Evaluating the Impact of Enhanced Recovery After Surgery (ERAS )Protocol on Analgesic Consumption in Orthognathic Surgery

Evaluating the Impact of Enhanced Recovery After Surgery (ERAS) Protocol with Maxillary and Mandibullar Trigeminal Nerve Blocks under Ultrasound Guidance on Analgesic Narcotic Consumption in Orthognathic Surgery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20120430009593N16

Enrollment

Registered

2024-07-21

Start date

2024-07-22

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

Orthognathic surgery. Congenital malformation of face and neck, unspecified

Interventions

Intervention 1: Intervention Group:Patients in this group will undergo general anesthesia with the implementation of an Enhanced Recovery After Surgery (ERAS) protocol and an ultrasound-guided trigemi

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients Candidates for Orthognathic Surgery under General Anesthesia Primary deformity ASA Class I, II Filling out the Patient's Informed Consent Form

Exclusion criteria

Exclusion criteria: History of Opioid Usage History of Post -Operative Nausea and Vomiting

Design outcomes

Primary

Measure	Time frame
Remifentanil Consumption During Operation. Timepoint: Every 1 hour During Operation. Method of measurement: Remifentan Infusion Dosage Based on Microgram.;Postoperative Analgesic consumption. Timepoint: 2 ,6,12,24 hours post operation. Method of measurement: Dosage of medications in miligram or gram.	—

Secondary

Measure	Time frame
Propofol Consumption During Operation. Timepoint: Every 1 hour during operation. Method of measurement: Propofol Consumption Based on Milligram per Hour.;Post-Op Visual Analogue Scale. Timepoint: Recovery and at 2, 4, 6, 12 and 24 hours. Method of measurement: Visual Analogue scale based on 0 to 10.;Incidence of Post -Operative Nausea and vomiting in 24 hrs. Timepoint: 2, 4, 6, 12 , 24 hours. Method of measurement: Patient expression.;Postop satisfaction score. Timepoint: before patient discharge. Method of measurement: scoring 1 to 5.	—

Measure

Time frame

Propofol Consumption During Operation. Timepoint: Every 1 hour during operation. Method of measurement: Propofol Consumption Based on Milligram per Hour.;Post-Op Visual Analogue Scale. Timepoint: Recovery and at 2, 4, 6, 12 and 24 hours. Method of measurement: Visual Analogue scale based on 0 to 10.;Incidence of Post -Operative Nausea and vomiting in 24 hrs. Timepoint: 2, 4, 6, 12 , 24 hours. Method of measurement: Patient expression.;Postop satisfaction score. Timepoint: before patient discharge. Method of measurement: scoring 1 to 5.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Memary

Shahid Beheshti University of Medical Sciences

drmemary@gmail.com+98 21 7743 7580

Outcome results

None listed

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