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A Prospective Evaluation of Hemorrhoidal Surgery Outcome in Istanbul

M

Medipol Health Group

Status

Enrolling

Conditions

Indication, Unlabeled
Complication of Treatment
Quality of Life
Hemorrhoids

Treatments

Procedure: Hemorrhoidal surgery

Study type

Observational

Funder types

Other

Identifiers

NCT05429060
E-10840098-772.02-109

Details and patient eligibility

About

This study aims to evaluate the effect of surgical treatments on the quality of life in hemorrhoidal disease. All available treatment methods will be included in this 1-year cohort which is going to collect data from a big metropol.

Enrollment

2,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Surgical interventions under local and/or general anesthesia
  • Elective or emergency interventions (including thrombectomy)
  • Surgical interventions in operation room or office
  • Any kind of excision, sclerotherapy, ligation, suturation, ablation, mucopexy

Exclusion criteria

  • Any accompanying perianal disease (anal fistula, anal fissure, perianal abscess, anal condyloma extending into the anal canal)
  • Previous surgery for hemorrhoids (any intervention other than medical treatment)
  • Previous perianal surgery (internal sphincterotomy, fistula surgery)
  • Pelvic and/or perineal radiotherapy
  • Previous obstetric or perianal injury and/or sphincter repair
  • Previous rectal surgery (distal colectomy for benign or malignant etiology)

Trial contacts and locations

1

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Central trial contact

Naciye Cigdem Arslan, MD

Data sourced from clinicaltrials.gov

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