Laser Hemorrhoidoplasty: Laser-based minimally invasive treatment of internal hemorrhoidal disease performed as part of routine clinical care.
Study summary
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
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age 18 years or older
* Symptomatic internal hemorrhoidal disease
* Scheduled to undergo laser hemorrhoidoplasty
* Willingness to participate and provision of informed consent
Exclusion Criteria:
* 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
* Previous major anal surgery'
Primary outcome measure(s)
Postoperative pain score — At 6 hours, 24 hours, and 1 week after surgery Postoperative pain assessed using a 0 to 10 Visual Analog Scale (VAS), where 0 indicates no pain and 10 indicates the worst imaginable pain; higher scores indicate worse pain.
Trial sites (1)
Facility
City
Region
Status
Sanliurfa Education and Research Hospital
Sanliurfa
Şanlıurfa
Recruiting
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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