NCT00512811

Brief Summary

to assess the efficacy of inhaled furosemide in mustard gas exposed patients with acute respiratory failure

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

August 7, 2007

Completed
1 day until next milestone

First Posted

Study publicly available on registry

August 8, 2007

Completed
Last Updated

August 8, 2007

Status Verified

August 1, 2007

First QC Date

August 7, 2007

Last Update Submit

August 7, 2007

Conditions

Keywords

furosemideinhalationdyspneaspirometrymustard gasbronchiolitissulfur mustard

Outcome Measures

Primary Outcomes (1)

  • effect of furosemid inhalation on dyspnea

Interventions

Eligibility Criteria

Age32 Years - 83 Years
Sexmale
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Patients with a history of exposure to sulfur mustard with a complaint of dyspnea

You may not qualify if:

  • A contraindication for furosemide use;
  • An accompanying disease in which other drugs effective for dyspnea were used

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

RCCI

Tehran, Tehran Province, Iran

Location

MeSH Terms

Conditions

BronchiolitisRespiratory AspirationDyspnea

Interventions

Furosemide

Condition Hierarchy (Ancestors)

BronchitisRespiratory Tract InfectionsInfectionsBronchial DiseasesRespiratory Tract DiseasesLung Diseases, ObstructiveLung DiseasesRespiration DisordersPathologic ProcessesPathological Conditions, Signs and SymptomsSigns and Symptoms, RespiratorySigns and Symptoms

Intervention Hierarchy (Ancestors)

SulfanilamidesSulfonamidesAmidesOrganic ChemicalsAniline CompoundsAminesSulfonesSulfur Compounds

Study Officials

  • Mostafa Ghanei, MD

    Research Center of Chemical Injuries, Baqiyatallah Medical Science University, Tehran, Iran

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
CROSSOVER
Sponsor Type
OTHER

Study Record Dates

First Submitted

August 7, 2007

First Posted

August 8, 2007

Last Updated

August 8, 2007

Record last verified: 2007-08

Locations