About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 18
Early breast cancer, ovarian cancer or other gynecological cancer
Patients who are about to receive a treatment with paclitaxel for 12 or 18 weeks (weekly or three-weekly) as part of adjuvant or neo-adjuvant chemotherapy.
Ability to provide informed consent as documented by signature
Disqualifiers
Patients with pre-existing neuropathy
Prior chemotherapy with taxanes or other neurotoxic agents
Concomitant medications that are known to cause neuropathy
Pregnancy or lactation
Trial design
Parallel
Treatments tested in this trial
Stibium metallicum praeparatum 6x
DrugStibium metallicum praeparatum D6 will be administered with subcutaneous injections 3 times a week at 1 ampoule at 1 mL during the chemotherapy and shall be continued during 6 weeks after the end of chemotherapy . The first injection will be administered on the day of the first dose of chemotherapy, before the injection of the first dose of chemotherapy.
Placebo
DrugPlacebo will be administered with subcutaneous injections 3 times a week at 1 ampoule at 1 mL during the chemotherapy and shall be continued during 6 weeks after the end of chemotherapy . The first injection will be administered on the day of the first dose of chemotherapy, before the injection of the first dose of chemotherapy.
Treatment groups
Trial outcomes
Primary outcomes
Reduction in neuropathy severity
Measured by the neurotoxicity subscale (NTX-subscale) of the FACT/GOG-NTX questionnaire (FACT/GOG-NTX: Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity, Score rage of NTX-subscale: 0-44, the higher the score, the better the QOL)
Secondary outcomes
Occurrence and severity of paclitaxel-induced peripheral neuropathy over the whole study period
Measured by the NTX-subscale of the FACT/GOG-NTX questionnaire
Oncologist's evaluation CIPN
Assessed by oncologist using the CTCAE grading system
Chemotherapy adherence
Record whether all chemotherapy cycles could be administered as planned (indicate chemotherapy interruptions, dose reductions and discontinuations)
Effect on Quality of life (QOL)
Assessed by the FACT-G questionnaire (FACT-G: Functional Assessment of Cancer Therapy - General, Score range: 0-108, the higher the score, the better the QOL)
Other outcomes
Adherence to study medication (I)
Assessed by self-report
Adherence to study medication (II)
Assessed by returned unused medication
Severe adverse events
Recorded incidence and severity of adverse events
Locations
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Bern
Lead sponsor
University Hospital, Basel, Switzerland
Collaborator
This trial is not recruiting at the moment. You can still explore other options: