Bronchiolitis Clinical Trial
Official title:
Furosemide Inhalation in Dyspnea of Mustard Gas Exposed Patients: a Double-Blind Randomized Study
NCT number | NCT00512811 |
Other study ID # | 121a25 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | August 7, 2007 |
Last updated | August 7, 2007 |
Verified date | August 2007 |
Source | Baqiyatallah Medical Sciences University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Iran: Ethics Committee |
Study type | Interventional |
to assess the efficacy of inhaled furosemide in mustard gas exposed patients with acute respiratory failure
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | Male |
Age group | 32 Years to 83 Years |
Eligibility |
Inclusion Criteria: - Patients with a history of exposure to sulfur mustard with a complaint of dyspnea Exclusion Criteria: - A contraindication for furosemide use; - An accompanying disease in which other drugs effective for dyspnea were used |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
Iran, Islamic Republic of | RCCI | Tehran |
Lead Sponsor | Collaborator |
---|---|
Baqiyatallah Medical Sciences University |
Iran, Islamic Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | effect of furosemid inhalation on dyspnea |
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