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comparison of effects of nebulised Frusemide and placebi in patients with acute dyspnea transmited by EMS

comparison of effects of nebulised Frusemide and placebi in patients with acute dyspnea transmited by EMS

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171014036753N2
Enrollment
150
Registered
2019-01-08
Start date
2018-11-26
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

acute dyspnea. Dyspnea

Interventions

Intervention 1: Intervention group: 40 milligram of Furosemide is inhaled through nebulizer in addition to routine treatment in ambulances. Intervention 2: Control group: Normal Saline as a placebo wi

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: all patient between 18 to 75 years old with dyspnea who transmitted to hospitals by EMS

Exclusion criteria

Exclusion criteria: not willing to participate in the study history of susceptibility to sulfa drugs unstable hemodynamics; requiring mechanical ventilation; decreased consciousness, accompany with another illness requiring treatment in the first 10 minutes of treatment with digoxin, beta blocker, beta-agonist and calcium; need to have another inhaling treatment in the first 10 minutes and need to have non-invasive ventilation.

Design outcomes

Primary

MeasureTime frame
Oxygen saturation. Timepoint: baseline until arrive to hospital. Method of measurement: Pulse oximeter.;MMRC Dyspnea Severity Scale. Timepoint: baseline until arrive to hospital. Method of measurement: Visual Analouge Scale.

Secondary

MeasureTime frame
Severity of dyspnea. Timepoint: baseline until to arrive to hospital. Method of measurement: visual analogue scale by EMS staff.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBabak Mahshidfar

Iran University of Medical Sciences

mahshidfar.b@iums.ac.ir+98 21 86701

Outcome results

None listed

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