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Usefulness of a pad soaked with pain relieving medicine for Reducing Pain and Ensuring Effectiveness of Injections to prevent Rabies following animal exposures

Effect of 2% Lignocaine Medicated Pad (LMP) Administration on Pain Relief and Antibody Response During Rabies Immunoglobulin (RIG) Infiltration: A multicentric randomized controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104578
Enrollment
600
Registered
2026-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: W540- Bitten by dog Health Condition 2: W558- Contact with other mammals

Interventions

Intervention1: 2% Lignocaine Medicated Pad: Dose 2% Lignocaine 5ml or the volume required to soak the pad and cover the wound frequency - single application twenty minutes before rabies immunoglobu

Sponsors

Indian Council of Medical Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult Patients more than 18 years coming to the Preventive Clinic or Antirabies clinic with Category three animal bites in whom Rabies Immunoglobulin Equine Rabies immunoglobulin or Human Rabies Immunoglobulin is advised. Children between 12 and 18 years with Category three animal bites in whom Rabies Immunoglobulin Equine Rabies immunoglobulin Human Rabies Immunoglobulin is advised will also be recruited after completion of six months of data collection and after the first DSMB review

Exclusion criteria

Exclusion criteria: The exclusion criteria are those who are not giving consent, known allergy to Lignocaine, history of contact dermatitis, any contraindications to lignocaine and all mucosal exposures.

Design outcomes

Primary

MeasureTime frame
Difference in Pain score in the intervention and control arm measured by Visual Analog Scale and Sound Eye Motor ScaleTimepoint: Before Rabies Immunoglobulin (RIG) administration During RIG Administration After RIG administration

Secondary

MeasureTime frame
cost-effectivenessTimepoint: one point after the procedure;adverse eventsTimepoint: till 42 days;factors determining immune responseTimepoint: one point during analysis

Countries

India

Contacts

Public ContactZinia Thajudeen Nujum

School of Public Health, Kerala University of Health Sciences

drzinia@gmail.com09037356908

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026