CTRI/2021/06/034296
Completed
未知
A prospective, randomized, single blinded study to compare analgesic efficacy of pectointercostal fascial block and erector spine block in patients undergoing cardiac surgery- a pilot study
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- A
- Enrollment
- 30
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Adult (more than 18 years)
- •Undergoing cardiac surgery with midline sternotomy
- •Haemodynamically stable
- •Elective surgery
- •Extubation within 3 hrs of performing block
Exclusion Criteria
- •Hemodynamic instability (left ventricular ejection fraction \<30%, on ventricular assist device)
- •Aortic surgery
- •Emergency surgery
- •Minimally invasive procedures
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Phase 4
A study comparing two brands of Bonewax for controlling bleeding from bone edges, when breast bone is cut during cardiovascular surgeriesCTRI/2022/03/041192Healthium Medtech Limited92
Recruiting
Not Applicable
A randomised, prospective, single blind study comparing a standard metal on polyethylene cemented socket in primary hip replacement versus an uncemented ceramic on ceramic bearing socket in patients under 65 years oldISRCTN53483743Record Provided by the NHSTCT Register - 2006 Update - Department of Health322
Recruiting
Phase 4
A research study to explore the occurrence of side effects of darifenacin and trospium on eye, the two drugs used in the treatment of patients with increased frequency of urination, urgency, nocturia with or without urinary leakageCTRI/2014/09/004999Dr Manjunatha R self30
Completed
Not Applicable
Comparison of Ultrasonographic method with Age-based formula for estimation of paediatric cuffed endotracheal tube size.Health Condition 1: O- Medical and SurgicalCTRI/2019/04/018755Rainbow childrens hospitals and birth right120
Recruiting
Phase 4
Prospective, randomized, single-blinded study to test the applicability of extracorporeal shock wave therapy for the treatment of temporomandibular dysfunction.K07.6Temporomandibular joint disordersDRKS00027987niversitätsmedizin der Johannes Gutenberg-Universität Mainz52