Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Sutureless hemorrhoidectomy vs conventional ligation for advanced hemorrhoids

Official title: Sutureless Hemorrhoidectomy Versus Conventional Ligation: A Comparative Prospective Randomized Clinical Trial

Run by Sohag University · NCT07824999 · Data updated 2026-11-12

This study tests whether a sutureless, energy-based hemorrhoidectomy can reduce pain and recovery time compared with the standard Milligan-Morgans procedure in adults with Grade III–IV hemorrhoids.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorSohag University
Academic / other
Locations1 site (Sohag)
StatusRecruiting
StartedOctober 1, 2026
Main results expectedApril 1, 2027
Study endsOctober 1, 2027
Registry record updatedSeptember 17, 2026
Trial IDNCT07824999 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18 or older with symptomatic Grade III–IV hemorrhoidal disease requiring excisional hemorrhoidectomy.

Probably not a fit

Patients with Grade I–II hemorrhoids, acute thrombosed external hemorrhoids, or other anorectal conditions may not benefit from this comparison.

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

What this trial studies

In this prospective randomized trial, adults with symptomatic Grade III–IV hemorrhoidal disease are assigned to either sutureless hemorrhoidectomy using an energy-based vessel sealing device or the conventional Milligan-Morgan ligation method. The study aims to compare perioperative and postoperative outcomes, including pain, bleeding, wound healing, complications, return to normal activities, and recurrence over a 6-month follow-up. Standardized analgesia and postoperative care are provided, with follow-ups at 1 week, 2 weeks, 1 month, 3 months, and 6 months. Conducted at Sohag University Hospital, the trial enrolls 50 participants (25 per arm) to determine if the sutureless approach offers advantages in recovery and safety. Outcomes will inform whether energy-based sutureless techniques can become preferred options for advanced hemorrhoidal surgery.

Why it matters

Potential benefit: If successful, patients could experience less postoperative pain, faster recovery, and fewer complications with a less invasive hemorrhoidectomy approach.

How similar studies have gone: Previous evidence supports the concept of energy-based, sutureless techniques reducing tissue trauma, but randomized data in advanced hemorrhoids remain limited, making this study relatively novel in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patients aged 18 years or older.
* Patients with symptomatic grade III or grade IV hemorrhoidal disease.
* Combined internal and external hemorrhoidal disease requiring excisional hemorrhoidectomy.
* Recurrent bleeding, prolapse, pain, mucous discharge, or hygiene difficulty despite conservative or office-based treatment.

Exclusion Criteria:

* Patients younger than 18 years.
* Grade I or grade II hemorrhoids suitable for conservative or office-based therapy.
* Acute thrombosed external hemorrhoids requiring emergency management.
* Associated anal fissure, fistula-in-ano, perianal abscess, or inflammatory bowel disease.
* Suspected or confirmed colorectal malignancy\[cite: 1\].
* History of previous anorectal surgery\[cite: 1\].
* Bleeding diathesis, uncontrolled anticoagulant therapy, or severe coagulopathy\[cite: 1\].

Where it's running

  • Sohag University Hospital, Department of General Surgery
    Sohag, Egypt
    Recruiting

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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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.