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The effect of morphine with nebulizer mask in the treatment of acute respiratory distress in adult patients with Covid-19

Evaluation of efficacy and safety of morphine through nebulizer mask in the treatment of acute respiratory distress due to Covid-19 in adult patients

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211112053042N2
Enrollment
60
Registered
2021-12-06
Start date
2021-12-20
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Acute respiratory distress caused by Covid-19. Coronavirus as the cause of diseases classified to other chapters

Interventions

Intervention 1: Intervention group: Patients receive morphine with a nebulizer mask immediately after admission to the ward or emergency room. Intervention 2: Control group: Patients receive normal sa

Sponsors

Karaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age 80-18 years Patients with a definitive diagnosis of Covid-19 based on PCR test within 48 hours after hospitalization Acute moderate respiratory distress syndrome with PaO2 / FiO2 <200 based on Berlin criteria (Force et al., 2012) Patients with severe dyspnea Patients in the end-stages of the disease Lack of proper treatment Patients with consent to participate in the project

Exclusion criteria

Exclusion criteria: Patients with high suspicion / diagnosis of heart failure and unstable angina Existence of severe shock with hemodynamic instability despite increased vascular pressure Severe / undiagnosed lung infection for other reasons (chronic obstructive pulmonary disease, pulmonary fibrosis, lung cancer, bacterial pneumonia ...) Diagnosis of pulmonary hemorrhage Pregnancy / breastfeeding An important cause other than acute respiratory distress for respiratory failure Requires ECMO during the study period He/she is expected to be transferred to another hospital within 72 hours Known allergies to morphine Sensitivity or contraindication to exogenous and endogenous opioids Obesity (BMI>35 kg/m2 ) Patients with dissatisfaction with participating in the project

Design outcomes

Primary

MeasureTime frame
Mortality rate. Timepoint: During hospitalization. Method of measurement: Based on the patient's record.

Secondary

MeasureTime frame
Oxygen saturation level. Timepoint: Morphine dose before titration, 2 hours after first titration, 2 hours after second titration, 2 hours after third titration, 2 hours after effective drug titration, 12 hours after effective drug titration, 24 hours after effective drug titration. Method of measurement: Pulse oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Hossein Delshad MD.

Karaj University of Medical Sciences

m.delshad@abzums.ac.ir+98 26 3350 2347

Outcome results

None listed

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