- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Drug Overdose.
Displaying page 1 of 1.
EudraCT Number: 2017-000246-21 | Sponsor Protocol Number: PP100-001 | Start Date*: 2017-04-25 | |||||||||||
Sponsor Name:PledPharma AB | |||||||||||||
Full Title: A Randomised Open Label Exploratory, Safety and Tolerability Study with PP100-01 in Patients Treated with the 12-hour Regimen of N-Acetylcysteine for Paracetamol/Acetaminophen Overdose | |||||||||||||
Medical condition: The objective of this study is to develop a therapeutic regimen for paracetamol/acetaminophen overdose (POD) where a novel NAC 12hr regime is combined with a superoxide dismutase (SOD) mimetic, PP1... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017800-10 | Sponsor Protocol Number: CZB/4/722 | Start Date*: 2010-04-01 | ||||||||||||||||
Sponsor Name:NHS Lothian [...] | ||||||||||||||||||
Full Title: Scottish and Newcastle Anti-emetic Pre-treatment for Paracetamol Poisoning study (SNAP) | ||||||||||||||||||
Medical condition: Paracetamol overdose | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001877-34 | Sponsor Protocol Number: HOT-Treated | Start Date*: 2016-11-25 | |||||||||||||||||||||
Sponsor Name:South London and Maudsley NHS Foundation Trust [...] | |||||||||||||||||||||||
Full Title: Improving understanding of Heroin Overdose Testing: diamorphine dose-escalation testing in a treated population | |||||||||||||||||||||||
Medical condition: Opioid Overdose | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004072-22 | Sponsor Protocol Number: NINA-1 | Start Date*: 2017-12-07 | |||||||||||||||||||||||||||||||
Sponsor Name:Norwegian University of Science and Technology (NTNU) | |||||||||||||||||||||||||||||||||
Full Title: NTNU Intranasal Naloxone Trial Double blinded, double dummy, randomised controlled trial of intranasal naloxone for pre hospital use | |||||||||||||||||||||||||||||||||
Medical condition: We investigate the reversal of opioid overdoses in the pre hospital setting | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NO (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-015647-16 | Sponsor Protocol Number: ANV-09-008 | Start Date*: 2010-01-28 | |||||||||||
Sponsor Name:GUIDE Clinic, St James's Hospital | |||||||||||||
Full Title: The pharmacokinetics of once daily Kaletra and methadone in a population of HIV positiive drug users. | |||||||||||||
Medical condition: HIV-1 Positive Injection Drug Users | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002073-26 | Sponsor Protocol Number: 1125-ECIR | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Medical Center - University of Freiburg | |||||||||||||||||||||||
Full Title: Phase 1/2 Trial to determine the safety and efficacy of Extracorporeal photopheresis as treatment for steroid-refractory immune related adverse events after immune checkpoint inhibitor therapy | |||||||||||||||||||||||
Medical condition: Immune related adverse events induced by treatment with immune checkpoint inhibitors (monoclocanl antibodies against PD-1, PD-L1 or CTLA-4) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000305-24 | Sponsor Protocol Number: AN01AC11 | Start Date*: 2021-03-18 |
Sponsor Name:Anebulo pharmaceuticals, Inc. | ||
Full Title: A randomized, double-blind, placebo-controlled study to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of single oral doses of CB1 antagonist ANEB-001 in healthy occasional ... | ||
Medical condition: THC intoxication | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002544-40 | Sponsor Protocol Number: 5866 | Start Date*: 2014-10-29 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: THE TREATMENT OF HYPERTENSION ASSOCIATED WITH SEVERE PREECLAMPSIA. A RANDOMIZED CONTROLLED TRIAL OF URAPIDIL VERSUS NICARDIPINE. The URANIC trial. | ||
Medical condition: Hypertension associated with severe pre eclampsia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005192-89 | Sponsor Protocol Number: C1231001 | Start Date*: 2015-04-21 | |||||||||||
Sponsor Name:Hospira UK Ltd. | |||||||||||||
Full Title: Post-Marketing Observational Cohort Study of Patients with Inflammatory Bowel Disease (IBD) Treated with CT-P13 in Usual Clinical Practice (CONNECT-IBD) | |||||||||||||
Medical condition: Inflamatory Bowel Disease (IBD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000641-44 | Sponsor Protocol Number: TailorDose-II | Start Date*: 2017-04-28 | |||||||||||
Sponsor Name:Karolinska intitutet | |||||||||||||
Full Title: TailorDose®-II: Therapeutic dose monitoring of commonly used cytostatic drugs/regimes indicated for breast cancer | |||||||||||||
Medical condition: Newly diagnosed pre- or post-operative breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000439-14 | Sponsor Protocol Number: CMBG453C12201 | Start Date*: 2021-03-17 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A phase II multi-center, single arm, safety and efficacy study of MBG453 in combination with azacitidine and venetoclax for the treatment of Acute Myeloid Leukemia (AML) in adult patients unfit for... | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) in adult patients unfit for chemotherapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001997-70 | Sponsor Protocol Number: EXCELLENCE/0421/0543v1 | Start Date*: 2022-11-16 | ||||||||||||||||||||||||||
Sponsor Name:University of Cyprus | ||||||||||||||||||||||||||||
Full Title: Efficacy of Ketamine for the Prevention of Relapse in Patients with Opioid-Use Disorders (OUD) | ||||||||||||||||||||||||||||
Medical condition: Methadone and buprenorphine comprise a first-line, evidence-based opioid substitution treatment (OST) for OUD patients. Unfortunately, retention and adherence to OST treatment is currently a major ... | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CY (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002869-18 | Sponsor Protocol Number: | Start Date*: 2019-09-04 | |||||||||||
Sponsor Name:Cumbria, Northumberland, Tyne and Wear NHS Foundation Trust | |||||||||||||
Full Title: A randomised, double-blind, placebo controlled trial of pramipexole in addition to mood stabilisers for patients with treatment resistant bipolar depression. | |||||||||||||
Medical condition: Bipolar disorder (BD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
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