Efficacy of Non-opioid Drugs in Addition to Opioid Therapy for Cancer Pain Management (NCT07682558) | Clinical Trial Compass
Not Yet RecruitingPhase 3
Efficacy of Non-opioid Drugs in Addition to Opioid Therapy for Cancer Pain Management
Switzerland318 participantsStarted 2026-10
Plain-language summary
The investigators investigate the efficacy of non-opioid analgesics compared to placebo together with opioid therapy for cancer pain management.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Inpatient setting (discharge possible, if patient returns for End of Study Visit)
* Diagnosis of metastatic or locally advanced cancer
* Cancer pain as defined by IASP (International Association for the Study of Pain)
* Cancer pain therapy with opioids indicated for pain management or start thereof at baseline (drug, dose, and route at treating physician's discretion)
* Average daily pain intensity ≥ 3 on NRS (Numeric Rating Scale)
* Ability to swallow oral medication
* Informed Consent as documented by signature
Exclusion Criteria:
* History of allergy or allergy-like symptoms (bronchospasm, urticaria or severe cutaneous adverse reactions (SCARs)) or hypersensitivity to dipyrone (or other pyrazolones or pyrazolidines) or ibuprofen (or other Non-steroidal anti-inflammatory drug incl. acetylsalicylic acid)
* Moderate to severe renal insufficiency (creatinine-eGFR (estimated Glomerular Filtration Rate) \<45 ml/min)
* Severe heart failure (New York Heart Association class III-IV)
* Severe hepatic impairment (liver cirrhosis with ascites) or hepatic porphyria
* History of agranulocytosis induced by dipyrone (or other pyrazolones or pyrazolidines)
* Active gastric and/or duodenal ulcers or bleeding
* History of recurrent gastric and/or duodenal ulcers or gastrointestinal bleeding (≥2 distinct episodes of proven ulceration or bleeding) or increased tendency to bleeding
* Third trimester of pregnancy
* Breastfeeding
* G6PD deficiency
* Inflammatory bowel dis…
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.