- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
80 result(s) found for: Physical dependence.
Displaying page 1 of 4.
EudraCT Number: 2007-002315-92 | Sponsor Protocol Number: 12013A | Start Date*: 2008-11-12 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: A 52-week, randomised, double-blind, placebo-controlled, parallel-group, safety, tolerability and efficacy study of nalmefene, as needed use, in patients with alcohol dependence | |||||||||||||
Medical condition: Alcohol dependence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SK (Completed) EE (Completed) GB (Completed) LV (Completed) HU (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002462-32 | Sponsor Protocol Number: SHW01 | Start Date*: 2022-12-09 | |||||||||||
Sponsor Name:Suchthilfe Wien gGmbH | |||||||||||||
Full Title: Pilot study on the safety and feasibility of intravenous opioid agonist therapy (OAT) with Hydagelan® (hydromorphone hydrochloride) in Vienna. | |||||||||||||
Medical condition: Opioid dependence: Opioid dependence is a serious and usually chronic disease that requires treatment, encompasses various psychological and physical dimensions, and is associated with concomitant ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004024-11 | Sponsor Protocol Number: 60-60600-97-103 | Start Date*: 2014-07-23 | |||||||||||
Sponsor Name:Academic Psychiatric Center - AMC-UvA | |||||||||||||
Full Title: New pharmacotherapeutic treatment options for crack-cocaine dependent people in the Netherlands: A double-blind, placebo-controlled randomized feasibility study of sustained release dexamphetamine | |||||||||||||
Medical condition: cocaine dependence (according DSM-IV) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000736-33 | Sponsor Protocol Number: CAFQ056X2201 | Start Date*: 2017-10-25 | |||||||||||
Sponsor Name:Novartis Farmacéutica S.A. | |||||||||||||
Full Title: A randomized, subject and investigator blinded, placebo-controlled, parallel group study to investigate whether AFQ056 reduces cocaine use in patients diagnosed with Cocaine Use Disorder (CUD). | |||||||||||||
Medical condition: Cocaine Use Disorder according to DSM 5 | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001154-98 | Sponsor Protocol Number: 15660A | Start Date*: 2013-10-14 | |||||||||||
Sponsor Name:H Lundbeck A/S [...] | |||||||||||||
Full Title: Interventional, randomized, double-blind, cross-over, placebo-controlled study to investigate the effects of nalmefene after single dose on the blood oxygen level dependent (BOLD) fMRI signal in th... | |||||||||||||
Medical condition: Nalmefene (Selincro) is indicated for the reduction of alcohol consumption in adults with alcohol dependence who have a high drinking risk level, without physical withdrawal symptoms and who do not... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000069-57 | Sponsor Protocol Number: P15-01 | Start Date*: 2017-07-21 | |||||||||||
Sponsor Name:BIOPROJET PHARMA | |||||||||||||
Full Title: A Multisite Randomized Clinical Trial Evaluating BP1.3656 Versus Placebo For Alcohol Use Disorder Treatment | |||||||||||||
Medical condition: Male or female with moderate or severe DSM-5 alcohol use disorder (based on the alcohol use disorders section of MINI) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002229-23 | Sponsor Protocol Number: RB-UK-11-0018 | Start Date*: 2012-05-09 | |||||||||||
Sponsor Name:RB Pharmaceuticals Inc. | |||||||||||||
Full Title: A randomised, double blind, placebo controlled, cross over study of the effects of Buprenorphine Hemiadipate Hydrochloride/Naloxone Hydrochloride Dihydrate intravenous challenges in opioid dependen... | |||||||||||||
Medical condition: Maintenance/substitution agent for the treatment of opioid dependence. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003250-29 | Sponsor Protocol Number: IPAB-07-002 | Start Date*: 2008-03-14 | |||||||||||
Sponsor Name:Independent Pharmaceutica AB | |||||||||||||
Full Title: A randomised, placebo-controlled, multi-centre study on the efficacy of Niccine, a vaccine for nicotine, in smoking relapse prevention, assessed in abstinent, adult smokers. | |||||||||||||
Medical condition: The intended indication for the drug under investigation is smoking relapse prevention. Tobacco smoking has been identified as the single largest preventable cause of morbidity and premature death ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002374-55 | Sponsor Protocol Number: S3250493 | Start Date*: 2007-08-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: Simultaneous fMRI/EEG of the 4 mg nicotine lozenge in relief of cognitive impairment associated with nicotine withdrawal | |||||||||||||
Medical condition: Nicotine dependence | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003035-35 | Sponsor Protocol Number: HS-14-499 | Start Date*: 2015-11-09 |
Sponsor Name:Braeburn Pharmaceuticals | ||
Full Title: An Open-Label Multicenter Study Assessing the Long-Term Safety of a Once-Weekly and Once-Monthly, Long-Acting Subcutaneous Injection Depot of Buprenorphine (CAM2038) in Adult Outpatients with Opioi... | ||
Medical condition: Opioid Use Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Completed) DK (Completed) HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021384-33 | Sponsor Protocol Number: NTXMR1 | Start Date*: 2010-08-20 |
Sponsor Name:Beroendecentrum Stockholm | ||
Full Title: The Effect of Naltrexone on Amphetamine Cue Reactivity: An fMRI Study | ||
Medical condition: Amphetamine dependence | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002203-40 | Sponsor Protocol Number: 07.0056 | Start Date*: 2007-10-03 | |||||||||||
Sponsor Name:St. George's, University of London | |||||||||||||
Full Title: Effect of hydrocortisone on desire to smoke and tobacco withdrawal symptoms | |||||||||||||
Medical condition: Nicotine addiction; specifically, cortisol deficiency following smoking cessation. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010584-16 | Sponsor Protocol Number: 2009/001 | Start Date*: 2010-10-25 | |||||||||||||||||||||
Sponsor Name:ZonMw | |||||||||||||||||||||||
Full Title: New pharmacotherapeutic treatment options for crack-cocaine dependent people in the Netherlands. | |||||||||||||||||||||||
Medical condition: Crack-cocaine dependence (according to DSM-IV) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004692-36 | Sponsor Protocol Number: VAR/01/011 | Start Date*: 2011-11-30 | ||||||||||||||||
Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE | ||||||||||||||||||
Full Title: COMBIVAR. Randomized double-blind trial of two parallel groups design to evaluate the efficacy of smoking cessation with combined (varenicline plus nicotine patches) versus monotherapy (varenicline) | ||||||||||||||||||
Medical condition: NICOTINE DEPENDENCE. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005938-15 | Sponsor Protocol Number: CloTASH-2021-2Version15.10.21 | Start Date*: 2021-11-03 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Health risks and treatment of anabolic-androgenic steroid (AAS) induced hypogonadism among men – a pilot study exploring off-label use of clomiphene citrate to reduce symptoms of androgen deficienc... | ||
Medical condition: Anabolic androgenic steroid induced hypogonadism among men | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017862-22 | Sponsor Protocol Number: 200110005 | Start Date*: 2010-09-28 | |||||||||||
Sponsor Name:ZonMw | |||||||||||||
Full Title: The effectiveness of Nicotine Replacement Therapy for young people aged 12 to 18 years | |||||||||||||
Medical condition: Smoking among young people aged 12 – 18 years. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004211-40 | Sponsor Protocol Number: MTI-107 | Start Date*: 2018-06-07 | |||||||||||
Sponsor Name:Menlo Therapeutics Inc. | |||||||||||||
Full Title: An Open-Label Long-Term Safety Study of Serlopitant for the Treatment of Pruritus | |||||||||||||
Medical condition: Pruritus associated with prurigo nodularis (PN), atopic dermatitis (AD), or psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000575-14 | Sponsor Protocol Number: SMO032/10/03 | Start Date*: 2012-05-09 | |||||||||||
Sponsor Name:D&A PHARMA | |||||||||||||
Full Title: Randomized, multicenter, double-blind, placebo-controlled study of the safety and efficacy of 4 dose regimens of SMO.IR, an oral solid formulation of sodium oxybate, in the maintenance of alcohol a... | |||||||||||||
Medical condition: maintenance of alcohol abstinence in recently abstinent alcohol-dependent patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) AT (Completed) IT (Completed) SK (Completed) DE (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006741-40 | Sponsor Protocol Number: CNIC002A2201 | Start Date*: 2008-07-14 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A double blind, placebo-controlled, multi-centre study to evaluate the efficacy, safety, tolerability and immunogenicity of repeated s.c administrations of 100µg NIC002 vaccine in cigarette smokers... | ||
Medical condition: Smokers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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) |
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