HAL-RAR Versus Hemorrhoidectomy in the Treatment of Grade III-IV Hemorrhoids. Prospective, Randomized Trial
Hemorrhoids, Pain, Postoperative
About this trial
This is an interventional treatment trial for Hemorrhoids focused on measuring HAL-RAR, Hemorrhoids, Hemorrhoid artery ligation, Anal repair, Quality of Life, Postoperative Complications
Eligibility Criteria
Inclusion Criteria:
- Patients with symptomatic grade III or IV hemorrhoids (bleeding, pain, itching, soiling or prolapse) that are elegible for surgical treatment with both methods.
Exclusion Criteria:
- Associated recto-anal pathology such as acute thrombosed hemorrhoid, anal fissure, perianal fistula, perianal abscess, rectal prolapse, fecal incontinence or anal stenosis.
- Prior anorectal surgery .
- Systemic pathology that could alter the outcome of the surgery as coagulopathies, chronic pain with continued consumption of analgesics.
- Age younger than 18 or older than 80 years, socio-pathology or inability to understand the study objectives
Sites / Locations
- Hospital Plató
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Hemorrhoidectomy
HAL-RAR
Open hemorrhoidectomy may include one to three anal cushions and made according to the Milligan-Morgan technique, with resection of the anal cushion and the external hemorrhoidal epidermal component using electrocautery and ligation of the hemorrhoidal base with absorbable suture
Hemorrhoidal artery ligation and rectoanal repair will be performed with the AMI minimally invasive surgery device HAL/RAR, and consist in the ligation of the terminal branches of the superior rectal artery with 2-0 absorbable polyglycolic acid suture after identifying the blood flow approximately 3 cm above the dentate line by using Doppler guidance. Subsequently, a running suture was added from the suture point to 5 mm above the dentate line to lift the prolapsing hemorrhoid. Other procedures will not be associated.