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study to compare two ultrasound guided blocks i.e pectointercostal fascial block and erector spine block in patients undergoing cardiac surgery- a pilot study

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034296
Enrollment
30
Registered
2021-06-18
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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: pectointercostal fascial block: pectointercostal fascial block ropivacaine 0.2% 20ml on each side Control Intervention1: bilateral erector spine block: ropivacaine 0.2% 20ml on each s

Sponsors

None listed

Eligibility

Inclusion 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

Exclusion criteria: Hemodynamic instability (left ventricular ejection fraction Aortic surgery Emergency surgery Minimally invasive procedures

Design outcomes

Primary

MeasureTime frame
total opioid consumption Timepoint: 24hrs after surgery—

Secondary

MeasureTime frame
pain at rest pain on deep breathingTimepoint: 24 hrs aftersurgery—

Countries

India

Contacts

Public Contactdr manish keshwani

AIIMS, RAIPUR

drsamar0002@gmail.com8014910806

Outcome results

None listed

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