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Preemptive Analgesia for Postoperative Pain Control for Dental Treatment Under General Anesthesia

A

Aydin Adnan Menderes University

Status

Completed

Conditions

Pain, Postoperative

Treatments

Drug: Control
Drug: Preemptive Analgesics

Study type

Observational

Funder types

Other

Identifiers

NCT03852602
2019-18

Details and patient eligibility

About

The aim of this study was to compare the analgesic-treated children with analgesic prior to the treatment and to compare the postoperative analgesic needs of children undergoing dental treatment under general anesthesia.

Full description

The investigator's study included patients who were admitted to Inonu University and Adnan Menderes University, Faculty of Dentistry, Department of Pediatric Dentistry in 2019 and decided to perform dental treatment under general anesthesia. Patients 1 to 7 years of age with dental treatment between February 28 and June 1, 2019 will be included.

Patients who underwent analgesic 15 minutes after the induction of general anesthesia from the patients, and those who made painkillers 15 minutes before the end of the treatment will constitute the control group. Paracetamol 15 mg / kg IV will be given in 50 ml of saline.

The demographic data of the children to be included in the study such as age, gender, type of dental intervention, duration of operation, postoperative pain scores, recovery times will be recorded and compared.

Enrollment

70 patients

Sex

All

Ages

3 to 7 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • To be treated under general anesthesia
  • No systemic disease
  • To have at least one painful dental procedure in the upper and lower jaw (pulpectomy, pulpotomy

Exclusion criteria

  • Patients with mental or physical disabilities of any disease
  • Patients who have not undergone painful dental intervention under general anesthesia

Trial design

70 participants in 2 patient groups

Group Control
Description:
Analgesic application15 minutes before the end of the treatment will constitute the control group.
Treatment:
Drug: Control
Group preemptive
Description:
Patients who underwent analgesic 15 minutes after the induction of general anesthesia .
Treatment:
Drug: Preemptive Analgesics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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