrhoid BleedingHemorrhoidal BleedingInternal Hemorrhoid

Investigational drug(s) / intervention(s)

Hemorrhoid Artery Embolization

Hemorrhoid Artery Embolization: Hemorrhoidal Artery Embolization (HAE)-often referred to clinically as the Emborrhoid technique-is a minimally invasive, image-guided procedure in which embolic agents are delivered into the superior rectal arteries to reduce hypervascular blood flow, thereby shrinking engorged hemorrhoidal plexuses and alleviating chronic bleeding and discomfort from internal hemorrhoids.

Study summary

The goal of this observational study (prospective registry) is to collect long-term real-world data on the effectiveness and safety of hemorrhoid artery embolization (HAE) for symptomatic bleeding internal hemorrhoids in adults aged 18 years or older that have not responded to medical therapy.

The main question it aims to answer are:

1\) Does HAE lead to sustained improvement in bleeding (HDSS scores over 12-36 months?

Participants will:

* Undergo HAE as part of their routine clinical care.
* Complete clinical follow-up assessments at 1, 3, 6, 12, 18, 24, and 36 months after treatment, including symptom and quality-of-life questionnaires.
* Have safety outcomes tracked according to Society of Interventional Radiology guidelines.

There is no comparison group; results will be analyzed to identify predictors of success and inform best practices for patient selection and treatment.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (≥18 years) with symptomatic bleeding internal hemorrhoids refractory to medical therapy, referred for HAE. Exclusion Criteria: * Pregnancy, coagulopathy, severe comorbidities, or inability to consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Joint and Vascular Institute Libertyville Illinois Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07635784 on ClinicalTrials.gov ↗ ← All trials in the USA