Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06175325

Trans-radial Superior Rectal Artery Embolisation for Haemorrhoids

Led by University Hospitals of North Midlands NHS Trust · Updated on 2025-09-03

20

Participants Needed

1

Research Sites

71 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Endovascular embolisation is already a common procedure for bleeding haemorrhoids in the acute setting, where surgical options are not possible or have been exhausted. This pilot study aims to add to the small body of evidence that transarterial embolisation of symptomatic haemorrhoids is also safe and effective in the elective setting, providing a good alternative to conventional surgical management. This is a day case procedure that is performed under local anaesthetic. For selected patients, this presents a less invasive management option with reduced potential morbidity. For a health care system under significant financial stress, this provides a potential means of cost improvement, the extent of which this study will try and quantify. A series of 20 selected patients will be recruited to undergo this procedure and then followed up for 24 months. The long-term goal of this pilot study is to form the basis of a national registry of such procedures.

CONDITIONS

Official Title

Trans-radial Superior Rectal Artery Embolisation for Haemorrhoids

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with grade II-IV haemorrhoid disease with recurrent or active bleeding
  • Patients who do not wish to undergo surgery for their symptoms
  • Patients with symptoms despite recent surgery
  • Patients willing and able to give fully informed consent
  • Patients aged 18 years or older
Not Eligible

You will not qualify if you...

  • Patients who are not otherwise fit for surgery
  • Patients with significant ano-rectal comorbidities such as cancer, fistula, or abscesses
  • Patients who are unable to sign the informed consent form
  • Patients who are pregnant
  • Patients with history of significant colorectal disease or previous colectomy
  • Patients with history of an allergic reaction to x-ray contrast
  • Patients currently involved in other research studies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Hospitals of North Midlands NHS Trust

Stoke-on-Trent, United Kingdom

Actively Recruiting

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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