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Comparison of analgesic efficacy of topical lignocaine-prilocaine cream with local infiltration of 2% lignocaine prior to spinal anaesthesia.

Comparative evaluation of analgesic efficacy of topical EMLA cream with local infiltration of 2% lignocaine prior to subarachnoid block.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/08/044614
Enrollment
60
Registered
2022-08-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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: Topical application of Eutectic Mixture of Local Anaesthetics (EMLA) cream: This group will include 30 patients in whom 2.5 gms of 5% EMLA cream per 10sq.cm will be applied for a minimu

Sponsors

Pandit BD Sharma PGIMS Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of the age 18-60 years, of either sex belonging to ASA grade I and grade II undergoing 1. elective lower abdominal surgery 2. pelvic surgery 3.lower limb surgeries will be selected

Exclusion criteria

Exclusion criteria: Following patients will be excluded 1.Patients allergic EMLA cream or any other local anaesthetics. 2. Pregnant and lactating females. 3. Patients with methaemoglobinaemia 4. Psychiatric disorders 5. Fractures 6. More than 3 attempts at lumbar puncture

Design outcomes

Primary

MeasureTime frame
•Primary objective - To compare the VAS score and 4-point pain score of topical EMLA cream with Lignocaine infiltration during subarachnoid block.Timepoint: 1.VAS Score will be assessed immediately (within 5 minutes) after lumbar subarachnoid block on the scale of 0-10. 2.the 4-point pain scale will be assessed at the time of spinal needle insertion as: 0 – no response 1 - mild facial grimace 2 - verbal response 3 - movement of the back

Secondary

MeasureTime frame
Secondary objective - 1. Haemodynamic response to pain, 2. patients’ satisfaction with analgesia technique, 3. side effectsTimepoint: 1. Haemodynamic response will be measured immediately (within 2 minutes) before and after(within 2minutes) the lumbar subarachnoid block. 2. Patients satisfaction will be assessed immediatey after lumbar subarachnoid block, within 5 minutes before the start of surgery. 3.Patient will be follow up upto 24 hours for any side effects

Countries

India

Contacts

Public ContactTeyiesito Yano

Pandit BD Sharma PGIMS, Rohtak

teyie.yano@gmail.com9774921342

Outcome results

None listed

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