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Effect of opioid-free anesthesia and Analgesia on outcomes after pediatric dental surgery

Optimizing the Recovery of Pediatric Dental Surgery: Application of Opioid-Free Anesthesia and Analgesia: A clinical trial study in Ahvaz

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250427065484N2
Enrollment
100
Registered
2025-11-08
Start date
2025-11-21
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Post Operative Pain. Other acute postprocedural pain

Interventions

Intervention 1: Intervention group: Initial anesthesia will be initiated with 8% sevoflurane and 4L/m oxygen. After monitoring vital signs and establishing intravenous access, propofol (2–3 mg/kg) and

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 6 Years

Inclusion criteria

Inclusion criteria: 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: Developmental delay or cognitive impairment Morbid obesity Neuromuscular and craniofacial diseases Intellectual disability Emergency surgery

Design outcomes

Primary

MeasureTime frame
Post Operative Pain. Timepoint: 10, 20, and 30 minutes after surgery. Method of measurement: We used the Face, Legs, Activity, Cry, and Consol ability (FLACC) score to assess the degree of pain caused by objective pain-induced behavioral changes.

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.;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