Efficacy and Tolerability of AP707 in Patients with chronic Pain due to traumatic or post-operative peripheral Neuropathy
- Conditions
- Chronic Pain due to traumatic or post-operative peripheral NeuropathyTherapeutic area: Diseases [C] - Pathological Conditions, Signs and Symptoms [C23]
- Registration Number
- CTIS2022-500898-13-00
- Lead Sponsor
- Cannaxan GmbH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 558
Signed and dated informed consent form, Patients with chronic pain due to traumatic or post-operative peripheral Neuropathy since at least 3 months, Female and male patients (= 18 years), Patients with more than 1 year life expectancy, Patients with optimized sCPT on study entry as defined in section 3.1.1 and section 3.1.3 of the study protocol, Willingness of study patients of both sexes to use reliable contraception during study participation and for three months after taking the last study medication, Good command of German language, in order to understand questionnaires in German, Current moderate to severe pain with pain intensity = 5 on Numeric Rating Scale (NRS, 0 - 10) and thus an existing need for further pain therapy, Completed QUISS (Quantification Inventory for Somatoform Syndromes) questionnaire with 45 or less score points
Medical history of hypersensitivity or intolerance to the investigational product or its ingredients or to ingredients of similar chemical structure, Known history of severe cardiovascular disease, Known history of or acute mental illness such as severe depression, psychosis, bipolar disorder, mania, anxiety, or obsessive-compulsive disorder, Known history of addictive disease (e.g., alcohol, medication, drug addiction), Answered during Screening less than 12 times of 18 the pain intensity (NRS) inquiry, Laboratory liver values: Alanine aminotransferase (ALT, GPT) > 3 x ULN (Upper Limit of Normal range), Aspartate aminotransferase (AST, GOT) > 3 x ULN, Alkaline phosphatase (AP) > 2.5 x ULN, and for bilirubin > 1.5 x ULN, Laboratory renal value: Serum creatinine > 1.5 ULN, Known intolerance to cannabinoids or cannabis products, Participation in another clinical trial within the last four weeks prior to inclusion, Pregnant or nursing women (as excluded by pregnancy testing at visit 1 for women of childbearing potential), Other medical conditions that do not allow the trial subject to appraise the nature, scope, and potential consequences of the clinical trial, Indications that the trial subject is unlikely to comply with the study protocol (e.g., unwillingness to cooperate), Known use of medicinal cannabis products within the last 8 weeks, Active malignant tumor disease, tumor pain, or other dominant severe pain other than that of the study indication, Known history of severe liver or kidney diseases
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method