- Trials with a EudraCT protocol (9)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9 result(s) found for: Cravings.
Displaying page 1 of 1.
EudraCT Number: 2008-005363-34 | Sponsor Protocol Number: EC/2008/50/FAHS | Start Date*: 2009-03-10 | |||||||||||
Sponsor Name:University of Surrey | |||||||||||||
Full Title: Investigation to explore whether there is a synergistic effect between nicotine replacement therapy and guided bodyscanning on cigarette cravings and withdrawal symptoms in temporarily abstinent sm... | |||||||||||||
Medical condition: Healthy volunteers who currently smoke 10 or more cigarettes per day, for the last 3 years. The trial intends to explore whether there is a synergistic effect between the relaxation technique of g... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004516-22 | Sponsor Protocol Number: 04-4025 | Start Date*: 2005-02-01 |
Sponsor Name:Uppsala University | ||
Full Title: The impact of steroid hormones on symptom provocation in patients with premenstrual dysphoric disorder. | ||
Medical condition: Premenstrual Dysphoric Disorder | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
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: 2015-004463-37 | Sponsor Protocol Number: 140682 | Start Date*: 2016-06-20 |
Sponsor Name:St. Olavs Hospital | ||
Full Title: ACUTE AND LONG-TERM EFFECTS OF INTRANASAL OXYTOCIN IN ALCOHOL WITHDRAWAL AND DEPENDENCE: A PROSPECTIVE RANDOMIZED PARALLEL GROUP PLACEBO-CONTROLLED TRIAL | ||
Medical condition: alcohol withdrawal and craving. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-002280-10 | Sponsor Protocol Number: LBS180319 | Start Date*: 2021-04-14 | |||||||||||
Sponsor Name:St. Olav's University Hospital | |||||||||||||
Full Title: Effects of intranasal oxytocin in the treatment of benzodiazepine withdrawal: A pilot randomized parallel group placebo-controlled trial | |||||||||||||
Medical condition: Benzodiazepine withdrawal and craving | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||
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: 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: 2014-002708-26 | Sponsor Protocol Number: CRC341 | Start Date*: 2017-06-28 | ||||||||||||||||
Sponsor Name:University of Surrey | ||||||||||||||||||
Full Title: A randomised double blind placebo controlled pilot trial of oxytocin efficacy in treating detoxified opioid dependent individuals | ||||||||||||||||||
Medical condition: Opioid dependence. The study will be investigating the efficacy of Syntocinon (oxytocin) on treating the withdrawal symptoms and cravings that opioid (e.g. almost always heroin) dependent individua... | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
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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