Viewing Study NCT00650858


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Study NCT ID: NCT00650858
Status: COMPLETED
Last Update Posted: 2017-12-11
First Post: 2007-12-26
Is NOT Gene Therapy: True
Has Adverse Events: True

Brief Title: Clinical Trial on Treatment of Intraventricular Hemorrhage
Sponsor: Johns Hopkins University
Organization:

Study Overview

Official Title: Clot Lysis: Evaluating Accelerated Resolution of Intraventricular Hemorrhage (IVH)
Status: COMPLETED
Status Verified Date: 2017-11
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: CLEAR IVH
Brief Summary: The specific objective of this trial is to determine the lowest dose and dose frequency possible with the best pharmacokinetic and safety profile and it's ability to remove a blood clot from the ventricular system.
Detailed Description: The purpose of this trial is to determine the efficacy and pharmacokinetics of intraventricular injections of multiple low doses of rt-PA. Sixteen subjects were already randomized to receive intraventricular injections of with 0.3 mg or 1.0 mg of rt-PA every 12 hours for up to 8 doses. Results of this stage (n=16) were then analyzed and the most effective dose of 1.0 mg was chosen to be used in the second stage (n=36) to determine the optimal frequency of dosing. We propose to test if this intervention facilitates more rapid clot resolution, complete recovery function and decreased mortality from this condition.

Study Oversight

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

Secondary ID Infos

Secondary ID Type Domain Link View
ISRCTN47341677 REGISTRY ISRCTN registry View