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Comparing effects of morphine and ketamine on pain relief

Comparing effects of low dose injectable morphine and ketamine in patients with long bone fracture pain

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017041221480N6
Enrollment
156
Registered
2017-07-26
Start date
2017-04-21
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

Pain. Other soft tissue disorders, not elsewhere classified

Interventions

Intervention 1: Intervention group: Ketamine, 0.5mg / kg intravenous injection (by Abidi Pharmaceutical Company, Iran), one dose, zero minute of the study. Intervention 2: Intervention group: Morphine
Treatment - Drugs
Intervention group: Ketamine, 0.5mg / kg intravenous injection (by Abidi Pharmaceutical Company, Iran), one dose, zero minute of the study
Intervention group: Morphine, 1.0mg / kg slow injection (by Abidi Pharmaceutical Company, Iran), one dose, zero minute of the study

Sponsors

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

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Fracture of long bones in upper or lower extremities caused by blunt and direct trauma referring to the emergency ward; needing inject-able sedative Exclusion criteria: History of psychiatric, liver and kidney diseases, stroke, asthma and other cardiac and respiratory diseases; weight of below 45 or above 155 kg; pregnant or breastfeeding women; pressure of above 18 or below 90 mm Hg; heart rate of below 50 or above 150 per minute; respiration rate of below 10 or above 30 per minute; reduced consciousness; blow to the head or eyes; multiple trauma; allergy to the sedatives used in the research; drug addiction; use of inject-able drugs; fracture in the parts other than long bones; fracture with dislocation or fracture with extreme displacement that requires a reduction ; open fracture; compartment syndrome; lack of tendency to participate in the project; receiving sedatives before the research

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Start the intervention, in minutes (30, 60, 90, 120, 180, 240) after the intervention. Method of measurement: Visual scale of pain.

Secondary

MeasureTime frame
Blood Pressure. Timepoint: 0,30,60,120,180,240 minutes after intervention. Method of measurement: MmHg With manometer.;Respiratory rate. Timepoint: 0,30,60,120,180,240 minutes after intervention. Method of measurement: Count the respiration rate.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahide Azarfar

Mazandaran University of Medical Sciences

azr1356@yahoo.com+98 11 3304 4866

Outcome results

None listed

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