FindTrial
Sign In

Comparing two pain releiving procedures in cardiac surgeries

Comparison of efficacy between the Erector Spinae plane block and Pecto-intercostal facial plane block in patients undergoing cardiac surgeries with midline sternotomy- A Randomised Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/051149
Enrollment
64
Registered
2023-03-28
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I259- Chronic ischemic heart disease, unspecified Health Condition 2: I248- Other forms of acute ischemic heart disease Health Condition 3: I069- Rheumatic aortic valve disease, unspecified Health Condition 4: I059- Rheumatic mitral valve disease, unspecified Health Condition 5: I089- Rheumatic multiple valve disease,unspecified

Interventions

Intervention1: NA: NA Intervention2: Not Applicable: Not applicable Intervention3: Erector spinae plane block: In our study we are going to compare the efficacy between Pecto intercostal fascial plane

Sponsors

Madras Medical Mission hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age > 18 years 2. ASA 3/4 3. Coronary artery bypass grafting surgeries 4. valve surgeries 5. combined CABG + valve surgery

Exclusion criteria

Exclusion criteria: 1. Patients not giving consent. 2. Age 3. Vascular surgeries 4. Perioperative cardiac arrest 5. Allergy to local anaesthetics. 6. Cardiogenic shock 7. Emergency surgery 8. Redo surgery 9. Preoperative Intra Aoprtic Baloon pump

Design outcomes

Primary

MeasureTime frame
Cumulative morphine useTimepoint: 24 hours post operatively—

Secondary

MeasureTime frame
1.NRS scores post extubation till 24 hours. 2.Hemodynamic stability. 3. Cumulative fentanyl usage 4. Time to extubation (after shifting the patient to ICU) 5.Time of first rescue analgesia. 6. Respiratory Rate 7. Gas parameters (Ph, Pco2, Po2, RBS, BE, Lactate 8.Complications if any. 9. Need for blood transfusions Re-explorations if any. Timepoint: 24 hours post operatively—

Countries

India

Contacts

Public ContactDr Balakrishnan N

Madras Medical Mission Hospital

balanarayanan872387@gmail.com8754515130

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026