Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT07534488
NA

Sacral Erector Spinae Plane Block in Pilonidal Sinus Surgery

Sponsor: Medipol University

View on ClinicalTrials.gov

Summary

This study aims to evaluate the efficacy of ultrasound-guided Sacral Erector Spinae Plane (ESP) block for postoperative analgesia management in patients undergoing pilonidal sinus surgery under general anesthesia

Official title: Evaluation of the Efficacy of Ultrasound-Guided Sacral Erector Spinae Plane Block in Postoperative Analgesia Management in Patients Undergoing Pilonidal Sinus Surgery

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2026-04-20

Completion Date

2026-09-15

Last Updated

2026-07-27

Healthy Volunteers

No

Interventions

PROCEDURE

Sacral Erector Spinae Plane Block

Immediately after the surgical procedure and before extubation, ultrasound-guided (Vivid Q) Sacral ESPB will be applied to the patient in the prone position using a total volume of 20 ml.

DRUG

Standard Postoperative Analgesia

No block will be applied to this group. Both groups will receive intravenous 400 mg ibuprofen and 100 mg tramadol 20 minutes before the end of the surgery, and routine 1000 mg paracetamol every 8 hours postoperatively

Locations (1)

Istanbul Medipol University

Istanbul, Turkey (Türkiye)