Status:
NOT_YET_RECRUITING
Comparison of PSB and RIFPB Combination With PSB and ESPB Combination in Cardiac Surgery With Sternotomy
Lead Sponsor:
Cumhuriyet University
Conditions:
Post Operative Pain
Eligibility:
All Genders
18-85 years
Phase:
NA
Brief Summary
The goal of this study is to compare the analgesic efficacy of the combination of PSB and RIFPB and the combination of PSB and ESPB in patients undergoing cardiac surgery with sternotomy.
Detailed Description
This study will consist of two randomized groups: Group RIFPB (n=12), Group ESP (n=12). All patients will receive standard general anesthesia. Group RIFPB patients will receive PSB and RIFPB with 0.25...
Eligibility Criteria
Inclusion
- Adult patients over 18 years of age who will undergo cardiac surgery with sternotomy under general anesthesia and who are in classes I-IIIII according to the American Society of Anesthesiologists (ASA) risk classification.
Exclusion
- Patients who did not give consent,
- patients with coagulopathy,
- patients with signs of infection at the block application site,
- patients using anticoagulants,
- patients with local anesthetic drug allergies,
- patients with unstable hemodynamics,
- patients who could not cooperate during postoperative pain assessment
Key Trial Info
Start Date :
August 15 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
September 20 2024
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT06553573
Start Date
August 15 2024
End Date
September 20 2024
Last Update
August 14 2024
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