- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (190)
8 result(s) found for: Opium.
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EudraCT Number: 2020-000396-20 | Sponsor Protocol Number: Dropizol_2020 | Start Date*: 2021-01-02 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: Opium tincture against chronic diarrhea - Patients: An investigator initiated, randomized placebo-controlled, clinical trial | |||||||||||||
Medical condition: Chronic diarrhea | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004875-41 | Sponsor Protocol Number: Dropizol_healthy_2020 | Start Date*: 2021-01-02 | |||||||||||
Sponsor Name:Mech-Sense, Aalborg University Hospital | |||||||||||||
Full Title: Opium tincture against chronic diarrhea - Healthy: An investigator initiated, randomized placebo-controlled, double-blinded, cross-over, clinical trial | |||||||||||||
Medical condition: Chronic diarrhea - The effect of opium tincture on the gastrointestinal function | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021814-43 | Sponsor Protocol Number: 5703433 | Start Date*: 2011-05-17 | |||||||||||
Sponsor Name:Ulrich Tacke | |||||||||||||
Full Title: The Safety and Tolerability of Methadone/Naloxone Combination in Opioid Substitution Treatment | |||||||||||||
Medical condition: Patients with opioid addiction. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002948-28 | Sponsor Protocol Number: Loop | Start Date*: 2006-10-26 | |||||||||||
Sponsor Name:MAROS Arzneimittel GmbH | |||||||||||||
Full Title: Prospective randomized monoinstitutional study of the treatment of therapy-associated diarrhea during percutaneous radiation therapy of the small pelvis. – Comparison of loperamide and tincture of ... | |||||||||||||
Medical condition: Therapy-associated diarrhea during radiaton therapy of small pelvis (including enteritis as a result of radiation therapy and enteritis as a result of radiation- and chemotherapy). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007877-22 | Sponsor Protocol Number: 2007IC013H | Start Date*: 2008-07-10 | |||||||||||
Sponsor Name:Royal Brompton & Harefield NHS Trust | |||||||||||||
Full Title: A prospective blinded randomised placebo controlled trial investigating whether oxycodone modified release reduces parenteral opioid use following intermediate thoracic surgery | |||||||||||||
Medical condition: The management of acute pain after intermediate thoracic surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004735-68 | Sponsor Protocol Number: AOUC-001-2013 | Start Date*: 2014-05-27 | |||||||||||
Sponsor Name:Azienda Ospedaliero Universitaria Careggi, Firenze | |||||||||||||
Full Title: Short-Term Effect of Levodropropizine on Respiratory Centre Output in Normal Subjects and Patients with Intractable Chronic Cough | |||||||||||||
Medical condition: Patients with chronic cough | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: 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 (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019066-92 | Sponsor Protocol Number: 2-55-52030-730/TR321 | Start Date*: 2010-08-31 | |||||||||||
Sponsor Name:Ipsen Pharma SAS | |||||||||||||
Full Title: A double-blind, randomized placebo-controlled clinical trial investigating the efficacy and safety of Somatuline Depot (lanreotide) Injection in the treatment of carcinoid syndrome | |||||||||||||
Medical condition: Carcinoid syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) LV (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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