Viewing Study NCT06353334



Ignite Creation Date: 2024-05-06 @ 8:22 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06353334
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-09
First Post: 2024-04-02

Brief Title: Butylphthalides Safety and Efficacy for Improving Neurological Function Prognosis in Patients With Cardiac Arrest BNCA Trial
Sponsor: Tang Ziren
Organization: Capital Medical University

Study Overview

Official Title: Butylphthalides Safety and Efficacy for Improving Neurological Function Prognosis in Patients With Cardiac Arrest BNCA Trial A Single-Center Randomized Double-Blind Placebo-Controlled Study
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Butylphthalide NBP is a neuroprotective medication capable of ameliorating neurological dysfunction induced by ischemia hypoxia and reperfusion injury in the brain However evidence regarding the improvement of neurological function prognosis in patients with return of spontaneous circulation ROSC after cardiac arrest CA by NBP is limited This study aims to evaluate the safety and efficacy of NBP treatment in improving the neurological function prognosis of patients with ROSC after CAThe study will be a single-center randomized double-blind placebo-controlled trial The sample size is estimated to be 100 patients Eligible patients will be randomly allocated in a 11 ratio to receive either NBP or placebo treatment daily for a duration of 14 days The initial administration of NBP or placebo treatment will commence within 6 hours after ROSC following CA The primary outcome is the proportion of patients with Cerebral Performance Category CPC scores of 1-2 at 90 days after randomization in each group The primary safety outcome is the percentage of severe adverse events occurring during the 14-day treatment period This trial will determine the efficacy of NBP in providing neuroprotective effects for patients with ROSC after CA
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None