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NCT03966170 Clinical Trial

Citicoline as Neuroprotector in Preterm

Pre-Term Clinical Trial

Official title:
Efficacy of Citicoline as Neuroprotector in Preterm; A Randomized Controlled Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03966170
Other study ID # Citicoline
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date May 1, 2019
Est. completion date December 2028

Study information
Verified date May 2019
Source Tanta University
Contact Sherief Abd-Elsalam, ass. prof.
Phone 00201147773440
Email sheriefabdelsalam@yahoo.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Citicoline as neuroprotector in preterm

Description:

Efficacy of Citicoline as neuroprotector in preterm; A randomized controlled trial.

Recruitment information / eligibility
Status Recruiting
Enrollment 40
Est. completion date December 2028
Est. primary completion date November 2028
Accepts healthy volunteers No
Gender All
Age group N/A to 1 Month
Eligibility Inclusion Criteria:

- Preterm on CPAP or ventilator

Exclusion Criteria:

- Multiple congenital anomalies

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Citicoline
Citicoline as neuroprotector
• Placebo oral tablet
placebo drug

Locations
Country Name City State
Egypt Sherief Abd-Elsalam Tanta

Sponsors (1)
Lead Sponsor Collaborator
Sherief Abd-Elsalam

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of children with affection of the brain Number of children with affection of the brain 6 months
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