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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00512811
Other study ID # 121a25
Secondary ID
Status Completed
Phase Phase 3
First received August 7, 2007
Last updated August 7, 2007

Study information

Verified date August 2007
Source Baqiyatallah Medical Sciences University
Contact n/a
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Drug:
furosemide


Locations

Country Name City State
Iran, Islamic Republic of RCCI Tehran

Sponsors (1)

Lead Sponsor Collaborator
Baqiyatallah Medical Sciences University

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary effect of furosemid inhalation on dyspnea
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