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NCT06813430 · ClinicalTrials.gov registry record · NA

Non-Contact Low-Frequency Ultrasound Vs Standard LaLonde Protocol for Fingertip Injury Wound Healing

A NA study of Non-contact Low Frequency Ultrasound and Lalonde Protocol, sponsored by St. Luke's Hospital, Pennsylvania.

Recruiting
Registry status
NA
Development phase
22
Enrollment target
1
Study location

NCT06813430 is a NA study of Non-contact Low Frequency Ultrasound and Lalonde Protocol that is actively recruiting participants, run by St. Luke's Hospital, Pennsylvania. The registered enrollment target is 22 participants. The trial reports 1 study location across 1 state.

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The verdict

NCT06813430, a NA study of Non-contact Low Frequency Ultrasound and Lalonde Protocol, is actively recruiting participants, sponsored by St. Luke's Hospital, Pennsylvania.

RECRUITING
Registry status
NA
Development phase
22 participants
Enrollment target
1
Study location

Study Summary

The goal of this clinical trial is to compare the efficacy of non-contact low frequency ultrasound in populations sustaining fingertip amputations. The main question it aims to answer is: • Does non-contact low frequency ultrasound significantly improve patient outcomes in patients sustaining acute fingertip amputations? Researchers will compare non-contact low frequency ultrasound to a standard Lalonde protocol to answer this questions. Participants will be randomized one of the two study arms and evaluated by wound care therapy. They will receive cohort appropriate therapy sessions 2-3 times per week with measurement of wound size once per week.

Interventions

  • DEVICE Non-contact Low Frequency Ultrasound
  • OTHER Lalonde Protocol (standard of care)

Study Locations (1)

Pennsylvania

  • St. Luke's University Health Network - Bethlehem

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2025-02-10
Est. Completion 2026-02
Phase NA

Sponsor

St. Luke's Hospital, Pennsylvania

10 total trials

What the Registry Record Tells You About NCT06813430

The ClinicalTrials.gov registry entry for NCT06813430 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Luke's Hospital, Pennsylvania, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Non-contact Low Frequency Ultrasound appearing as the primary indexed condition, and to 2 interventions - of which Non-contact Low Frequency Ultrasound is the first listed.

NCT06813430 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT06813430 about?

NCT06813430 is a clinical study titled "Non-Contact Low-Frequency Ultrasound Vs Standard LaLonde Protocol for Fingertip Injury Wound Healing". The goal of this clinical trial is to compare the efficacy of non-contact low frequency ultrasound in populations sustaining fingertip amputations. The main question it aims to answer is: • Does non-contact low frequency ultrasound significantly improve patient outcomes in patients sustaining acute...

What is the current status of trial NCT06813430?

This trial is currently recruiting. It is a NA study. The enrollment target is 22 participants. The study started on 2025-02-10. Estimated completion is 2026-02.

What conditions does trial NCT06813430 study?

This clinical trial studies the following conditions: Non-contact Low Frequency Ultrasound, Lalonde Protocol, Fingertip Amputation.

What interventions are being tested in trial NCT06813430?

The interventions under investigation include: Non-contact Low Frequency Ultrasound (DEVICE), Lalonde Protocol (standard of care) (OTHER).

Who is sponsoring clinical trial NCT06813430?

This trial is sponsored by St. Luke's Hospital, Pennsylvania, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06813430 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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.