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TRPM8 Activators for Peripheral Neuropathy

12. mai 2026 oppdatert av: SHIANG-SUO HUANG

The Effect of Innovative TRPM8 Activators Membrane-Based Delivery System on Peripheral Neuropathy

The goal of this pilot prospective cohort study is to evaluate the efficacy of a novel hand and foot mask in alleviating symptoms of peripheral neuropathy caused by chemotherapy or diabetes. The study aims to determine whether regular use of these masks can improve patient comfort and quality of life.

The primary questions this study aims to answer are:

Does the use of the hand and foot mask reduce the severity of symptoms associated with chemotherapy-induced peripheral neuropathy (CIPN) or diabetic peripheral neuropathy (DPN)?

Does the application of the masks improve patient quality of life and treatment compliance for those undergoing chemotherapy?

Participants will:

Complete an initial assessment questionnaire on Day 1.

Apply hand and foot masks daily for 5 minutes, for 7 consecutive days.

Complete a follow-up questionnaire on Day 7 to assess the effects of one week of use.

Inclusion Criteria

Individuals are eligible for the study if they meet the following criteria:

Chemotherapy-Induced Peripheral Neuropathy (CIPN) group:

Age 20 or older.

Currently receiving or having previously received chemotherapy.

Demonstrating clinical signs and symptoms of chemotherapy-induced peripheral neuropathy.

Diabetic Peripheral Neuropathy (DPN) group:

Age 20 or older.

Diagnosed with diabetes mellitus.

Demonstrating clinical signs and symptoms of diabetic peripheral neuropathy.

General requirement:

Participants must be willing to participate and capable of signing the Informed Consent Form (ICF).

Studieoversikt

Detaljert beskrivelse

Peripheral neuropathy (PN) is a condition characterized by damage or dysfunction of the peripheral nerves, leading to sensory, motor, or autonomic impairments. Symptoms often include numbness, tingling, burning sensations, muscle weakness, and paresthesia. Chemotherapy-induced peripheral neuropathy (CIPN) and diabetic peripheral neuropathy (DPN) are two of the most prevalent causes of PN. Current pharmacological treatments, such as analgesics, anticonvulsants, antidepressants, and opioids, often provide limited efficacy and are frequently associated with significant adverse effects.

Study Rationale and Mechanism of Action:

The "Speedell" hand and foot mask is a novel product formulated to act primarily as a TRPM8 activator. TRPM8 is a non-selective cation channel with six transmembrane domains, widely expressed in human nerve cells. Upon activation by temperatures between 8-28°C or by specific agonists, TRPM8 generates cold signals that are transmitted to the somatosensory cortex.

Scientific literature suggests that the activation of TRPM8-whether by agonists or moderate cooling-induces the release of glutamate at central synapses. This glutamate subsequently activates inhibitory group II/III metabotropic glutamate receptors (mGluRs) located on injured nociceptive afferent neurons or postsynaptic receptors in the dorsal horn, thereby attenuating neuropathic hypersensitivity.

Furthermore, Speedell is designed to deliver natural cooling agents efficiently to the extremities, where they interact with TRPM8 receptors to provide immediate sensory relief. Evidence suggests that these components may contribute to the reduction of tissue damage caused by cellular inflammation. This pilot study aims to clinically validate the efficacy of the Speedell hand and foot mask in alleviating neuropathic discomfort and improving quality of life in patients suffering from chemotherapy-induced or diabetic peripheral neuropathy.

Studietype

Intervensjonell

Registrering (Faktiske)

60

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Taichung
      • Taichung, Taichung, Taiwan, 402306
        • Chung Shan Medical University Hospital

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

Inclusion Criteria:

  1. Patients aged 20 years or older who are currently receiving or have previously received chemotherapy and have clinical features of chemotherapy-induced peripheral neuropathy (CIPN).
  2. Diabetic patients aged 20 years or older who have clinical features of diabetic peripheral neuropathy (DPN).
  3. Patients who meet criteria 1 or 2, are willing to participate, and are able to sign an informed consent form.

Exclusion Criteria:

  1. Poorly controlled diabetes (HbA1c > 8%).
  2. Peripheral vascular disease.
  3. Chronic kidney disease (eGFR < 30 ml/min/m²).
  4. Depression, history of surgery on the hands, feet, or back.
  5. Skin conditions such as leprosy and connective tissue disorders, familial neuropathy.
  6. Pregnant or breastfeeding women.
  7. Individuals with allergic symptoms.
  8. Individuals with a history of convulsions.
  9. Individuals with G6PD deficiency (favism).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: behandling
Daily topical application for 5 minutes over 7 days

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in Norfolk Quality of Life Questionnaire-Diabetic Neuropathy (Norfolk QOL-DN) Score
Tidsramme: From baseline (Day 1) to the end of the treatment (Day 7).
The Norfolk QOL-DN is a validated instrument to assess the quality of life in patients with diabetic neuropathy. Scores range from 0 to 4 for each item, where 0 indicates "not at all" and 4 indicates "very much." A change in the total score will be calculated to measure the impact of the intervention.
From baseline (Day 1) to the end of the treatment (Day 7).
Change in European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-CIPN20) Score
Tidsramme: From baseline (Day 1) to the end of the treatment (Day 7).
The EORTC QLQ-CIPN20 is a specialized module for assessing chemotherapy-induced peripheral neuropathy symptoms. Scores range from 0 to 3 for each item, where 0 indicates "not at all" and 3 indicates "very much." A change in the total score will be calculated to measure the impact of the intervention.
From baseline (Day 1) to the end of the treatment (Day 7).

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Shiang-Suo Huang, PhD, Chung Shan Medical University

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

3. november 2025

Primær fullføring (Faktiske)

7. april 2026

Studiet fullført (Antatt)

1. juni 2026

Datoer for studieregistrering

Først innsendt

7. mai 2026

Først innsendt som oppfylte QC-kriteriene

7. mai 2026

Først lagt ut (Faktiske)

13. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

15. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

12. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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