Ignite Creation Date:
2024-05-06 @ 2:38 AM
Last Modification Date:
2024-10-26 @ 11:21 AM
Study NCT ID:
NCT02098993
Status:
TERMINATED
Last Update Posted:
2019-07-16
First Post:
2014-03-25
Brief Title:
Feasibility Study of Unfractionated Heparin in Acute Chest Syndrome
Sponsor:
Craig Seaman
Organization:
University of Pittsburgh
Study Overview
Official Title:
Unfractionated Heparin in Acute Chest Syndrome A Pilot Feasibility Randomized Controlled Trial of Unfractionated Heparin vs Standard of Care in Acute Chest Syndrome
Status:
TERMINATED
Status Verified Date:
2019-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Poor enrollment
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this study is to determine the feasibility of performing a larger multicenter phase III trial to assess the effects of unfractionated heparin UFH in acute chest syndrome ACS Prespecified feasibility criteria consists of the ability to enroll potential study participants which includes the timely notification of hospitalized patients with ACS the capacity to consent eligible individuals and the ability to appropriately randomize eligible patients within 24 hours of diagnosis Additional feasibility objectives involve ensuring appropriate eligibility criteria proper administration of the study drug and the ability to completely and accurately collect clinical data of interest The final aim of our pilot study is to provide preliminary data with respect to treatment effect and variance to allow sample size calculation in a larger trial given the lack of data available to help guide this process The investigators hypothesize that the use of UFH in ACS will result in a decrease in the duration of hospitalization and improve other clinical outcomes such as the duration of hypoxemia and duration of moderate to severe pain
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
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?:
None