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Comparison the effect of topical ketamine,morphine and lidocaine spray on post operative pain in tonsillectomy

Comparison the effect of topical ketamine,morphine and lidocaine spray on post operative pain in tonsillectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201104236256N1
Enrollment
124
Registered
2011-06-18
Start date
2010-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Hypertrophy of tonsils. Hypertrophy of tonsils

Interventions

Intervention 1: Intervention:lidocain spray 10%(100mg/ml) with dose 2mg/kg. Intervention 2: Control : normal saline spray. Intervention 3: Intervention:ketamine spray 1%(10mg/ml)with dose 0.5mg/kg. In
Prevention
Intervention:lidocain spray 10%(100mg/ml) with dose 2mg/kg
Control : normal saline spray
Intervention:ketamine spray 1%(10mg/ml)with dose 0.5mg/kg
Intervention:morphin spray 0.1%(1mg/ml)with dose 0.05% mg/kg

Sponsors

Vice chancellor for research, Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: Inclusion: Elective tonsillectomy surgery; age between 3-12 years; did not use anti convulsive, antiinflamatory or analgesic agents; negative history of hypersensitive reactions to morphine or lidocaine or hyperactive airway disease such asthma and testimonial form patients Exclusion : using anti convulsive, antiinflamatory or analgesic agents; history of hypersensitive reactions to morphine or lidocaine or hyperactive airway disease such asthma

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: During 20 Min. Method of measurement: FLACC (the face, legs, activity, cry and consolability).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sevak Hatamian

Qazvin University of Medical Sciences

sehatamian@qums.ac.ir+98 28 1222 2452

Outcome results

None listed

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