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Comparison the effect of intranasal ketamine hydrochloride and intravenous morphine sulfate on pain severity of patients with upper or lower limbs fracture

Comparsion the effect of intranasal ketamine hydrochloride and intravenous morphine sulfate on pain severity of patients with limb fracture

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016031027007N1
Enrollment
104
Registered
2016-05-28
Start date
2016-03-20
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. Pain in limb

Interventions

Intervention 1: Patients in intranasal ketamine hydrochloride group will receive 1 mg/kg ketamine hydrochloride of 10 ml solution (which put in sterile nasal drop bottle) via inhalation. Intervention
Treatment - Drugs
Patients in intranasal ketamine hydrochloride group will receive 1 mg/kg ketamine hydrochloride of 10 ml solution (which put in sterile nasal drop bottle) via inhalation.
Patients in intravenous morphine sulfate group will receive 0.1 mg/kg morphine sulfate via intravenous

Sponsors

Vice chancellor for research, Ahwaz Judishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age range of 15 to 64 years; having upper and lower limbs fracture. Exclusion criteria: low of consciousness; hemodynamic instability; addiction to drugs or opioids; mental retardation and psychosis; chronic cardiovascular diseases; being pregnant and breastfeeding; intranasal ketamine hydrochloride and intravenous morphine sulfate contraindication.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: Before intervention and 5, 10, 15, 20, 25 and 30 minutes after intervention. Method of measurement: Visual analog scale.

Secondary

MeasureTime frame
Vital sign. Timepoint: Before intervention and 5, 10, 15, 20, 25 and 30 minutes after intervention. Method of measurement: Cardiopulmonary monitoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayyeh Gharibi

Ahvaz Imam Khomeini hospital

Dr.s.gharibi@gmail.com+98 61 3222 2922

Outcome results

None listed

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