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NCT07142304 · ClinicalTrials.gov registry record · NA

The Lilac Device Trial

A NA study of Chemotherapy Induced Peripheral Neuropathy (CIPN), sponsored by Luminate Medical.

Recruiting
Registry status
NA
Development phase
142
Enrollment target
8
Study locations

NCT07142304 is a NA study of Chemotherapy Induced Peripheral Neuropathy (CIPN) that is actively recruiting participants, run by Luminate Medical. The registered enrollment target is 142 participants. The trial reports 8 study locations across 7 states.

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The verdict

NCT07142304, a NA study of Chemotherapy Induced Peripheral Neuropathy (CIPN), is actively recruiting participants, sponsored by Luminate Medical.

RECRUITING
Registry status
NA
Development phase
142 participants
Enrollment target
8
Study locations

Study Summary

Chemotherapy drugs, used in the treatment of cancer, have the potential of inducing peripheral neuropathy (PN) as a side effect. This side effect is commonly referred to as CIPN, or chemotherapy-induced peripheral neuropathy. The Lilac Glove and Boot devices apply a low pressure across the surface of the hands and feet, respectively, to reduce access of chemotherapy to the peripheral nerves on the hands and feet. The small amount of pressure reduces the level of chemotherapy reaching the peripheral nerves, hence increasing the likelihood of nerve preservation during treatment and thus may potentially temporarily prevent the onset of moderate to severe PN symptoms induced by chemotherapy in the hands and feet while receiving treatment

Interventions

  • DEVICE Sham device
  • DEVICE The Lilac Device

Study Locations (8)

Ohio

  • Springfield Regional Cancer Center - Springfield
  • Mercy Health St. Elizabeth Hospital - Youngstown

California

  • Palomar Medical Center Poway - Poway

Florida

  • Hialeah Hospital - Hialeah

Hawaii

  • Hawaii Cancer Care - Honolulu

Illinois

  • Hope and Healing Cancer Services - Hinsdale

Minnesota

  • Health Partners Frauenshuh Cancer Center - Minneapolis

Wisconsin

  • Hospital Sisters Health System - St.Vincent & St.Mary's - Green Bay

Trial Details

FieldValue
Enrollment Target 142 participants
Start Date 2025-10-03
Est. Completion 2026-10
Phase NA

Sponsor

Luminate Medical

2 total trials

What the Registry Record Tells You About NCT07142304

The ClinicalTrials.gov registry entry for NCT07142304 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 142 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Luminate Medical, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chemotherapy Induced Peripheral Neuropathy (CIPN) appearing as the primary indexed condition, and to 2 interventions - of which Sham device is the first listed.

NCT07142304 reports 8 study locations spanning 7 distinct geographic areas - top geographies include Ohio, California, Florida.

Frequently Asked Questions

What is clinical trial NCT07142304 about?

NCT07142304 is a clinical study titled "The Lilac Device Trial". Chemotherapy drugs, used in the treatment of cancer, have the potential of inducing peripheral neuropathy (PN) as a side effect. This side effect is commonly referred to as CIPN, or chemotherapy-induced peripheral neuropathy. The Lilac Glove and Boot devices apply a low pressure across the surface ...

What is the current status of trial NCT07142304?

This trial is currently recruiting. It is a NA study. The enrollment target is 142 participants. The study started on 2025-10-03. Estimated completion is 2026-10.

What conditions does trial NCT07142304 study?

This clinical trial studies the following conditions: Chemotherapy Induced Peripheral Neuropathy (CIPN).

What interventions are being tested in trial NCT07142304?

The interventions under investigation include: Sham device (DEVICE), The Lilac Device (DEVICE).

Who is sponsoring clinical trial NCT07142304?

This trial is sponsored by Luminate Medical, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07142304 being conducted?

This trial has 8 study locations across California, Florida, Hawaii, Illinois, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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