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Recruiting NCT07404774

NCT07404774 Hemorrhoid Suture Mucopexy Combined With Laser Hemorrhoidoplasty

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Clinical Trial Summary
NCT ID NCT07404774
Status Recruiting
Phase —
Sponsor National and Kapodistrian University of Athens
Condition Haemorrhoid
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2026-01-01
Primary Completion 2028-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL
Interventions
Laser Haemorrhoidoplasty and Suture Mucopexy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 100 participants in total. It began in 2026-01-01 with a primary completion date of 2028-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This prospective cohort study evaluates whether combining "suture mucopexy" (a simple stitch-based lift of prolapsed tissue) with Laser Hemorrhoidoplasty (LHP) can effectively relieve pain, bleeding and prolapse in adults with moderate-to-severe hemorrhoids (Grades II-IV). Participants will undergo the combined, non-Doppler-guided procedure and be followed for one year. The primary question is how long patients need post-operative pain medication and if they first experience complete symptom relief; secondary questions examine quality-of-life, safety (bleeding, urinary retention, stenosis) and the rate of hemorrhoid recurrence/re-operation.

Eligibility Criteria

Inclusion Criteria: * Adults (\>18 years). * Symptomatic Hemorrhoidal Disease (Goligher Grades II, III, IV). * Patients with or without recurrent disease after prior procedures (e.g., RBL, infrared coagulation, Milligan-Morgan, etc). Exclusion Criteria: * Acutely thrombosed hemorrhoids. * Concomitant anal fistula or abscess requiring separate surgical management. * IBD (Crohn's/Ulcerative Colitis) with active rectal involvement. * Previous Stapled Haemorrhoidopexy (SH/Longo).

Contact & Investigator

Central Contact

George Theodoropoulos

✉ georgetheocrs@live.com

📞 +30 213 208.8000

Frequently Asked Questions

Who can join the NCT07404774 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Haemorrhoid. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07404774 currently recruiting?

Yes, NCT07404774 is actively recruiting participants. Contact the research team at georgetheocrs@live.com for enrollment information.

Where is the NCT07404774 trial being conducted?

This trial is being conducted at Athens, Greece.

Who is sponsoring the NCT07404774 clinical trial?

NCT07404774 is sponsored by National and Kapodistrian University of Athens. The trial plans to enroll 100 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology