Skip to content

A Comparative Study of Nerve block in Rhomboid Intercostal Plane and Pectoralis Plane in Patients Undergoing Cardiac Device Implantation: A Randomised Control trial

A Comparative Study of Rhomboid Intercostal Plane Block and Pectoralis Plane Block in Patients Undergoing Cardiac Device Implantation: A Randomised Control trial - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/04/109095
Enrollment
58
Registered
2026-04-22
Start date
Unknown
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Rhomboid intercostal plane block (RIB) group: Dose : 20 ml 0f 0.25% bupivacaine Route of administration : Rhomboid major intercostal plane peripheral nerve block frequency : once prior

Sponsors

AIIMS Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients belonging to ASA physical status 1-3 in the age group of 18 to 75 years, scheduled for cardiac device implantation will be enrolled in the study.

Exclusion criteria

Exclusion criteria: Refusal to participation, known allergy to local anaesthetics, psychiatric disorders, or any infection or tumour at the procedural site, bleeding disorder or coagulopathy, hepatic or renal dysfunction, CNS dysfunction, malignancy, severe systemic disease or any other condition that would be deemed a contraindication by the treating physicians.

Design outcomes

Primary

MeasureTime frame
To compare the rhomboid intercostal plane block and pectoralis plane block in patients undergoing cardiac device implantation using pain scale.Timepoint: Baseline, during procedure, postprocedure 1hour, 2 hour, 4 hour, 6 hour, 8 hour and 24 hour

Secondary

MeasureTime frame
To compare satisfaction levels of patients & doctors between the two groups.Timepoint: Post-procedure (at the end of procedure);To compare requirement of rescue analgesia between the two groups.Timepoint: Baseline, during procedure, postprocedure 1hour, 2 hour, 4 hour, 6 hour, 8 hour & 24 hour;To compare post-procedural complications between the two groups.Timepoint: till hospital stay;To compare the duration of hospital stay between the two groups.Timepoint: till discharge from hospital

Countries

India

Contacts

Public ContactT Hemanthkumar

AIIMS Delhi

abi.hemanthkumar@gmail.com9811139019

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Sep 19, 2026