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The effect of Tramadol on postoperation pain control in children undergoing Tonsillectomy and Adenotonsillectomy

Comparison of Tramadol and Placebo on postoperation pain control in children undergoing Tonsillectomy and Adenotonsillectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013082014199N3
Enrollment
72
Registered
2013-11-03
Start date
2012-07-05
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

Acute pain. Acute pain

Interventions

Intervention 1: Injection Tramadol 2 mg/kg(Manufacturer: Tehran Shimi) was diluted with Saline to 10 cc and was put on both tonsillar fossa for 5 minutes. Intervention 2: Swab soaked in10 cc of normal
Prevention
Injection Tramadol 2 mg/kg(Manufacturer: Tehran Shimi) was diluted with Saline to 10 cc and was put on both tonsillar fossa for 5 minutes
Swab soaked in10 cc of normal saline and was given on both tosillar fossa

Sponsors

Research Council of Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Children aged 4-10 years old, who were in ASA physical status classification and have been placed in groups I and II, and they were candidates for tonsillectomy with or without adenoidectomy. Exclusion criteria: Sensitivity to opioids or local anesthetics, contraindication opioids or local anesthetics, Asthma, kidney disease, liver disease, throat infections, coagulation disorders

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Acute pain. Timepoint: At 0(Recovery), 2, 4, 6, 12, 18 and 24 hours after the operation and 7 days after that. Method of measurement: wong Baker visual scale.

Secondary

MeasureTime frame
Nausea and Vomiting. Timepoint: At 0(Recovery), 2, 4, 6, 12, 18 and 24 hours after the operation and 7 days after that. Method of measurement: Observation.;Bleeding. Timepoint: At 0(Recovery), 2, 4, 6, 12, 18 and 24 hours after the operation and 7 days after that. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Mahmoudreza Alebuye

Rasoul Akram Hospital, Ear-Nose-Throat [ENT] operating room, Department of ear-Nose-Throat [ENT]

m-alebouyeh@tums.ac.ir+98 21 6435 2458

Outcome results

None listed

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