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Comparison of combined pectoralis plane and intercostal nerve block with local anaesthetic technique for pain relief during placement of cardiac electronic devices.

Comparison of combined pectoralis plane block and intercostal nerve block with local infiltration analgesia in patients undergoing Cardiac implantable electronic device (CIED) implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036236
Enrollment
70
Registered
2021-09-03
Start date
Unknown
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Health Condition 1: I459- Conduction disorder, unspecified

Interventions

Intervention1: PECS 1 and Intercostal nerve block: Patients in intervention arm will receive intercostal nerve block at the level of first and second intercostal spaces with 4ml of 0.375% ropivacaine

Sponsors

Jawaharlal Institute of Post graduate Medical education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1 to 3 ,undergoing cardiac implantable electronic device implantations in the left thoracic subcutaneous location.

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
To compare differences in intra-procedural pain scores at six time points between both groups.Timepoint: TIME POINT 1: At skin incision TIME POINT 2: At the time of venous access by cephalic vein cutdown or axillary vein puncture TIME POINT 3: During preparation of the subfascial pocket TIME POINT 4: During attachment of the leads with suture material to the pectoralis major muscle TIME POINT 5: The insertion of the device into the prepared pocket TIME POINT 6: The skin closure—

Secondary

MeasureTime frame
1)To compare differences in postprocedural pain scores at various time points between both groups. 2)To compare the length of hospital stay 3)To compare the differences in intra operative and postoperative analgesic requirements. 4)To compare the complication rate in both groups.Timepoint: 1)Pain scores after 1,2,4,8 and 24 hours after the procedure.—

Countries

India

Contacts

Public ContactDrSatyen Parida

Jawaharlal Institute of Postgraduate Medical Education and Research puducherry

jipmersatyen@gmail.com7708746042

Outcome results

None listed

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