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Regional blocks for patients undergoing thoracic surgeries-DSAPB vs RLB

Ultrasound guided Deep Serratus Anterior Plane Block vs Retrolaminar Block in patients undergoing posterolateral thoracotomy-A randomised control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/047952
Enrollment
40
Registered
2022-12-07
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: J479- Bronchiectasis, uncomplicated Health Condition 2: C349- Malignant neoplasm of unspecifiedpart of bronchus or lung Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided Deep Serratus Anterior Plane Block: The patient will be lying in a supine position with arms abducted to 90o. An ultrasound probe (L38 â?? 1-5-10MHz, Sonosite, Inc, Bo

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Patients undergoing unilateral posterolateral thoracotomy. 2) American Society of Anaesthesiologists (ASA) I or II.

Exclusion criteria

Exclusion criteria: 1)Patient with anticoagulation or bleeding disorder. 2)Pre-existing block site infection. 3)Allergy to local anaesthetics. 4)History of (H/O) daily consumption of analgesics. 5)H/O opiate abuse. 6)Previous surgery in the thoracic vertebral region. 7)Pre-existing chronic pain or cognitive dysfunction.

Design outcomes

Primary

MeasureTime frame
To assess the quality of Analgesia based on VAS pain score at rest in the postoperative period for 48 hours. Timepoint: To assess VAS at 0 1 2 3 4 5 6 9 12 15 18 24 30 36 42 48 hrs in the post operative period.

Secondary

MeasureTime frame
1)The total dose of opioids received in the postoperative period (at the first 48 hours). 2)The total dose of opioids received in the intraoperative period. 3)Time taken for the first dose of rescue analgesia. 4)Incidence of Nausea and vomiting, block complications.Timepoint: 48 hrs in the post operative period.

Countries

India

Contacts

Public ContactArun Kuttiappan

PGIMER

dr.kpgouravkalla@gmail.com8194952345

Outcome results

None listed

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