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NCT01068119 · ClinicalTrials.gov registry record · Phase 4

Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplasty (PTCA)

A Phase 4 study, sponsored by Piedmont Healthcare.

Terminated
Registry status
Phase 4
Development phase
57
Enrollment target

NCT01068119: Clinical Trial Phase 4 study, sponsored by Piedmont Healthcare.

NCT01068119 is a Phase 4 study that was terminated before completion, run by Piedmont Healthcare. The registered enrollment target is 57 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01068119, a Phase 4 study, was terminated before completion, sponsored by Piedmont Healthcare.

TERMINATED
Registry status
Phase 4
Development phase
57 participants
Enrollment target

Study Summary

Same day discharge is safe and feasible in selected troponin negative patients undergoing coronary planned percutaneous coronary intervention (PCI) or ad hoc PCI via the transfemoral approach.

Interventions

  • PROCEDURE Same-day discharge

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2010-02
Est. Completion 2012-03
Phase Phase 4
Piedmont Healthcare

13 total trials

Why NCT01068119 stopped before completion

NCT01068119 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 57 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (89% lower).

The record links to 0 conditions, and to 1 intervention - of which Same-day discharge is the first listed.

NCT01068119 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01068119 about?

NCT01068119 is a clinical study titled "Same-Day Discharge After Coronary Percutaneous Transluminal Coronary Angioplasty (PTCA)". Same day discharge is safe and feasible in selected troponin negative patients undergoing coronary planned percutaneous coronary intervention (PCI) or ad hoc PCI via the transfemoral approach.

What is the current status of trial NCT01068119?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 57 participants. The study started on 2010-02. Estimated completion is 2012-03.

What interventions are being tested in trial NCT01068119?

The interventions under investigation include: Same-day discharge (PROCEDURE).

Who is sponsoring clinical trial NCT01068119?

This trial is sponsored by Piedmont Healthcare, which has 13 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01068119's enrollment target sits among peer trials

57 1209th of 2000 higher than 788 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

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Source: ClinicalTrials.gov NCT01068119, the US trial registry maintained by the National Library of Medicine. NCT01068119 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.