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Comparison of the effect of fentanyl and remifentanil alone versus the effect of adding propofol to fentanyl and remifentanil on postoperative pain intensity in patients who are candidates for cosmetic abdominal surgery

Comparison of the effect of fentanyl and remifentanil alone versus the effect of adding propofol to fentanyl and remifentanil on postoperative pain intensity in patients who are candidates for cosmetic abdominal surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241027063515N1
Enrollment
36
Registered
2024-12-08
Start date
2024-11-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Pain. Acute pain

Interventions

Intervention 1: Intervention group: The first group: 1 cc of fentanyl per hour and 2 mg of remifentanil infusion. Intervention 2: The second group: 1 cc of fentanyl per hour and remifentanil at the ra

Sponsors

Islamic Azad University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Electiveness of action No use of drugs and alcohol Sign the informed consent form to enter the study

Exclusion criteria

Exclusion criteria: The duration of the operation is more than 4 hours Abnormal intraoperative bleeding

Design outcomes

Primary

MeasureTime frame
Pain after surgery. Timepoint: in recovery and at 6, 12 and 24 hours after the operation. Method of measurement: VAS Scale.—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGhazaleh Ghasemi

Islamic Azad University

ailarghasemi98@yahoo.com+98 21 2660 2642

Outcome results

None listed

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