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NCT03208894 Clinical Trial

Role of Salbutamol and Furosemide in TTN

Transient Tachypnea of the Newborn Clinical Trial

Official title:
Role of Salbutamol and Furosemide in Transient Tachypnea of Newborn

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03208894
Other study ID # TTN
Secondary ID
Status Completed
Phase Phase 3
First received July 1, 2017
Last updated July 5, 2017
Start date November 1, 2016
Est. completion date June 30, 2017

Study information
Verified date July 2017
Source Armed Forces Hospital, Pakistan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

to see the effects of slabutamol and IV furosemide in the treatment of transient tachypnea of newborn

Recruitment information / eligibility
Status Completed
Enrollment 100
Est. completion date June 30, 2017
Est. primary completion date May 30, 2017
Accepts healthy volunteers No
Gender All
Age group N/A to 7 Days
Eligibility Inclusion Criteria:

- all newborn babies with clinically diagnosed TTN

Exclusion Criteria:

- babies less than 34 weeks babies with congenital malformations and CHD

Study Design

Related Conditions & MeSH terms

  • Tachypnea
  • Transient Tachypnea of the Newborn

Intervention

Drug:
• Furosemide Injection
efficacy of salbutamol and furosemide in TTN

Locations
Country Name City State
Pakistan Department of Pediatrics Rawalpindi Punjab
Pakistan Military Hospital Rawalpindi Punjab

Sponsors (1)
Lead Sponsor Collaborator
Armed Forces Hospital, Pakistan

Country where clinical trial is conducted

Pakistan, 

Outcome
Type Measure Description Time frame Safety issue
Primary duration of oxygen requiremment in neonates having TTN. neonates will be subjected to treatment with furosemide and sabutamol and the duration of oxygen dependecy will be assessed. upto 6 months
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