Sacral Erector Spinae Plane Block in Pilonidal Sinus Surgery
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorMedipol University
About this trial
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
Eligibility criteria
Qualifiers
Patients scheduled for elective pilonidal sinus surgery.
ASA physical status I and II
Disqualifiers
Allergy or sensitivity to local anesthetics or opioid drugs.
Infection at the block site.
Alcohol or drug addiction.
Use of anticoagulant agents.
Trial design
Treatments tested in this trial
- Sacral Erector Spinae Plane Block
- Standard Postoperative Analgesia
Treatment groups
60 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov