Comparison of Pethidine and Apotel in post surgery pain control in LAPARASCOPIC cholecystectomy, at Besat Hospital, 2024-2025

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20251012067596N2

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 specified parts of digestive tract

Interventions

Intervention 1: Control group: Petidine recieving group. Intervention 2: Intervention group: Apotel recieving group.

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: All patient who are candidates for laparoscopic cholecystetectomy surgery reffered to Besat hospitalv

Exclusion criteria

Exclusion criteria: 1. pateints under 18 yeasr or over 60 yeasr old 2. lack of consent to participate to study 3. Having an SAS score of three or higher 4. Addiction to narcotic substance

Design outcomes

Primary

Measure	Time frame
Effective pain relif with fewer side effects. Timepoint: start of ths study , 30 minute after surgery. Method of measurement: VRS scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNeda Alizadeh

Hamedan University of Medical Sciences

nedalaizdeh6168@gmail.com+98 911 320 9296

Outcome results

None listed

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