Multicenter LAser VA Registry of Percutaneous Coronary Interventions (LAVA)

Sponsor
North Texas Veterans Healthcare System (U.S. Fed)
Overall Status
Unknown status
CT.gov ID
NCT02789462
Collaborator
(none)
200

Study Details

Study Description

Brief Summary

This is a multi-center, investigator initiated study that will prospectively and retrospectively examine treatment strategies and outcomes of patients who underwent percutaneous coronary interventions (PCI).

The goal of this multi-center, investigator initiated, registry is to collect information on treatment strategies and outcomes of consecutive patients undergoing laser-assisted PCI among various participating centers. The study is a purely observational, chart review study and involves retrieval and compiling of data based on clinically indicated procedures and follow-up clinical and procedural outcomes.

The information collected will be used to determine the frequency of laser-assisted PCI performed at the participating sites and examine the procedural strategies utilized, and the procedural (both immediate and subsequent) outcomes.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Laser-assisted percutaneous coronary interventions

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
200 participants
Observational Model:
Case-Only
Time Perspective:
Other
Official Title:
Multicenter LAser VA Registry of Percutaneous Coronary Interventions (LAVA)
Study Start Date :
Jan 1, 2015
Actual Primary Completion Date :
Mar 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Patients undergoing laser-assisted PCI

Patients of VAMC centers who undergone laser-assisted percutaneous coronary interventions.

Procedure: Laser-assisted percutaneous coronary interventions
Chart review and data collection of patients undergoing laser-assisted percutaneous coronary interventions

Outcome Measures

Primary Outcome Measures

  1. Procedural success of the PCI [through hospital discharge post-PCI procedure, approximately 24 hours, but variable based on patient recovery.]

    Procedural success is defined as achievement of technical success with no in-hospital major adverse cardiac events (MACE). In-hospital MACE includes any of the following adverse events prior to hospital discharge: death from any cause, myocardial infarction, urgent repeat target vessel revascularization with PCI or coronary bypass surgery, tamponade requiring pericardiocentesis or surgery, or stroke.

Secondary Outcome Measures

  1. Technical success of the PCI [through end of PCI of procedure, approximately 5 minutes after end of procedure]

    Technical success of the PCI was defined as successful revascularization with achievement of <30% residual diameter stenosis within the treated segment and restoration of TIMI grade 3 antegrade flow.

  2. major adverse cardiovascular events [through hospital discharge post-PCI procedure,approximately 24 hours, but variable based on patient recovery.]

    In-hospital major adverse cardiovascular events (MACE) include any of the following adverse events prior to hospital discharge: death from any cause, myocardial infarction, urgent repeat target vessel revascularization with PCI or coronary bypass surgery, tamponade requiring pericardiocentesis or surgery, or stroke. MACE during clinical follow-up include death, myocardial infarction, target lesion and target vessel revascularization.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who have undergone/will be undergoing laser-assisted PCI at each of the participating centers during the study period.

  • Willing and able to provide informed consent.

Exclusion Criteria:
  • Not eligible candidate as per review by Investigator.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • North Texas Veterans Healthcare System

Investigators

  • Principal Investigator: Bavana Rangan, BDS, MPH, UT Southwestern Medical Center/ Dallas VA Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Bavana V. Rangan, Faculty Associate, Cardiology Research, North Texas Veterans Healthcare System
ClinicalTrials.gov Identifier:
NCT02789462
Other Study ID Numbers:
  • 15075
First Posted:
Jun 3, 2016
Last Update Posted:
Sep 13, 2017
Last Verified:
Sep 1, 2017
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2017