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NCT05357469 · ClinicalTrials.gov registry record · NA

Innovative Treatment of Chemotherapy-Induced Painful Peripheral Neuropathy in Adolescents and Young Adults With Cancer: A Two Arm Pilot Study

A NA study of Peripheral Neuropathy, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
NA
Development phase
38
Enrollment target
1
Study location

NCT05357469 is a NA study of Peripheral Neuropathy that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 38 participants, below the 79-participant average among 27 other Peripheral Neuropathy trials with a reported enrollment target (52% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05357469, a NA study of Peripheral Neuropathy, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

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

Study Summary

To evaluate the efficacy and safety of Scrambler therapy (ST) for chemotherapy-induced painful peripheral neuropathy (CIPN), and the impact of ST on physical functioning and quality of life (QoL) in adolescents and young adults (AYA) cancer patients. In this proposed study, we will conduct a two-arm prospective, randomized wait-list controlled clinical trial to investigate the effectiveness of ST on pain and CIPN in AYAs with cancer.

Conditions Studied

Interventions

  • DEVICE Immediate St (Scrambler Therapy)
  • DEVICE Waitlist ST (Scrambler Therapy)

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2022-07-14
Est. Completion 2026-07-31
Phase NA

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT05357469

The ClinicalTrials.gov registry entry for NCT05357469 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 79-participant average among 27 other Peripheral Neuropathy trials with a reported enrollment target (52% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Peripheral Neuropathy appearing as the primary indexed condition, and to 2 interventions - of which Immediate St (Scrambler Therapy) is the first listed.

NCT05357469 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05357469 about?

NCT05357469 is a clinical study titled "Innovative Treatment of Chemotherapy-Induced Painful Peripheral Neuropathy in Adolescents and Young Adults With Cancer: A Two Arm Pilot Study". To evaluate the efficacy and safety of Scrambler therapy (ST) for chemotherapy-induced painful peripheral neuropathy (CIPN), and the impact of ST on physical functioning and quality of life (QoL) in adolescents and young adults (AYA) cancer patients. In this proposed study, we will conduct a two-ar...

What is the current status of trial NCT05357469?

This trial is currently recruiting. It is a NA study. The enrollment target is 38 participants. The study started on 2022-07-14. Estimated completion is 2026-07-31.

What conditions does trial NCT05357469 study?

This clinical trial studies the following conditions: Peripheral Neuropathy.

What interventions are being tested in trial NCT05357469?

The interventions under investigation include: Immediate St (Scrambler Therapy) (DEVICE), Waitlist ST (Scrambler Therapy) (DEVICE).

Who is sponsoring clinical trial NCT05357469?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05357469 being conducted?

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

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

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