Comparison of Fentanyl and Apotel in post surgery pain management in laparascopic cholecystectomy, at Besat Hospital, 2024-2025

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20251012067596N1

Enrollment

Registered

2025-11-04

Start date

2025-11-22

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

cholecystectomy. Acquired absence of other parts of digestive tract

Interventions

Intervention 1: Control group: Patient receiving fentanyl. Intervention 2: Intervention group: Patient recieving Apotel.

Eligibility

Sex/Gender

All

Age

18 Years to 6 Years

Inclusion criteria

Inclusion criteria: All patients who are candidates for laparoscopic cholecystectomy surgery referred to Besat Hospital

Exclusion criteria

Exclusion criteria: 1. Patients under 18 years or over 60 years old2. Lack of consent to participate in the study3. Having an ASA score of three or higher4. Addiction to narcotic substances

Design outcomes

Primary

Measure	Time frame
Pain control. Timepoint: Start of study - 30 minutes after surgery. Method of measurement: VRS.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNeda Alizadeh

Hamedan University of Medical Sciences

nedaalizadeh6168@gmail.com+98 911 320 9296

Outcome results

None listed

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