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Comparision of Erector Spinae block and Fentanyl PCA in lumbar spine surgeries.

Comparison of bilateral ultrasound guided low thoracic erector spinae block and intravenous patient controlled fentanyl infusion for post-operative analgesia in lumbar surgeries ââ?¬â?? a randomised control trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030754
Enrollment
60
Registered
2021-01-27
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: M498- Spondylopathy in diseases classified elsewhere

Interventions

Intervention1: Erector Spinae Block in one of the group.: Under all aseptic precautions, the blocks will be performedin prone position after induction of anesthesia .Standard 7 Mhzlinear ultrasound tr
thereafter, the local anaesthetic (20 ml of 0.375% Ropivacaine and 2 mg dexamethasone) will be administered into the space.The same will be repeated on the opposite side. Control Intervention1: Erecto
thereafter, the local anaesthetic (20 ml of 0.375% Ropivacaine and 2 mg dexamethasone) will be administered into the space.The same will be repeated

Sponsors

Department of Anaesthesia
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing Lumbar spine surgeries.

Exclusion criteria

Exclusion criteria: 1. No consent from the patientââ?¬•s care-giver/ patients or attendant refusal. 2. Patients having history coronary artery disease, documented clinical or echo cardiac evidence of left ventricular dysfunction. 3. History of cognitive dysfunction / delirium. 4. History of Opioid use. 5. History of anticoagulation or any bleeding disorder.

Design outcomes

Primary

MeasureTime frame
1. Difference of total dose of fentanyl used in first 24 hours of post-operative period in the 2 groups.Timepoint: 1, 2, 4, 8, 12, 18 & 24 hours—

Secondary

MeasureTime frame
Adverse effects of opioids: a. Nausea vomiting b. Ileus c. Pruritis d. Drowsiness Timepoint: 1, 2, 4, 8, 12, 18 & 24 hours;Block related complications a. Hypotension b. Local anaesthesia toxicity/allergy c. Vascular puncture d. Infection e. Pleural puncture / Pneumothorax f. Failed block Timepoint: 1, 2, 4, 8, 12, 18 & 24 hours;Difference in pain score(VAS)Timepoint: 1, 2, 4, 8, 12, 18 & 24 hours;Length of hospital stayTimepoint: 1, 2, 4, 8, 12, 18 & 24 hours;Time for ambulationTimepoint: 1, 2, 4, 8, 12, 18 & 24 hours—

Countries

India

Contacts

Public ContactDr Deepak Rajappa

Sakra World Hospital

drdeepak.r4@gmail.com8437374321

Outcome results

None listed

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