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Comparison the effect of intravenous analgesia by fentanyl versus ketamine in patients undergo coronary heart surgery

Clinical trial of the effect of intravenous analgesia by fentanyl compared to ketamine in patients undergo coronary heart bypass surgery

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017041233381N1
Enrollment
160
Registered
2017-05-08
Start date
2017-02-19
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Coronary artery surgery. Atherosclerotic heart disease

Interventions

Intervention 1: First group: Bolus intravenous infusion of 50 micrograms fentanyl followed by pump infusion of 5 to 50 micrograms per cc in speed in hour. Intervention 2: Second group: bolus intraveno
Treatment - Drugs
First group: Bolus intravenous infusion of 50 micrograms fentanyl followed by pump infusion of 5 to 50 micrograms per cc in speed in hour
Second group: bolus intravenous infusion of 0.5 millirograms per kilogram of ketamine followed by pump infusion of 0.5 millirograms per kilogram in hour.

Sponsors

Vice chancellor for research, Zahedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Main inclusion criteria: pre-operation ejection fraction above 30%; class one to three of ASA; no simultaneous heart valves involvement; no need of intra-aortic pump usage during the operation. Main exclusion criteria: positive history of sensitivity to study drugs; uncontrolled systemic disease such as diabetes; addiction to alcohol and drugs; positive history of psychologic disease and depression; asthma and other hypersensitivity reactions; intraoperative fracture of sternum and ribs; pre-operative liver enzymes rising higher than two folds; other chest pain causes other than coronary arteries; presence of neurologic signs and symptoms; any type of consciousness impairment pre-operation.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Postoperation pain. Timepoint: Two houres, four houres, eight houres, 12 houres and 24 houres after surgery. Method of measurement: VAS Criteria.;Mean arterial pressure. Timepoint: Up to 24 hours after surgery in intervals of every 4 hours. Method of measurement: Millimeter of mercury.;Heart rate. Timepoint: Up to 24 hours after surgery in intervals of every 4 hours. Method of measurement: Beats in minute.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarziye Yousefi

Zahedan University of Medical Sciences

Dr.yousefi@zaums.ac.ir+98 54 3329 5583

Outcome results

None listed

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