Lumbar Erector Spinae Block vs. Conventional Multimodal Analgesia for Hip Surgery Pain Management.

A Comparative study on single shot lumbar erector spinae block using 0.25% bupivacaine with conventional multimodal versus conventional multimodal analgesia alone in patients undergoing hip surgery - nil

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/060144

Enrollment

Registered

2023-11-22

Start date

Unknown

Completion date

Unknown

Last updated

2023-12-19

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

Conditions

Health Condition 1: S720- Fracture of head and neck of femur

Interventions

Intervention1: lumbar erector spinae block: lumbar erector spinae block at L4 level with 30 ml of 0.25% bupivacaine Intervention2: inf. Acetaminophen: inf. acetaminophen 1 gm iv TDS for 2 days Control

Eligibility

Inclusion criteria

Inclusion criteria: 1.ASA category I-II 2.Patients with written informed consent

Exclusion criteria

Exclusion criteria: 1.Patient’s refusal or request to leave study 2.Patients with known allergy to local anaesthetics. 3.Patients requiring combined spinal-epidural anaesthesia in operative/post operative period 4.Patients requiring general anaesthesia 5.ASA category III-V patients. 6.Patients with contra-indication for L-ESB (e.g., Bleeding diathesis, solid organ diseases, patients having psychiatric disorders or inability to give informed consent) 7.Patient with neurological disabilities. 8.Patients with history of routine opioid use.

Design outcomes

Primary

Measure	Time frame
To assess the quality of post operative analgesia provided by Lumbar Erector Spinae Block using 0.25% bupivacaine in cases of hip surgery measured by NRS.Timepoint: pain score checked at 0 hours, 3 hours, 6 hours, 12 hours and 24 hours	—

Secondary

Measure	Time frame
To ascertain total analgesic drugs consumptionTimepoint: 24 hours;To assess any complications arising out of either EPS block or any other complications during the course of the studyTimepoint: 24 hours;To assess patient satisfaction with the anaesthetic technique using an 11-point patient satisfaction surveyTimepoint: 24 hours;To assess the time for first rescue analgesic drugsTimepoint: 24 hours	—

Measure

Time frame

To ascertain total analgesic drugs consumptionTimepoint: 24 hours;To assess any complications arising out of either EPS block or any other complications during the course of the studyTimepoint: 24 hours;To assess patient satisfaction with the anaesthetic technique using an 11-point patient satisfaction surveyTimepoint: 24 hours;To assess the time for first rescue analgesic drugsTimepoint: 24 hours

—

Countries

India

Contacts

Public ContactDr Atasi Das

ESI-PGIMSR & ESIC MEDICAL COLLEGE, JOKA, KOLKATA

doc.atasi@gmail.com9153011075

Outcome results

None listed

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