- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Cold pressor test.
Displaying page 1 of 1.
| EudraCT Number: 2018-003939-30 | Sponsor Protocol Number: 2018-0910-4 | Start Date*: 2019-02-08 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: Determination of analgesic equipotent doses of inhaled metoxyflurane vs. intravenous fentanyl using cold pressor test (CPT) in volunteers: A randomized, double blind, placebo-controlled crossover s... | ||
| Medical condition: Experimental pain model (cold pressor test – CPT) will be used to determinate equipotent doses of inhaled metoxyflurane vs. intravenous fentanyl. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-004470-10 | Sponsor Protocol Number: AKF-372 | Start Date*: 2008-01-28 |
| Sponsor Name:Institut for Sundhedstjenesteforskning, Klinisk Farmakologi, Syddansk Universitet | ||
| Full Title: "Effekten af escitalopram på tramdadols farmakokinetik og farmakodynamik" | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004082-42 | Sponsor Protocol Number: OXY-2 | Start Date*: 2005-12-05 |
| Sponsor Name:Søren Sindrup, Dept. of Neurology, University Hospital of Odense | ||
| Full Title: The Pharmacogenetics of Oxycodone analgesia in human experimental pain models | ||
| Medical condition: Healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002302-43 | Sponsor Protocol Number: CHDR1209 | Start Date*: 2012-06-08 | ||||||||||||||||
| Sponsor Name:Dr. Reddy's Laboratories Ltd. | ||||||||||||||||||
| Full Title: A study to investigate the analgesic effects of buprenorphine and milnacipram in healthy volunteers. | ||||||||||||||||||
| Medical condition: Pain therapeutics, neuropathic pain, nociceptive pain, synergism between opioids and TCA. | ||||||||||||||||||
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| Population Age: Adults | Gender: Male | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2012-002871-32 | Sponsor Protocol Number: Rifabupre | Start Date*: 2012-08-28 |
| Sponsor Name:Turku University hospital | ||
| Full Title: Effects of rifampicin on the pharmacokinetics and pharmacodynamics of sublingual and intravenous buprenorphine: A four-phase cross-over study in healthy subjects. | ||
| Medical condition: Healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000298-35 | Sponsor Protocol Number: NL60593.028.17 | Start Date*: 2017-05-01 |
| Sponsor Name:Tilburg University | ||
| Full Title: Oxytocin, friendship and dealing with emotions | ||
| Medical condition: There are no medical conditions or disease under investigation. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005086-20 | Sponsor Protocol Number: CHDR1117 | Start Date*: 2011-11-22 |
| Sponsor Name:Centre for Human Drug Research (CHDR) | ||
| Full Title: Effects of paracetamol on nociception in adolescents. | ||
| Medical condition: Nociceptive pain (disorders) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-006334-39 | Sponsor Protocol Number: CP130-1016 | Start Date*: 2022-01-10 | |||||||||||
| Sponsor Name:Trevena Inc | |||||||||||||
| Full Title: Protocol title should be: A randomised, double-blind, placebo-controlled, dose-ranging partial-block crossover study to investigate the effect of intravenous oliceridine on CNS functioning and noc... | |||||||||||||
| Medical condition: Acute Pain | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-002976-14 | Sponsor Protocol Number: CRI103143 | Start Date*: 2006-09-27 |
| Sponsor Name:GlaxoSmithKline Research and Development Limited | ||
| Full Title: A phase IIa, single-centre, randomised, placebo-controlled, double-blind, three-period crossover exploratory study investigating the effects on gut autonomic responses of single administrations of ... | ||
| Medical condition: Irritable Bowel Syndrome (IBS) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003208-22 | Sponsor Protocol Number: CaPsaPPP-01 | Start Date*: 2015-11-06 |
| Sponsor Name:Wilhelminen hospital | ||
| Full Title: Does a two-day pretreatment with capsaicin reduce postoperative hyperalgesia and pain in surgical patients A prospective, randomized, double-blind, placebo-controlled, parallel group, single-cente... | ||
| Medical condition: postoperative secondary mechanical hyperalgesia and postoperative pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-002909-10 | Sponsor Protocol Number: P137 | Start Date*: 2022-10-24 |
| Sponsor Name:Maastricht University | ||
| Full Title: THE IMPACT OF PSILOCYBIN ON PAIN IN FIBROMYALGIA PATIENTS AND HEALTHY VOLUNTEERS: A MULTICENTER TRIAL | ||
| Medical condition: Fibromyalgia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-005506-32 | Sponsor Protocol Number: Dulo2006 | Start Date*: 2007-03-05 | |||||||||||
| Sponsor Name:Danish Pain Research Center | |||||||||||||
| Full Title: Pain, anxiety and depression in neuropathic and non-neuropathic pain: Effect of monoamine modulation. | |||||||||||||
| Medical condition: Chronic pain: neuropathic pain and fibromyalgia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004375-12 | Sponsor Protocol Number: TODINELI | Start Date*: 2014-02-13 | |||||||||||||||||||||
| Sponsor Name:Center of Mech-Sense | |||||||||||||||||||||||
| Full Title: TODINELI Trial A randomized, double-blinded, single-centre, parallel-group, placebo-controlled, prospective trial of the neuroprotective effect of Liraglutide for treatment of diabetic neuropathy | |||||||||||||||||||||||
| Medical condition: TODINELI Trial A randomized, double-blinded, single-centre, parallel-group, placebo-controlled, prospective trial of the neuroprotective effect of Liraglutide for treatment of diabetic neuropathy i... | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
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