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Citicoline in Ischemic Stroke, a Randomized Trial - Trial NCT06210646

Access comprehensive clinical trial information for NCT06210646 through Pure Global AI's free database. This Phase 3 trial is sponsored by Kafrelsheikh University and is currently Recruiting. The study focuses on Ischemic Stroke. Target enrollment is 800 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06210646
Phase 3
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06210646
View on ClinicalTrials.gov
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Citicoline in Ischemic Stroke, a Randomized Trial
Citicoline in Ischemic Stroke, a Randomized Placebo-controlled Trial

Study Focus

Ischemic Stroke

Citicoline

Interventional

drug

Sponsor & Location

Kafrelsheikh University

Kafr Ash Shaykh, Egypt

Timeline & Enrollment

Phase 3

Dec 29, 2023

Dec 29, 2024

800 participants

Primary Outcome

Value of Montreal Cognitive Assessment (MoCA),Rate of drug-related complications after 6 months

Summary

Along with the current clinical trial, the efficacy and safety of a 1000 mg daily citicoline
 administered within 24 hours of the first-ever ischemic stroke and lasted 12 months compared
 to placebo were assessed through MoCA, NIHSS, mRS, and possible adverse effects.

ICD-10 Classifications

Stroke, not specified as haemorrhage or infarction
Sequelae of stroke, not specified as haemorrhage or infarction
Cerebral infarction
Cerebral infarction, unspecified
Other cerebral infarction

Data Source

ClinicalTrials.gov

NCT06210646

Non-Device Trial