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

NCT ID: NCT03852602

Last Updated: 2021-06-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

70 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-02-28

Study Completion Date

2020-03-30

Brief Summary

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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.

Detailed Description

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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.

Conditions

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Pain, Postoperative

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Group Control

Analgesic application15 minutes before the end of the treatment will constitute the control group.

Control

Intervention Type DRUG

Analgesic application15 minutes before the end of the treatment

Group preemptive

Patients who underwent analgesic 15 minutes after the induction of general anesthesia .

Preemptive Analgesics

Intervention Type DRUG

Analgesic application15 minutes before the treatment

Interventions

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Preemptive Analgesics

Analgesic application15 minutes before the treatment

Intervention Type DRUG

Control

Analgesic application15 minutes before the end of the treatment

Intervention Type DRUG

Other Intervention Names

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Preventive analgesic

Eligibility Criteria

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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
Minimum Eligible Age

3 Years

Maximum Eligible Age

7 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Inonu University

OTHER

Sponsor Role collaborator

Aydin Adnan Menderes University

OTHER

Sponsor Role lead

Responsible Party

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Sultan KELES

Assist. Prof.Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Sultan Keles, Dr.

Role: STUDY_CHAIR

Aydin Adnan Menderes University

Locations

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Sultan KELES

Aydin, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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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.

Reference Type BACKGROUND
PMID: 28618198 (View on PubMed)

Other Identifiers

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2019-18

Identifier Type: -

Identifier Source: org_study_id

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