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Comparison of paracetamol and ketorolac on pain management in patients with opium abuse undergoing cardiac surgery

Comparison of the effect of paracetamol and ketorolac on pain management in patients with non-synthetic opium abuse undergoing off pump Coronary artey bypass grafting

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150216021098N5
Enrollment
100
Registered
2018-04-19
Start date
2018-04-21
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Coronary artery bypass grafting. Complications of cardiac and vascular prosthetic devices, implants and grafts

Interventions

Intervention 1: Intervention group 1: In the paracetamol group, the patients receive the drug 15 mg/kg at maximum 1 gram intravenously every 6 hours after arrival at ICU for 24 hours. Intervention 2:

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult older than 18 years undergoing off-pupm CABG ASA class 2 or 3 Non-synthetic opium abuse

Exclusion criteria

Exclusion criteria: Allergy to either of drugs Consumption of either drugs in the past 48 hours Preoperative use of nephrotoxic drugs Presence of renal insufficiency or plasma creatinine higher than 1.3 mg/dL History of gastrointestinal disease or bleeding, peptic ulcer, perioperative bleeding Hepatic insufficiency Ejection fraction less than 40% Postoperative need for intraaortic ballon pump perioperative hemodynamic compromise Unwanter intraoperative events including arrhythmia or cardiac arrest refusal to stay in the study

Design outcomes

Primary

MeasureTime frame
Pain intensity. Timepoint: every one and four hours in the first and second days, respectively after intervention. Method of measurement: Observation (CPOT0 and questioning (NRS) scores.

Secondary

MeasureTime frame
Additional analgesic requirement. Timepoint: every one hour on the first day and every 4 hours on the second day. Method of measurement: Recording the amount of administered fentanyl in micro-gram.;Frequency of acute kidney injury. Timepoint: Every day after intervention until discharge from the hospital. Method of measurement: AKIN criteria.;Frequency of gastrointestinal bleeding and discomfort. Timepoint: every day after intervention until discharge from the hospital. Method of measurement: Observation and questioning.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShahram Amini

Maragheh University of Medical Sciences

aminish@mums.ac.ir+98 51 3180 2315

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 18, 2026