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Comparing the use of application of a cream to reduce pain on spinal anaesthesia versus injection of pain drug.

Comparison of patient acceptability between local application of EMLA cream versus lignocaine infiltration prior to subarachnoid block in patients undergoing elective caesarean section. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062509
Enrollment
20
Registered
2024-02-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: EMLA CREAM: In Group A patients 5 X 5cm patch of EMLA cream will be applied over L 3-4 and L4-5 level of the lumbar spine on the back and covered with an occlusive dressing, about one

Sponsors

Amrita Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parturients between 18 â?? 40 years undergoing elective caesarean section under spinal anesthesia.

Exclusion criteria

Exclusion criteria: 1. History of significant cardiac, renal or liver diseases 2. Hypersensitivity to study medications 3. Anaemia (Hb less than 10) 4. Coagulation disorders 5. Patients on antiplatelets or anticoagulants 6. Local infection 7. Methhemoglobinemia

Design outcomes

Primary

MeasureTime frame
patient acceptability between local application of EMLA cream versus lignocaine infiltration prior to subarachnoid blockTimepoint: After subarachnoid block

Secondary

MeasureTime frame
assess the pain score during subarachnoid block, ease of insertion of spinal needle, adequacy of positioning, time taken, number of attempts for successful subarachnoid block, need for supplementary local infiltration, need to change position to sitting, need to attempt spinal at a different spinal interspace and the hemodynamic responses during conduct of spinal anaesthesiaTimepoint: baseline, before insertion of spinal needle, 1 minute, 5 minutes and 10minutes after spinal anesthesia

Countries

India

Contacts

Public ContactRoniya Ann Roy

Amrita institute of medical sciences cochin

sunilrajan@aims.amrita.edu09074984098

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Aug 9, 2026