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effect of opioid-free anesthesia on outcomes after pediatric dental surgery

effect of opioid-free anesthesia on outcomes after pediatric dental surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250427065484N1
Enrollment
102
Registered
2025-05-15
Start date
2025-06-10
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post Operative Pain.

Interventions

Intervention 1: Intervention group: After ensuring that the patients are NPO, anesthesia induction will be performed in the intervention group with sodium thiopental 5 mg/kg body weight, atracurium 0.

Sponsors

Boushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 6 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are candidates for dental surgery aged 4 to 6 years Patients who require planned general anesthesia for elective surgery Have a physical status of ASA I and II No developmental disability or any developmental delay No psychiatric disorders and no attention deficit hyperactivity disorder Informed consent has been obtained from parents or legal guardians

Exclusion criteria

Exclusion criteria: 1. Having a drug allergy to ketorolac Having a kidney or bleeding problem History of using narcotics or sedatives in the past month Any emergency conditions encountered during surgery

Design outcomes

Primary

MeasureTime frame
Post Operative Pain. Timepoint: During extubation, 10, 20, and 30 minutes after surgery. Method of measurement: Score from the Vang Baker Visual Scale.

Secondary

MeasureTime frame
Hemodynamic parameters. Timepoint: Before induction, during induction, immediately after surgery, 10, 20 and 30 minutes after surgery. Method of measurement: Blood pressure and heart rate monitoring.;Depth of anesthesia. Timepoint: During anesthesia. Method of measurement: BIS Monitoring.;Postoperative nausea and vomiting. Timepoint: During extubation, 10, 20, and 30 minutes after surgery. Method of measurement: Observe the frequency of vomiting.;Length of stay in recovery. Timepoint: From the moment you enter to exit recovery. Method of measurement: The passage of time has passed.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Arianmehr

Ahvaz University of Medical Sciences

dr.saraArianMehr@gmail.com+98 61 3322 1023

Outcome results

None listed

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