WHO ICTRP trial
CHRONDI
CTIS2024-513595-17-00 · EU Clinical Trials Information System · Not Recruiting
Key facts
| Trial ID | CTIS2024-513595-17-00 |
|---|---|
| Public title | CHRONDI |
| Scientific title | Efficacy and tolerability of ODM-111 in chronic pain due to diabetic peripheral neuropathy - 3133004 |
| Primary sponsor | Orion Corporation |
| Registry | EU Clinical Trials Information System |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): No Therapeutic exploratory (Phase II): Yes Therapeutic confirmatory - (Phase III): No Therapeutic use - (Phase IV): No |
| Countries | Australia;New Zealand;Bulgaria;Czechia;Germany;Hungary;Poland |
| Conditions | CHRONIC PAIN DUE TO DIABETIC PERIPHERAL NEUROPATHY MedDRA version: 21.1Level: LLTClassification code: 10067547Term: Diabetic peripheral neuropathic pain Class: 10029205 MedDRA version: 20.1Level: LLTClassification code: 10049475Term… |
| Interventions | Product Name: Para-Tabs 500 mg tabletti, Product Code:PRD593822, Pharmaceutical Form: TABLET, Other descriptive name: , Strength: , Product Name: ODM-111 Placebo, Product Code:N/A, Pharmaceutical Form: N/A, Other descriptive name: N/A… |
| Registration date | May 7, 2024 |
| Target size | 252 |
| Registry page | euclinicaltrials.eu |
At a glance
- No Results available
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: