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

Pain, Postoperative Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03852602
• Other study ID #: 2019-18
• Status: Completed
• Start date: February 28, 2019
• Est. completion date: March 30, 2020

Study information

• Verified date: June 2021
• Source: Aydin Adnan Menderes University
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: March 30, 2020
• Est. primary completion date: February 15, 2020
• Gender: All
• Age group: 3 Years to 7 Years

Eligibility

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

Related Conditions & MeSH terms

• Pain, Postoperative

Intervention

Drug:
• Preemptive Analgesics
Analgesic application15 minutes before the treatment
• Control
Analgesic application15 minutes before the end of the treatment

Locations

Country	Name	City	State
Turkey	Sultan KELES	Aydin

Sponsors (2)

Lead Sponsor	Collaborator
Aydin Adnan Menderes University	Inonu University

Country where clinical trial is conducted

Turkey, 

References & Publications (1)

Kharouba J, Hawash N, Peretz B, Blumer S, Srour Y, Nassar M, Sabbah M, Safadi A, Khorev A, Somri M. Effect of intravenous paracetamol as pre-emptive compared to preventive analgesia in a pediatric dental setting: a prospective randomized study. Int J Paediatr Dent. 2018 Jan;28(1):83-91. doi: 10.1111/ipd.12311. Epub 2017 Jun 15. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Postoperative dental pain	Wong-Baker faces Scale is validated for children aged 3 to 7 years, includes six cartoon faces corresponding to scores 0-5 (0=no hurt, 1= hurts a little bit, 2= hurts a little more, 3=hurts even more, 4= hurts a whole lot, 5=hurts worst).	An average of 24 hours postoperatively