Comparación de los efectos de Apotel y Ketorolac antes de la cirugía sobre el dolor y la cantidad de narcóticos necesarios después de la cirugía abdominal

Comparison of the effect of Apotel and Ketorolac before surgery on pain and the need for narcotics after abdominal surgery during the first 24 hours after surgery.

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230911059408N1

Enrollment

128

Registered

2023-10-13

Start date

2023-10-22

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Pain after abdominal surgery. Unspecified complication of procedure

Interventions

Intervention 1: Intervention group: One hour before the operation, one group receives 1 gram of Apotel intravenously. Intervention 2: Control group: One hour before the operation, one group receives a

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Elective surgery ASA1,2 (American Society of Anesthesiologists) Age 18-65 years Signing a personal consent form to enter the study No abuse of drugs, alcohol, cigarettes and psychotropic drugs

Exclusion criteria

Exclusion criteria: Loss of consciousness Hemodynamic disorder Abnormal intraoperative bleeding The length of the operation more than 4 hours

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: 1, 6, 12, 24 hours after the operation. Method of measurement: Visual Analogue Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahnaz Narimani Zamanabadi

Islamic Azad University

mahnaznarimani@gmail.com+98 21 2660 2642

Outcome results

None listed

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