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Stibium Metallicum Praeparatum D6 Versus Placebo in the Reduction of Paclitaxel-induced Peripheral Neurotoxicity

Study acronym: STING-CIPN
StatusNot Yet Recruiting
PhasePhase 3
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 4 months later Aug 2028 → Jan 2029
Enrollment reduced 28% 120 → 86 participants
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Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Start date: Aug 2026 to Jan 2027 Show 8 more changesShow less
    • Primary completion pushed from Aug 2028 to Jan 2029
    • Enrollment reduced: 120 → 86 participants
    • Study completion pushed from Aug 2029 to Dec 2029
    • Eligibility criteria shortened, about 55 words
    • Secondary endpoints: 7 to 5
    • Study description shortened, about 18 words
    • Collaborators: 7 to 1
    • Study title revised
  2. Notable Primary completion date: Aug 2026 to Aug 2028
    • Start date: Aug 2025 to Aug 2026
    • Study completion date: Aug 2026 to Aug 2029
    • Collaborators revised (7)
    v7
  3. Notable Primary completion date: Aug 2024 to Aug 2026
    • Start date: Aug 2024 to Aug 2025
    • Study completion date: Aug 2025 to Aug 2026
    v6
  4. Notable Start date: Aug 2023 to Aug 2024v5
  5. Notable Primary completion date: Jan 2024 to Aug 2024
    • Start date: Jan 2023 to Aug 2023
    • Study completion date: Jan 2025 to Aug 2025
    v4
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  1. Notable Primary completion date: Feb 2022 to Jan 2024v3 Show 8 more changesShow less
    • Start date: Jan 2022 to Jan 2023
    • Enrollment target: 166 to 120
    • Study sites: 2 to 0
    • Study completion date: Jun 2024 to Jan 2025
    • Eligibility criteria revised
    • Study description shortened, about 3,273 words
    • Collaborators: 2 to 7
    • Study title shortened, about 4 words
  2. Notable Primary completion date: Jun 2023 to Feb 2022
    • Start date: May 2021 to Jan 2022
    • Study completion date: Oct 2023 to Jun 2024
    v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Chemotherapy induced peripheral neuropathy (CIPN) is one of the most limiting side effects of chemotherapy and often leads to adaptations in the protocol of the chemotherapy including dose reduction or even discontinuation of treatment. In general, the symptoms of CIPN are sensory, often distributed in a "stocking and glove" manner, and include pain, tingling, and numbness. CIPN has a marked negative influence on quality of life of patients and their families. It may result in serious limitations in daily functioning and affect the enjoyment, social relationships, and ability to perform work. Current management of CIPN (i.e. prevention and treatment) includes dose reduction or delay of chemotherapy cycles and treatment discontinuation. Unfortunately, this reduces the chance of an effective cancer treatment. Current guidelines of the American Society of Clinical Oncology (ASCO) on the Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy do not conclusively recommend any agent for the prevention of CIPN. Due to the scarcity of drugs that are effective for preventing and treating CIPN, the distress of patients who suffer from CIPN, and the major societal and economic costs, new approaches and effective treatment strategies are required. The proposed trial is a parallel, double blind, placebo controlled, randomised trial, aiming to determine whether treatment with SMP reduces the severity of symptoms of paclitaxel-induced peripheral neuropathy, as compared to placebo.
Trial Details
NCT Number NCT04715542
Lead Sponsor University of Bern
Collaborators: University Hospital, Basel, Switzerland
Conditions
(from sponsor)
Chemotherapy Induced Peripheral Neuropathy (CIPN)
Enrollment 86 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov