Recruitment

Recruitment Status
Active, not recruiting

Summary

Conditions
  • Analgesia
  • Postoperative Pain
Type
Interventional
Phase
Not Applicable
Design
Allocation: RandomizedIntervention Model: Crossover AssignmentMasking: Single (Participant)Primary Purpose: Diagnostic

Participation Requirements

Age
Between 18 years and 70 years
Gender
Only males

Description

After being informed about the study and potential risks, written consent was obtained from all patients. Patients who meet eligibility requirements will be randomized in a 1:1 ratio to bi- level erector spinae plane block and modified pectoral block.

After being informed about the study and potential risks, written consent was obtained from all patients. Patients who meet eligibility requirements will be randomized in a 1:1 ratio to bi- level erector spinae plane block and modified pectoral block.

Tracking Information

NCT #
NCT04689581
Collaborators
Not Provided
Investigators
Principal Investigator: Sevim Cesur, MD Kocaeli University