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Comparison Of Analgesic Efficacy Of Nebulized Dexmedetomidine And Lignocaine On Post-Operative Pain in tonsillectomy Under General Anaesthesia.

Comparison of analgesic efficacy of nebulized dexmedetomidine and lignocaine on post-operative pain in pediatric tonsillectomy under - CAENDL-PPT

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100240
Enrollment
74
Registered
2026-01-02
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: J039- Acute tonsillitis, unspecified

Interventions

Intervention1: DEXMEDETOMIDINE: 1. Nebulization with dexmedetomidine 2 g/kg diluted upto 4 mL with normal saline 30 minutes before induction Intervention2: Nil: Nil Control Intervention1: LIGNOCAINE:

Sponsors

BPSGMC KHANPUR KALAN SONIPAT
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Pediatric patients aged between 4 to 12 years 2.Scheduled for elective tonsillectomy under general anaesthesia. 2.ASA physical status I or II.

Exclusion criteria

Exclusion criteria: 1.Patients with any congenital abnormality 2.Patients with upper respiratory tract infection and having known allergy to dexmedetomidine, lignocaine, or any other local anaesthetics. 3.History of any neurological disorders (e.g., cerebral palsy, epilepsy). 4.Severe systemic illnesses (e.g., cardiovascular, hepatic, or renal diseases). 5.Children with a history of previous airway surgery 6.Patients and /or his/her legally acceptable representative not willing to participate in the present study. SAMPLE SIZE AND SAMPLING: As per previously conducted study

Design outcomes

Primary

MeasureTime frame
Duration of effective postperative analgesia (Time of first rescue analgesic and total analgesic doses in 24 hours) Timepoint: Every 30 minutes

Secondary

MeasureTime frame
Time to first oral intakeTimepoint: ;Emergence agitation score using PAED scaleTimepoint: followed @ 5,10,15 and 30 min post-extubation;Sedation scoreTimepoint: @ 1 and 24 hours interval;Haemodynamic parametersTimepoint: Prenebulisation,postnebulisation,@induction ,every 5 minutes intraoperatively and post operatively @30 min.,1,2,4,6,12,24 hours interval;Incidence of side effects (bradycardia,hypotension,nausea,vomiting,respiratory depression)Timepoint:

Countries

India

Contacts

Public ContactDR PRATEEK

BPS GMC KHANPUR KALAN SONIPAT

kirtiahuja2812@gmail.com9992111890

Outcome results

None listed

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