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The effect of bupivacaine with lidocain and epinephrine composition on the pain in patients undergoing tonsillectomy surgery

Comparative effect of local injection of bupivacaine with lidocain and epinephrine composition on post tonsillectomy pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016072529065N1
Enrollment
87
Registered
2017-06-08
Start date
2016-11-21
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

Tonsilectomy. Chronic diseases of tonsils and adenoids

Interventions

Intervention 1: Intervention group: After induction of anesthesia, cold knife tonsillectomy will be performed. 5 minutes before the surgical incision, in the first group 2 mL of 0.125 bupivacaine, in
Treatment - Drugs
Intervention group: After induction of anesthesia, cold knife tonsillectomy will be performed. 5 minutes before the surgical incision, in the first group 2 mL of 0.125 bupivacaine, in the second group
Control group: After induction of anesthesia, cold knife tonsillectomy will be performed. There is no intervention in Group 3. The duration of anesthesia and surgery asses, also patients' Vital Signs

Sponsors

Vice chancellor for research of Yasuj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patient candidate for elective tonsillectomy; children aged 4 to 10 years; consent of the parents; lack of co-morbidities; negative history of surgery; The ability to verbal communication; cognitive and Mental health. Exclusion criteria: metabolic and endocrine diseases; coagulation disorders; mental retardation; positive history of allergy to drugs; pre-tonsilar abscess; hypertension; psychotic disorder; chronic pain; want to withdraw the study; creates complications in patients like bleeding, Late recovery (2 hours post operation); receiving narcotic drug during study; obesity

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 2,4,6 post operation surgery. Method of measurement: wong- baker scale.

Secondary

MeasureTime frame
Vital Signs. Timepoint: 2,4,6 Post Operation Surgery. Method of measurement: Sphygmomanometer,Thermometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahin Roozitalab

Yasuj University of Medical Sciences, Yasuj, Iran

mohammadi.b1391@yahoo.com? roozitalab95@gmail.com+98 74 3323 5142

Outcome results

None listed

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