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NCT03630367 Clinical Trial

Effects of L-Carnitine Supplementation on Respiratory Distress Syndrome

Premature Birth Clinical Trial

Official title:
Effects of Adding L-Carnitine With Dexamethasone on Respiratory Distress Syndrome Development in Preterm Infants

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT03630367
Other study ID # LCPET
Secondary ID
Status Withdrawn
Phase Phase 4
First received
Last updated
Start date October 3, 2018
Est. completion date October 2020

Study information
Verified date April 2021
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the present study was to investigate the efficacy of L-carnitine therapy on the occurrence and prognosis of respiratory distress syndrome

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date October 2020
Est. primary completion date September 2020
Accepts healthy volunteers No
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Pregnant women between 30-37 weeks - singleton pregnancy Exclusion Criteria: - congenital malformed fetus - Extreme premature

Study Design

Related Conditions & MeSH terms

  • Premature Birth
  • Respiratory Distress Syndrome, Adult
  • Respiratory Distress Syndrome, Newborn

Intervention

Drug:
• Dexamethasone
Intramuscular injection 8 mg
• L-Carnitine 1G/5mL Injection
slow intravenous injection

Locations
Country Name City State
Egypt Ahmed Abbas Assiut Cairo

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary the mean difference in the Apgar score after birth Assessment of fetal general condition 1 minute
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