Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT01078272 · ClinicalTrials.gov registry record · NA
The Saint Francis Remote Ischemic Preconditioning Trial (SaFR)
A NA study, sponsored by St. Francis Hospital, New York.
- Terminated
- Registry status
- NA
- Development phase
- 4
- Enrollment target
NCT01078272: Clinical Trial NA study, sponsored by St. Francis Hospital, New York.
NCT01078272 is a NA study that was terminated before completion, run by St. Francis Hospital, New York. The registered enrollment target is 4 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01078272, a NA study, was terminated before completion, sponsored by St. Francis Hospital, New York.
- TERMINATED
- Registry status
- NA
- Development phase
- 4 participants
- Enrollment target
Study Summary
This study tests the hypothesis that repeated inflation of a blood pressure cuff on the arm will improve results of coronary stent implantation by: * reducing chest pain and electrocardiogram changes during balloon inflation to place the stent * reducing leakage of heart muscle protein(troponin) into the blood stream after stent placement, indicated reduced damage to heart muscle during stent implantation * increases in molecules in the blood that promote dilation of arteries * reduced evidence of heart muscle damage on MRI immediately after stenting * improved patient outcomes over six months with fewer adverse cardiovascular events(heart attack, acute coronary syndrome,renarrowing of the stented artery, heart failure, death, stroke, transient ischemic attack) * improved heart structure and function at 6 months after stenting
Primary Outcome
MACE is defined as a combined endpoint including: heart attack, acute coronary syndrome,restenosis of the stented artery, new heart failure stroke, transient ischemic attack or death
Interventions
- OTHER Remote ischemic preconditioning
- OTHER Sham Remote Ischemic Preconditioning
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4 participants |
| Start Date | 2010-03 |
| Est. Completion | 2011-10 |
| Phase | NA |
Why NCT01078272 stopped before completion
NCT01078272 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 4 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 2 interventions - of which Remote ischemic preconditioning is the first listed.
NCT01078272 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01078272 about?
NCT01078272 is a clinical study titled "The Saint Francis Remote Ischemic Preconditioning Trial (SaFR)". This study tests the hypothesis that repeated inflation of a blood pressure cuff on the arm will improve results of coronary stent implantation by: * reducing chest pain and electrocardiogram changes during balloon inflation to place the stent * reducing leakage of heart muscle protein(troponin) in...
What is the current status of trial NCT01078272?
This trial is currently terminated. It is a NA study. The enrollment target is 4 participants. The study started on 2010-03. Estimated completion is 2011-10.
What interventions are being tested in trial NCT01078272?
The interventions under investigation include: Remote ischemic preconditioning (OTHER), Sham Remote Ischemic Preconditioning (OTHER).
Who is sponsoring clinical trial NCT01078272?
This trial is sponsored by St. Francis Hospital, New York, which has 5 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01078272's enrollment target sits among peer trials
4 1996th of 2000 higher than 5 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia