Comparison of combined pectoralis plane and intercostal nerve block with local anaesthetic technique for pain relief during placement of cardiac electronic devices.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: I459- Conduction disorder, unspecified
- Registration Number
- CTRI/2021/09/036236
- Lead Sponsor
- Jawaharlal Institute of Post graduate Medical education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA 1 to 3 ,undergoing cardiac implantable electronic device implantations in the left thoracic subcutaneous location.
Exclusion Criteria
1)Patient refusal
2)Local anaesthetic allergy
3)Opioid addiction
4)Neuropsychiatric disorders
5)Infection/tumour at the site of device insertion.
6)Patients posted for reimplantation of cardiac implantable electronic devices.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare differences in intra-procedural pain scores at six time points between both groups.Timepoint: TIME POINT 1: At skin incision <br/ ><br>TIME POINT 2: At the time of venous access by cephalic vein cutdown or axillary vein puncture <br/ ><br>TIME POINT 3: During preparation of the subfascial pocket <br/ ><br>TIME POINT 4: During attachment of the leads with suture material to the pectoralis major muscle <br/ ><br>TIME POINT 5: The insertion of the device into the prepared pocket <br/ ><br>TIME POINT 6: The skin closure <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1)To compare differences in postprocedural pain scores at various time points between both groups. <br/ ><br>2)To compare the length of hospital stay <br/ ><br>3)To compare the differences in intra operative and postoperative analgesic requirements. <br/ ><br>4)To compare the complication rate in both groups.Timepoint: 1)Pain scores after 1,2,4,8 and 24 hours after the procedure.