Clinical Trials Directory

Trials / Terminated

TerminatedNCT01406236

SAFE-PCI for Women

Study of Access Site for Enhancement of PCI for Women (SAFE-PCI for Women)

Status
Terminated
Phase
N/A
Study type
Interventional
Enrollment
1,787 (actual)
Sponsor
Duke University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The hypothesis of the SAFE-PCI for women trial is that, compared with transfemoral PCI, transradial PCI will result in a significant reduction in bleeding and vascular complications. The primary objective is to compare the efficacy and feasibility of the transradial approach to percutaneous coronary intervention (PCI) in women compared with the transfemoral approach. This study is a multicenter, randomized, open-label active controlled study. Three thousand women undergoing urgent or elective PCI from at least 50 centers will be randomized to either transradial or transfemoral PCI. Patients who are enrolled at sites performing ad hoc PCI will be randomized before diagnostic angiography. A total of approximately 3000 women will be randomized to obtain a cohort of approximately 1800 patients undergoing PCI. The Data Safety Monitoring Board has alerted us that the bleeding event rate overall in our trial is very low, making it unlikely that there will be statistical power to show a difference between the randomized arms in the SAFE PCI for Women study using the BARC bleeding definition per protocol. Based on this statistical futility, the DSMB has recommended stopping enrollment. They also noted, however, that as this is not based on any safety issues, and since there are a variety of key secondary endpoints (contrast and radiation exposure, quality of life) that are of clinical and scientific interest, the DSMB left it to the discretion of the Steering Committee to continue enrollment to meet sufficient power for these outcomes. On March 1, 2013, the Steering Committee met to discuss these issues and voted to continue enrollment until the planned sample size for the Quality of Life substudy was met (300 patients).

Conditions

Interventions

TypeNameDescription
PROCEDURETransradial PCITransradial PCI
PROCEDURETransfemoral PCITransfemoral PCI

Timeline

Start date
2011-08-01
Primary completion
2013-09-01
Completion
2013-09-01
First posted
2011-08-01
Last updated
2015-01-21

Source: ClinicalTrials.gov record NCT01406236. Inclusion in this directory is not an endorsement.