BIIR Gene to Manage Heart Allograft Patients
NCT01929785 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 56
Last updated 2016-01-13
Summary
This is a single center observational study. Duration of the study is 1 year. Participants will be followed in 2 groups. Group 1 will include all patients who have undergone a heart transplant, through the first year post transplant. Group 2 will include heart transplant recipients from 1 year to 2 years post transplant. Groups will be enrolled simultaneously. It is anticipated each group will have 25 participants.
Conditions
- Cardiac Transplant Failure
Sponsors & Collaborators
-
Baylor Research Institute
lead OTHER
Principal Investigators
-
Shelley Hall, MD · Baylor Health Care System
Eligibility
- Min Age
- 18 Years
- Max Age
- 73 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-12-31
- Primary Completion
- 2013-11-30
- Completion
- 2013-11-30
Countries
- United States
Study Locations
More Related Trials
-
Aortic or Mitral Valve Replacement With the Braile Biomédica® Bovine Pericardium Valvular Bioprosthesis
NCT05902897 ·Status: COMPLETED
-
Prospective Balloon Aortic Valvuloplasty
NCT02122900 ·Status: COMPLETED
-
Evaluation of the Valiant Mona LSA Thoracic Stent Graft System in Descending TAA and Chronic Dissections
NCT02365467 ·Status: COMPLETED
-
ARISE: Evaluation of the GORE® Ascending Stent Graft in the Treatment of DeBakey Type I/II Aortic Dissection
NCT02380716 ·Status: COMPLETED
-
Endovascular Repair of Descending Thoracic Aortic Aneurysms
NCT00802984 ·Status: COMPLETED ·Phase: PHASE4
-
Safety Study of a Bioresorbable Coronary Stent
NCT01262703 ·Status: COMPLETED ·Phase: NA
-
Ankura™ TAA Stent Graft System Post-Market Clinical Follow-up Study
NCT05639569 ·Status: RECRUITING
-
DynamX Bioadaptor Global Post-Market Registry: Clinical Trial of the Elixir Medical DynamX Coronary Bioadaptor System
NCT06074549 ·Status: RECRUITING
-
BVS Implantation in Patients With Variant Angina and MODerate Coronary Artery Disease
NCT02932553 ·Status: WITHDRAWN ·Phase: PHASE4
-
Airway Bypass - Safety and Feasibility Study
NCT06249529 ·Status: RECRUITING ·Phase: EARLY_PHASE1
-
Study to Determine if the Valiant Stent Graft is Safe and Effective in Treating Patients Who Have a Blunt Thoracic Aortic Injury
NCT01092767 ·Status: COMPLETED ·Phase: NA
-
BioFreedom™ BA9™ Ultra
NCT05331547 ·Status: UNKNOWN
-
Bioresorbable Vascular Scaffolds Versus Stents in Patients With Chronic Total Occlusion
NCT02739685 ·Status: TERMINATED ·Phase: NA
-
Beacon Tip Sizing Catheter and Slip-Cath Beacon Tip Catheter Study
NCT06986954 ·Status: RECRUITING
-
The Bioresorbable Implants for Scaffolding Obstructions in Randomized Bifurcations (BIFSORB) Study
NCT02973529 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis in the Treatment of Type IV Thoracoabdominal Aortic Aneurysms
NCT02528500 ·Status: COMPLETED ·Phase: NA
-
A Prospective Single-Arm Multicenter StuDy of the BarE TEmporary SPur StEnt System foR the tREatment of Vascular Lesions Located in the infrapoplitEal Arteries beLow the Knee (DEEPER REVEAL)
NCT05358353 ·Status: COMPLETED ·Phase: NA
-
The BIFSORB Pilot Study II
NCT03027856 ·Status: COMPLETED ·Phase: NA
-
ReZolve2 Clinical Investigation
NCT01845311 ·Status: COMPLETED ·Phase: NA
-
PCI With AXXESS Biolimus A9 Eluting Bifurcation Stent in Treating Coronary Artery Bifurcation Disease
NCT02384629 ·Status: WITHDRAWN ·Phase: PHASE4
-
Clinical Study of the BARD® COVERA™ Arteriovenous (AV) Stent Graft in AV Graft Patients (AVeVA)
NCT02790606 ·Status: COMPLETED ·Phase: NA
-
BATwire Implant Kit
NCT04600791 ·Status: TERMINATED ·Phase: NA
-
Study on the Safety and Effectiveness of a Biodegradable Patent Foramen Ovale Occluder System
NCT07300358 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Multi-center Assessment of Grafts in Coronaries: Long-term Evaluation of the C-Port Device
NCT01478061 ·Status: COMPLETED ·Phase: PHASE4
-
Left Atrial Appendage Closure With SentreHeart Lariat® Device
NCT02681042 ·Status: COMPLETED ·Phase: NA