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NCT06089135 · ClinicalTrials.gov registry record · NA

Shockwave Lithoplasty Compared to Cutting Balloon Treatment in Calcified Coronary Disease - A Randomized Controlled Trial

A NA study, sponsored by Baim Institute for Clinical Research.

Completed
Registry status
NA
Development phase
413
Enrollment target

NCT06089135 is a NA study that has completed, run by Baim Institute for Clinical Research. The registered enrollment target is 413 participants.

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The verdict

NCT06089135, a NA study, has completed, sponsored by Baim Institute for Clinical Research.

COMPLETED
Registry status
NA
Development phase
413 participants
Enrollment target

Study Summary

The Short-Cut trial is a prospective, investigator-initiated, multicenter, randomized controlled trial that is designed to compare the efficacy of cutting balloon angioplasty vs. intravascular lithotripsy prior to drug-eluting stent implantation in patients with moderate to severely calcified coronary arteries.

Interventions

  • DEVICE Intravascular Lithotripsy
  • DEVICE Cutting Balloon

Trial Details

FieldValue
Enrollment Target 413 participants
Start Date 2023-12-31
Est. Completion 2025-09-30
Phase NA

What the Registry Record Tells You About NCT06089135

The ClinicalTrials.gov registry entry for NCT06089135 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 413 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Baim Institute for Clinical Research, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Intravascular Lithotripsy is the first listed.

NCT06089135 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06089135 about?

NCT06089135 is a clinical study titled "Shockwave Lithoplasty Compared to Cutting Balloon Treatment in Calcified Coronary Disease - A Randomized Controlled Trial". The Short-Cut trial is a prospective, investigator-initiated, multicenter, randomized controlled trial that is designed to compare the efficacy of cutting balloon angioplasty vs. intravascular lithotripsy prior to drug-eluting stent implantation in patients with moderate to severely calcified corona...

What is the current status of trial NCT06089135?

This trial is currently completed. It is a NA study. The enrollment target is 413 participants. The study started on 2023-12-31. Estimated completion is 2025-09-30.

What interventions are being tested in trial NCT06089135?

The interventions under investigation include: Intravascular Lithotripsy (DEVICE), Cutting Balloon (DEVICE).

Who is sponsoring clinical trial NCT06089135?

This trial is sponsored by Baim Institute for Clinical Research, which has 7 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.