NCT06387095

Efficacy of Parasternal Blocks in Cardiovascular Surgery Patients Undergoing Median Sternotomy

Efficacy of Parasternal Blocks in Cardiovascular Surgery Patients Undergoing Median Sternotomy: Randomized, Controlled Study
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital·ClinicalTrials.gov·procedureRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Postoperative Pain
Drug/Device/Intervention
1. no block
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
Location
Istanbul, Turkey
Timeline & enrollment
Phase
N/A
Start date
Feb 01, 2024
End date
Aug 01, 2025
Enrollment
300 participants
Primary outcome

postoperative chronic pain

Summary

Acute and chronic pain after cardiac surgery is a common problem that negatively affects
 quality of life. Postoperative pain after cardiac surgery is most intense in the first two
 days and decreases in the following period. However, postoperative pain with incomplete
 management in the acute period may become chronic. This may negatively affect the patient's
 quality of life. Although central blocks such as thoracic epidural and paravertebral blocks
 are considered the gold standard in analgesia control, the advantages of thoracic plan
 blocks, which are more superficial due to peroperative heparinisation; coagulation disorders;
 and procedural difficulties, are undeniable. Thoracic plane blocks, which can also be used in
 patients receiving anticoagulant and/or antiplatelet therapy, have recently been used for
 acute pain. The aim of this study was to evaluate the effect of thoracic plane blocks on
 extubation time, pain scores, intensive care unit (ICU) and hospital stays in patients
 undergoing median sternotomy.

ICD-10 classifications
Acute painPostoperative intestinal obstructionPain, unspecifiedDuring surgical operationDuring surgical operation
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06387095
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06387095 through Pure Global AI's free database. This phase not specified trial is sponsored by Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital and is currently Recruiting. The study focuses on Postoperative Pain. Target enrollment is 300 participants.

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