A Trial of Closed Hemorrhoidectomy Under Local Perianal Block Versus Spinal Anesthesia

Not Applicable

Completed

• Conditions: Postoperative Pain; Complications; Satisfaction
• Interventions: Procedure: spinal block; Procedure: Perianal block

• Registration Number: NCT00925912
• Lead Sponsor: Phramongkutklao College of Medicine and Hospital

Brief Summary

Hemorrhoidectomy can be carried out under several modes of anesthesia. In western country hemorrhoidectomy usually be performed under general anesthesia, however there may be the complications resulted from general anesthesia together with associated diseases in advanced age, caudal or spinal anesthesia has been used as an alternative to general anesthesia (GA) for hemorrhoid surgery but they all require a trained anesthetist and have numerous known complications. Since, anesthesiologists are not always available then local anesthesia is an alternative mode of anesthesia that surgeon can safely carry out by their own. Local anesthetic produce a loss of sensation and muscle paralysis in a circumscribed area of body by localized effect on peripheral nerve endings. The local anesthesia is able to provide fully relaxation of the anal canal which is an ideal setting for various anal surgical procedures. The results of hemorrhoid surgery under this mode of anesthesia have been demonstrated in many publications. Local anesthesia is a safe and effective technique while fewer risks and complications compared with general or spinal anesthesia. In Thailand both spinal anesthesia and local perianal block have routinely been used for various kinds of anorectal surgery. However, so far there has no any trial conducting to compare between these two techniques.

Detailed Description

Objectives: To study analgesic efficacy, postoperative voiding problems, patients' satisfaction, and other complications after closed hemorrhoidectomy comparison between local perianal block and spinal anesthesia.

Research design: Randomized controlled trial Setting: Phramongkutklao Hospital Research methodology: A total of 64 subjects (32 males and 32 females) underwent elective hemorrhoidectomy were randomly allocated into two groups. Thirty-two patients were randomly allocated to receive spinal anesthesia (SA group) while 32 patients received local perianal block (LA group). Duration of analgesic effect, pain measurement with visual analogue scale (VAS) at 6 and 24 hours, quantity of analgesic medication administered, postoperative complication, and patient's satisfaction with the anesthetic technique were recorded.

Study Timeline

• Study Start: 2006-12
• Study Completion: 2007-11
• Status Verified: 2009-06
• Study First Submitted: 2009-06-18
• Study First Submitted QC: 2009-06-19
• Last Update Submitted: 2009-06-19
• Study First Posted: 2009-06-22
• Last Update Posted: 2009-06-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Not specified
• Target Recruitment: 64

Inclusion Criteria

1. Patients aged between 18 and 60 years with grade 3 or 4 hemorrhoid.
2. Had no history of bupivacaine allergy.

Exclusion Criteria

1. Complicated hemorrhoid e.g. prolapsed or incarcerated hemorrhoid, gangrenous hemorrhoid.
2. Associated anorectal disease.
3. Patients whose characteristics of his/her buttock were difficult to gained adequate exposure when performing surgery under local anesthesia such as the mounds of his/her buttock is very high and rise almost straight up from the anal verge.
4. Patient was unfit for surgery e.g. heart disease, liver cirrhosis, or coagulopathy.
5. Patients who had symptoms of benign prostatic hypertrophy or bladder neck obstruction.
6. Pregnancy.
7. Patients with neuropsychotic problems.
8. Did not agree to participate this study

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
1	spinal block	spinal anesthesia: Active Comparator The SA group were received a subarachnoid block with 1.5-2.0 ml of 0.5% bupivacaine.
2	Perianal block	Perianal block with 0.25% bupivacaine

Primary Outcome Measures

Name	Time	Method
The degree of pain measured by visual analogue scale at 6 and 24 hrs after surgery.	within 24 hrs

Secondary Outcome Measures

Name	Time	Method
Patients' satisfaction with the anesthetic techniques, postoperative voiding complications, and other complications	within 24 hrs