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Use of pain reducing spray for spinal needle puncture

Use of 10% Lignocaine spray skin anaesthesia before subarachnoid blockade in patients undergoing casearean section: A prospective, randomized, double blinded placebo controlled trial. - nil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/065761
Enrollment
90
Registered
2024-04-16
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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: lignocaine 10% spray: lignocaine 10% spray will be applied 120 seconds before prick of spinal needle to patient for providing spinal anaesthesia. Control Intervention1: normal saline sp

Sponsors

Dr Annu choudhary
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients posted for elective caesarean section under subarachnoid block.

Exclusion criteria

Exclusion criteria: 1.Patient’s refusal to participate 2.Any allergy to local anesthetics 3.Coagulation disorders 4.Infection at the site of intervention 5.History of any underlying cardiac, renal dysfunction • Viral marker status positive

Design outcomes

Primary

MeasureTime frame
To compare maternal satisfaction for anaesthesia service at the end of surgery by 5 point likert scaleTimepoint: At the Post anesthesia Care Unit (0 hr)

Secondary

MeasureTime frame
1. Comparison of pain on spinal needle insertion 2. Comparison of number of pricks required for administering spinal anaesthesia 3. Investigate whether pain during puncture has an influence on choosing spinal anaesthesia again in the futureTimepoint: after injecting drug in subarachnoid space for spinal anaesthesia & at the end of surgery

Countries

India

Contacts

Public ContactAnnu Choudhary

Indira Gandhi Institute of Medical Sciences, Patna

anucdry@gmail.com07385161632

Outcome results

None listed

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