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The effect of morphine in reducing pain

Comparison of the complications and pain relieving of nebulized morphine and intravenous morphine in trauma patients with musculoskeletal pain.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017011431931N1
Enrollment
240
Registered
2017-06-13
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

pain. Acute pain

Interventions

Intervention 1: Intervention group 1: 1.0 mg/kg of diluted morphine will be administered intravenously and 5 cc of sterile water will be given via nebulizer as placebo. Pain and drug side effects will
Treatment - Drugs
Intervention group 1: 1.0 mg/kg of diluted morphine will be administered intravenously and 5 cc of sterile water will be given via nebulizer as placebo. Pain and drug side effects will be evaluated 0,
Intervention group 2: 2.0 mg/kg of nebulized morphine sulfate is administered via facemask, and 5 cc of sterile water is given via nebulizer as placebo. Pain and drug side effects will be evaluated 0,
Intervention group 3: 4.0 mg/kg of nebulized morphine sulfate is administered via facemask and 5 cc of sterile water is given via nebulizer as placebo. Pain and drug side effects will be evaluated 0,

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were: age between 18 and 65 years; severe acute musculoskeletal pain between 6 and 10 on VAS. Exclusion criteria: Consent to participate in research projects; Drug addiction; Systolic blood pressure less than 90 mmHg; GCS less than 15; Heart, lung, kidney, liver or mental diseases; Pregnancy and lactation; Known hypersensitivity to morphine and ketamine.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 0, 15 , 30, 45 and 60 minutes after intervention. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Hypotension. Timepoint: 0, 15, 30, 45 and 60 minutes after intervention. Method of measurement: Blood pressure cuff.;Apnea. Timepoint: 0 , 15, 30, 45 ,and 60 minutes after intervention. Method of measurement: puls oximetry.;Oxygen saturation. Timepoint: 0 , 15, 30, 45 , and 60 minutes after intervention. Method of measurement: puls oximetry.;Nausea and vomiting. Timepoint: 0 , 15, 30, 45 and 60 minutes after intervention. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Ali Dashti

Iran University of Medical Sciences

Dr.Dashti82@gmail.com+98 21 4462 6024

Outcome results

None listed

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