Ignite Creation Date:
2024-05-06 @ 8:26 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06387095
Status:
RECRUITING
Last Update Posted:
2024-04-26
First Post:
2024-04-04
Brief Title:
Efficacy of Parasternal Blocks in Cardiovascular Surgery Patients Undergoing Median Sternotomy
Sponsor:
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
Organization:
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
Study Overview
Official Title:
Efficacy of Parasternal Blocks in Cardiovascular Surgery Patients Undergoing Median Sternotomy Randomized Controlled Study
Status:
RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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 patients 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 andor 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
Detailed Description:
The study will proceed in three arms The first group is the control group and will receive total intravenous anaesthesia as infusion after peroperative induction until the patient leaves the operating room The second group will receive ultrasound-guided parasternal superficial plan block after induction The third group will receive ultrasound-guided parasternal deep plan block Extubation times additional analgesic needs pain scores intensive care unit duration and hospital discharge times will be compared in the three groups during intensive care unit follow-up After extubation patient-controlled analgesia will be applied for 24 hours with pca infusion pump device
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None