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COMPLETED Phase 2

Safety and Efficacy of NTX-001 Compared to SOC in Acute Single Peripheral Nerve Injuries

NCT04572906 · View on ClinicalTrials.gov ↗

Study Summary

NTX-001 is a single use surgical product intended for use in conjunction with standard suture neurorrhaphy of severed nerves in patients between 16 and 80 years of age.

Conditions Studied

Interventions

  • COMBINATION_PRODUCT NTX-001

Study Locations (10)

Florida

  • UF Health - University of FL - Gainesville — Gainesville
  • Orlando Health — Orlando

Maryland

  • Curtis National Hand Center — Baltimore
  • Johns Hopkins Bayview Medical Center — Baltimore

Illinois

  • University of Chicago — Chicago

Indiana

  • Indiana Hand to Shoulder Center — Indianapolis

Missouri

  • Washington University — St Louis

Ohio

  • The Ohio State University Wexner Medical Center Hand and Upper Extremity Center — Columbus

Virginia

  • Virginia Commonwealth University — Richmond

Washington

  • Harborview Medical Center — Seattle

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2020-09-25
Est. Completion 2024-06-27
Phase Phase 2

Sponsor

Neuraptive Therapeutics

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04572906

The ClinicalTrials.gov registry entry for NCT04572906 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neuraptive Therapeutics, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Peripheral Nerve Injuries appearing as the primary indexed condition, and to 1 intervention — of which NTX-001 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT04572906 reports 10 study locations spanning 8 distinct geographic areas — top geographies include Florida, Maryland, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT04572906 about?

NCT04572906 is a clinical study titled "Safety and Efficacy of NTX-001 Compared to SOC in Acute Single Peripheral Nerve Injuries". NTX-001 is a single use surgical product intended for use in conjunction with standard suture neurorrhaphy of severed nerves in patients between 16 and 80 years of age.

What is the current status of trial NCT04572906?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 51 participants. The study started on 2020-09-25. Estimated completion is 2024-06-27.

What conditions does trial NCT04572906 study?

This clinical trial studies the following conditions: Peripheral Nerve Injuries. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04572906?

The interventions under investigation include: NTX-001 (COMBINATION_PRODUCT). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04572906?

This trial is sponsored by Neuraptive Therapeutics, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04572906 being conducted?

This trial has 10 study locations across Florida, Illinois, Indiana, Maryland, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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