- Trials with a EudraCT protocol (10)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
10 result(s) found for: LTP.
Displaying page 1 of 1.
| 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: 2014-001541-24 | Sponsor Protocol Number: NeuroIPT-1 | Start Date*: 2016-03-07 |
| Sponsor Name:University Medical Center Freiburg | ||
| Full Title: Neuroenhancement of Interpersonal Psychotherapy in Major Depression | ||
| Medical condition: Major Depression (ICD-10; F32.2/F33.2) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-005038-53 | Sponsor Protocol Number: FIM-PRU-2018-01 | Start Date*: 2019-05-16 | |||||||||||
| Sponsor Name:Fundación Pública Andaluza para la Investigación de Málaga en Biomedicina Y Salud (FIMABIS) | |||||||||||||
| Full Title: Randomized double-blind, placebo-controlled study evaluate the efficacy and mechanisms involved in immunotherapy Sublingual specifies with Pru p 3 (Pru p 3-ITSL) in patients with allergy to nsLTP w... | |||||||||||||
| Medical condition: LTP syndrome. | |||||||||||||
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| Population Age: Children, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003405-26 | Sponsor Protocol Number: NF1-EXCEL | Start Date*: 2014-09-03 | |||||||||||
| Sponsor Name:Erasmus MC | |||||||||||||
| Full Title: The effect of Lamotrigine on cognitive deficits associated with Neurofibromatosis type 1: a phase II randomized controlled multi-centre trial (NF1-EXCEL) | |||||||||||||
| Medical condition: Neurofibromatosis type 1 | |||||||||||||
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| Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) BE (Completed) DK (Prematurely Ended) ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-003943-20 | Sponsor Protocol Number: DX-2930-03 | Start Date*: 2016-03-31 | |||||||||||
| Sponsor Name:Dyax Corp., an indirect, wholly-owned subsidiary of Shire plc. | |||||||||||||
| Full Title: HELP Study™: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Efficacy and Safety Study to Evaluate DX 2930 For Long-Term Prophylaxis Against Acute Attacks of Hereditary Angioedema (HAE) | |||||||||||||
| Medical condition: Hereditary angioedema (HAE) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-005255-27 | Sponsor Protocol Number: DX-2930-04 | Start Date*: 2016-11-30 | |||||||||||
| Sponsor Name:Dyax Corp. (an indirect, wholly-owned subsidiary of Shire plc.) | |||||||||||||
| Full Title: HELP Study ExtensionTM: An Open-Label Study to Evaluate the Long-Term Safety and Efficacy of DX-2930 for Prevention Against Acute Attacks of Hereditary Angioedema (HAE) | |||||||||||||
| Medical condition: Type I and Type II Hareditary Angioedema (HAE) | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2023-001105-31 | Sponsor Protocol Number: SHP643-304 | Start Date*: 2024-04-26 |
| Sponsor Name:Takeda | ||
| Full Title: A Multi-center, Open-label Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of Lanadelumab (SHP643) in Chinese Subjects with Hereditary Angioedema | ||
| Medical condition: Hereditary Angioedema (HAE) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2017-002239-41 | Sponsor Protocol Number: SC17.01 | Start Date*: 2018-02-16 | |||||||||||
| Sponsor Name:I.R.C.C.S. FONDAZIONE S.LUCIA | |||||||||||||
| Full Title: Effects of Safinamide therapy on reuroplasticity in patients with Parkinson's disease | |||||||||||||
| Medical condition: Parkinson's disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002895-42 | Sponsor Protocol Number: GITS2013_4.0 | Start Date*: 2013-10-10 | ||||||||||||||||
| Sponsor Name:Region Västerbotten | ||||||||||||||||||
| Full Title: Glaucoma Intensity Treatment Study – Intensive non-invasive glaucoma treatment vs conventional stepwise treatment – a prospective, randomized phase IV study of disease progression in glaucoma (GITS... | ||||||||||||||||||
| Medical condition: Glaucoma, open-angle and PEX glaucoma. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-002369-14 | Sponsor Protocol Number: CHUB-Psy-PAThforsAUD | Start Date*: 2023-07-20 | |||||||||||
| Sponsor Name:CHU Brugmann | |||||||||||||
| Full Title: Psilocybin-Assisted Therapy for Severe Alcohol Use Disorder: Feasibility, Clinical Efficacy & (Neuro)cognitive Mechanisms. | |||||||||||||
| Medical condition: Severe Alcohol Use Disorder | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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