Erector Spinae Plane Block, Cardiac Surgery
Conditions
Brief summary
The purpose of this study is to assess efficacy of erector spinae plane block (ESP) for postoperative pain management in cardiac surgery patients.
Detailed description
After being informed about the study and potential risks, all patients giving written informed consent will be randomised (single blind) as block group(patients is performed esp block) and control group. All patients will be evaluate during 48 hours for postoperative pain.
Interventions
PROCEDUREerector spinae plane block
ESP Block: Bilateral ESP block and with ultrasound guidance will be applied A total 40 ml, 20 ml bupivacaine 0.5%, 20 ml saline.
DRUGiv analgesia
iv contromal
Sponsors
Aydin Adnan Menderes University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Must be ASA score I-III * Must be 18-75 years old * must undergo cardiac surgery
Exclusion criteria
* emergency surgery, * bleeding diathesis, * presence of contraindications to LA agents used in this study, * use of chronic opioids, * psychiatric disorders. * prolonged extubation * presence of infection at the injection site. * cardiovascular conditions (EF\<40, LMCA obstruction)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| change from baseline in pain the 10 point Visual Analog Scale (VAS) at hours 3,6,9,12,24,36,48. | baseline and hours 3-6-12-24-36-48 | The VAS is validated instrument assessing average pain. Possible scores range from 0 (no pain) to 10 (worst possible pain) Change= (hours 3,6,9,12,24,48 score- baseline) |
| time to mobilize the patient | Any time for 7 days | time to mobilize the patient is reported as when the patient is mobilized |
Countries
Turkey (Türkiye)
Contacts
Primary ContactSinem Sari, Assoc Prof
Outcome results
None listed