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NCT06459739 Clinical Trial

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

Anesthesia Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06459739
Other study ID # SacralESPB
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2023
Est. completion date April 1, 2024

Study information
Verified date June 2024
Source Erzi?ncan Binali Yildirim Uni?versi?tesi?
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 70
Est. completion date April 1, 2024
Est. primary completion date March 1, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Procedure:
• sacral ESPB
sacral ESPB

Locations
Country Name City State
Turkey Erzincan Binali Yildirim university Erzincan

Sponsors (1)
Lead Sponsor Collaborator
Erzi?ncan Binali Yildirim Uni?versi?tesi?

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Postoperative pain Numeric rating scale evaluation after surgery. Use 0 to 10 points with 0 no pain 5 moderate pain and 10 severe pain. 0.5,2,8,24 hours
Secondary Opioid consumption Admission of tramadol as a rescue analgesia 0.5,2,8,24 hours
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