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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03364842
Other study ID # Fuurosemide and coarctation
Secondary ID
Status Completed
Phase Phase 2
First received November 21, 2017
Last updated December 22, 2017
Start date November 22, 2017
Est. completion date December 20, 2017

Study information

Verified date December 2017
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

in our study the investigators give furosemide during surgery for repair of aortic coarctation via lateral thoracotomy and evaluated lung complications in comparison to control group


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date December 20, 2017
Est. primary completion date December 20, 2017
Accepts healthy volunteers No
Gender All
Age group 1 Month to 18 Months
Eligibility Inclusion Criteria:

- coarctation of aorta

Exclusion Criteria:

- heart failure, bleeding diathesis, associated cardiac congenital anomalies

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Furosemide
Administering furosemide

Locations

Country Name City State
Egypt Cairo university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary lung ultrasonography scale > 24 a 1 year study
Secondary Pao2/ Fio2 ratio a 1 year study
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