FindTrial
Sign In

Peri-operative analgesic efficacy of ultrasound - guided bilateral erector spinae block spinae plane[ESP] block for adult patients undergoing lumbar spine surgeries.

Peri-operative analgesic efficacy of ultrasound - bilateral erector spinae plane [ESP] block for adult patients undergoing lumbar spine surgeries - A randomised double blind controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/09/045972
Enrollment
80
Registered
2022-09-28
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: Ultrasound Guided Bilateral Erector Spinae Plane Block: The ESP block will be performed by an experienced anaesthesiologist after induction of general anaesthesia with patients in prone

Sponsors

JSSAHER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Age - 18 to 60 years 2.ASA PHYSICAL STATUS l & ll 3.Body Mass Index 18.5 - 30 kg/ m2 4.Weight > 50 kg 5.Duration of surgery

Exclusion criteria

Exclusion criteria: Patient refusal Patient with history of allergy or contraindication to study drugs History of bleeding and coagulation disorders History of severe heart,liver,kidney,haematological disorders

Design outcomes

Primary

MeasureTime frame
To determine analgesic efficacy of ultrasound guided erector spinae block in patients undergoing lumbar spine surgeries in terms of total tramadol requirement during first 24 hour post operatively.Timepoint: to determine the analgesic efficacy of erector spinae block by assessing the Visual Analogue Score at rest and with movement during the a) Immediate post op period b) 2nd hour post op period c) 4th hour post op period d) 6th hour post op period e) 12th hour post op period f) 24th hour post op period—

Secondary

MeasureTime frame
To determine intraoperative Fentanyl and Vecuronium requirementTimepoint: during the intra-operative period;To determine rescue analgesics requirementTimepoint: post-operatively;To observe for any adverse effects of Erector Spinae Block like local hematomas infection and local anaesthetic systemic toxicityTimepoint: intraoperative and post operative period—

Countries

India

Contacts

Public ContactDr Surya Prakash Saladi

JSSAHER

dranilkumarmr@gmail.com9945155844

Outcome results

None listed

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