About this trial
This single-center prospective observational study aims to evaluate clinical outcomes, postoperative pain scores, complications, and patient satisfaction in adults undergoing laser hemorrhoidoplasty for symptomatic internal hemorrhoidal disease. Additional objectives are to assess the relationship between hemorrhoid stage, dominant presenting symptoms, operative technical details, and postoperative outcomes. No study-specific intervention beyond routine clinical care and follow-up will be performed.
Eligibility criteria
Qualifiers
Age 18 years or older
Symptomatic internal hemorrhoidal disease
Scheduled to undergo laser hemorrhoidoplasty
Willingness to participate and provision of informed consent
Disqualifiers
Grade IV hemorrhoidal disease
Acute thrombosed hemorrhoids
Additional anorectal pathology such as anal fissure, fistula, or perianal abscess
History of inflammatory bowel disease or colorectal malignancy
Trial design
Treatments tested in this trial
- Laser Hemorrhoidoplasty