Effect of Sacral Erector Spinae Plane Block on Hemorrhoid and Pilonidal Sinus Surgery

Not Applicable

Completed

• Conditions: Pain, Acute Post-Operative; Pilonidal Sinus; Hemorrhoids; Anesthesia
• Interventions: Procedure: sacral ESPB

• Registration Number: NCT06459739
• Lead Sponsor: Erzincan Binali Yildirim Universitesi

Brief Summary

Introduction: This study investigated the efficacy of sacral erector spinae plane block (ESPB) for managing postoperative pain and reducing opioid consumption in patients undergoing hemorrhoid and pilonidal sinus (PS) surgery.

Detailed Description

Introduction: This study investigated the efficacy of sacral erector spinae plane block (ESPB) for managing postoperative pain and reducing opioid consumption in patients undergoing hemorrhoid and pilonidal sinus (PS) surgery.

Study Timeline

• Study Start: 2023-09-01
• Primary Completion: 2024-03-01
• Study Completion: 2024-04-01
• Study First Submitted: 2024-06-05
• Study First Submitted QC: 2024-06-10
• Study First Posted: 2024-06-14
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-25
• Last Update Posted: 2025-02-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

• American Society of Anesthesiologists (ASA) I-II patients undergoing hemorrhoid and pilonidal sinus surgery

Exclusion Criteria

• patients with coagulopathies, pregnant women, patients with significant cardiovascular, hepatic, or renal disease, patients who declined spinal anesthesia or were contraindicated for it, and patients who had previously undergone the same surgery

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
sacralESPB	sacral ESPB	Sacral ESPB group

Primary Outcome Measures

Name	Time	Method
Postoperative pain	0.5,2,8,24 hours	Numeric rating scale evaluation after surgery. Use 0 to 10 points with 0 no pain 5 moderate pain and 10 severe pain.

Secondary Outcome Measures

Name	Time	Method
Opioid consumption	0.5,2,8,24 hours	Admission of tramadol as a rescue analgesia

Trial Locations

Locations (1)

Erzincan Binali Yildirim university; 🇹🇷 Erzincan, Turkey