Comparing Of Ketrolac Plus Apotel and Meperidine in Decrease Of Pain After surgery

Comparing Of Ketrolac Plus Apotel and Meperidine in Decrease Of Pain After Right Thoracotomy

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20210921052538N1

Enrollment

Registered

2022-06-08

Start date

2021-12-26

Completion date

Unknown

Last updated

2022-06-27

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

Conditions

surgery.

Interventions

Intervention 1: Control group: receive meperidine in case of pain ( 0.5 -1mg/kg). Intervention 2: Intervention group:Intravenous ketorolac - paracetamol:At the beginning of recovery in the interventio

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients undergoing right thoractomy

Exclusion criteria

Exclusion criteria: epidural / spinal anesthesia Patients with a history of addiction Patients with a history of coagulation disorders and platelets less than one hundred thousand. until the History of kidney failure Serum creatinine more than one and a half Patients with a history of hyperthyroidism

Design outcomes

Primary

Measure	Time frame
Blood pressure,. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Mercury sphygmomanometer.;Oxygen saturation. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Pulse oximeter.;Transpiration. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Ocular observation.;Pain level. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Pain questionnaire.	—

Measure

Time frame

Blood pressure,. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Mercury sphygmomanometer.;Oxygen saturation. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Pulse oximeter.;Transpiration. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Ocular observation.;Pain level. Timepoint: Immediately after the surgery and in the recovery room at 30 minute intervals. Method of measurement: Pain questionnaire.

—

Secondary

Measure	Time frame
Pulse. Timepoint: 30 min. Method of measurement: heart monitoring.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlireza Shariifian

Mashhad University of Medical Sciences

Salehiam1@mums.ac.ir+98 51 3604 9687

Outcome results

None listed

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