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NCT06616649 · ClinicalTrials.gov registry record · NA

Closed Loop Spinal Cord Stimulation for Chemotherapy Induced Peripheral Neuropathy, a Pilot Study.

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

Recruiting
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT06616649: Recruiting NA study of Peripheral Neuropathy Due to Chemotherapy, sponsored by M.D. Anderson Cancer Center.

NCT06616649 is a NA study of Peripheral Neuropathy Due to Chemotherapy that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 10 participants, below the 59-participant average among 6 other Peripheral Neuropathy Due to Chemotherapy trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06616649, a NA study of Peripheral Neuropathy Due to Chemotherapy, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

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

Study Summary

To explore the benefits of using closed loop spinal cord stimulation (SCS) in the treatment of patients experiencing painful chemotherapy induced peripheral neuropathy (CIPN) by assessing changes in pain, quality of life, pain medication use, sensory improvement through quantitative sensory testing, and improvement of gait through quantitative gait testing.

Interventions

  • DEVICE Spinal cord stimulator implant

Study Locations (1)

Texas

  • The University of Texas MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2025-07-14
Est. Completion 2027-07-01
Phase NA
M.D. Anderson Cancer Center

2,692 total trials

What NCT06616649 shows while recruiting

NCT06616649 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 59-participant average among 6 other Peripheral Neuropathy Due to Chemotherapy trials with a reported enrollment target (83% lower).

The record links to 1 condition, with Peripheral Neuropathy Due to Chemotherapy appearing as the primary indexed condition, and to 1 intervention - of which Spinal cord stimulator implant is the first listed.

NCT06616649 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT06616649 about?

NCT06616649 is a clinical study titled "Closed Loop Spinal Cord Stimulation for Chemotherapy Induced Peripheral Neuropathy, a Pilot Study.". To explore the benefits of using closed loop spinal cord stimulation (SCS) in the treatment of patients experiencing painful chemotherapy induced peripheral neuropathy (CIPN) by assessing changes in pain, quality of life, pain medication use, sensory improvement through quantitative sensory testing,...

What is the current status of trial NCT06616649?

This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2025-07-14. Estimated completion is 2027-07-01.

What conditions does trial NCT06616649 study?

This clinical trial studies the following conditions: Peripheral Neuropathy Due to Chemotherapy.

What interventions are being tested in trial NCT06616649?

The interventions under investigation include: Spinal cord stimulator implant (DEVICE).

Who is sponsoring clinical trial NCT06616649?

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

Where is trial NCT06616649 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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Source: ClinicalTrials.gov NCT06616649, the US trial registry maintained by the National Library of Medicine. NCT06616649 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.