- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Post-traumatic Stress Disorder (PTSD).
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EudraCT Number: 2021-003154-23 | Sponsor Protocol Number: 1402-0030 | Start Date*: 2022-04-05 | |||||||||||
Sponsor Name:Boehringer Ingelheim AB | |||||||||||||
Full Title: A Phase II, 8-week-treatment, multicenter, randomized, double-blind, placebo-controlled, parallel group trial to evaluate the efficacy, tolerability and safety of orally administered BI 1358894 in ... | |||||||||||||
Medical condition: Post-Traumatic Stress Disorder (PTSD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) PL (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003072-39 | Sponsor Protocol Number: 41223 | Start Date*: 2012-11-27 | |||||||||||
Sponsor Name:Academic Medical Center, University of Amsterdam | |||||||||||||
Full Title: Oxytocin in PTSD: effectiveness as addition to Narrative Exposure Therapy | |||||||||||||
Medical condition: Posttraumatic stress disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001878-29 | Sponsor Protocol Number: 35RC18_8852_PROPRADO | Start Date*: 2021-05-21 | |||||||||||
Sponsor Name:Rennes University Hospital | |||||||||||||
Full Title: The efficacy of traumatic memory modification using a memory reconsolidation procedure under propranolol among adolescents with post-traumatic stress disorder (PROPRADO) | |||||||||||||
Medical condition: post-traumatic stress disorder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004982-41 | Sponsor Protocol Number: 14865A | Start Date*: 2013-11-11 | |||||||||||
Sponsor Name:H. Lundbeck A/S | |||||||||||||
Full Title: Interventional, randomised, double-blind, parallel-group, placebo-controlled, flexible-dose study of brexpiprazole as adjunctive treatment to paroxetine or sertraline in adult patients suffering... | |||||||||||||
Medical condition: Post-traumatic stress disorder (PTSD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Prematurely Ended) IT (Prematurely Ended) FI (Prematurely Ended) SE (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001288-58 | Sponsor Protocol Number: 40122 | Start Date*: 2012-05-21 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting oxytocin after trauma: The effects of intranasal oxytocin administration on emotional and motivational brain processes in PTSD | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006228-19 | Sponsor Protocol Number: PTF3 | Start Date*: 2012-03-21 | |||||||||||
Sponsor Name:Psykiatrisk Center Ballerup | |||||||||||||
Full Title: The treatment of traumatized refugees with Setraline versus Venlafaxine - a randomized trial. | |||||||||||||
Medical condition: Post traumatic stress disorder (PTSD) Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004153-40 | Sponsor Protocol Number: PTF5 | Start Date*: 2016-01-07 | |||||||||||
Sponsor Name:Competence Centre for Transcultural Psychiatry | |||||||||||||
Full Title: TREATMENT OF SLEEP DISTURBANCES IN TRAUMA-AFFECTED REFUGEES – A RANDOMISED CONTROLLED TRIAL | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004177-83 | Sponsor Protocol Number: 37202 | Start Date*: 2011-11-14 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Boosting the oxytocin system in acute trauma: The effectiveness of intranasal oxytocin treatments and stimulation of social support on preventing trauma related psychopathology | |||||||||||||
Medical condition: Posttraumatic Stress Disorder (PTSD) according to criteria in the DSM-IV | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006714-15 | Sponsor Protocol Number: PTF1 | Start Date*: 2009-05-06 | |||||||||||
Sponsor Name:Psykiatrisk Center Gentofte | |||||||||||||
Full Title: The effect of treatment of traumatised refugees with Traume-Focused Cognitive Behavioural Therapy and antidepressants - a randomised controlled clinical trial. | |||||||||||||
Medical condition: Posttraumatic Stress Disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-007068-27 | Sponsor Protocol Number: 0604603 | Start Date*: 2007-03-23 | |||||||||||
Sponsor Name:CHU Toulouse | |||||||||||||
Full Title: Réduction de la reconsolidation du souvenir traumatique par le propranolol : un essai pilote. | |||||||||||||
Medical condition: Troubles du Stress Post-Traumatique (TSPT) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006386-16 | Sponsor Protocol Number: P060226 | Start Date*: 2008-12-05 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: La reviviscence dans l'état de stress post-traumatique : une pathologie du rappel émotionnel ? Application thérapeutique | |||||||||||||
Medical condition: La reviviscence dans l'Etat de Stress Post-Traumatique | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003563-26 | Sponsor Protocol Number: NL74799.018.20 | Start Date*: 2020-10-15 |
Sponsor Name:TNO | ||
Full Title: Reconsolidation: a new intervention for traumatized healthcare workers. | ||
Medical condition: Post-traumatic stress disorder. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000934-16 | Sponsor Protocol Number: Nl.060.44183 | Start Date*: 2020-06-18 |
Sponsor Name:TNO | ||
Full Title: Reconsolidation: a new intervention towards combat-related PTSD. | ||
Medical condition: Post-traumatic stress disorder. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001718-13 | Sponsor Protocol Number: MP18 | Start Date*: 2019-10-18 |
Sponsor Name:MAPS Europe B.V. | ||
Full Title: An Open- Label, Phase 2, Multicenter Feasibility Study if Manualized MDMA-Assisted Psychotherapy with an fMRI sub-study Assessing Changes in Brain Activity in Subjects with Posttraumatic Stress Dis... | ||
Medical condition: post-traumatic stress disorder (PTSD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) CZ (Completed) NO (Completed) DE (Completed) GB (GB - no longer in EU/EEA) ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-005596-39 | Sponsor Protocol Number: MPELONG | Start Date*: 2022-09-07 |
Sponsor Name:MAPS Europe B.V. | ||
Full Title: Long-Term Safety and Persistence of Effectiveness of Manualized MDMA Assisted Therapy for the Treatment of Posttraumatic Stress Disorder | ||
Medical condition: post-traumatic stress disorder (PTSD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005956-39 | Sponsor Protocol Number: RC31/18/0471 | Start Date*: 2021-04-06 | |||||||||||
Sponsor Name:CHU Toulouse | |||||||||||||
Full Title: Treatment of pediatric Post-traumatic Stress Disorder with memory reactivation under the influence of propranolol: A randomized placebo-controlled trial | |||||||||||||
Medical condition: Post-traumatic Stress Disorder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000312-36 | Sponsor Protocol Number: PTSD-FMS | Start Date*: 2021-05-19 | ||||||||||||||||
Sponsor Name:Henri Laborit Hospital | ||||||||||||||||||
Full Title: Impact of Post-Traumatic Stress Disorder Treatment by Reconsolidation Therapy on Fibromyalgia Syndrome | ||||||||||||||||||
Medical condition: Post-Traumatic Stress Disorder and fibromyalgia syndrome | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003891-20 | Sponsor Protocol Number: NL17389.091.07 | Start Date*: 2007-11-27 | |||||||||||
Sponsor Name:GGZ Nijmegen | |||||||||||||
Full Title: Een gerandomiseerde placebo gecontroleerde studie naar de toegevoegde waarde van D-cycloserine aan exposure therapie bij patiënten met een poststraumatische stress stoornis | |||||||||||||
Medical condition: Posttraumatic stress disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018486-37 | Sponsor Protocol Number: dexa2010 | Start Date*: 2010-05-21 |
Sponsor Name:Kris-och Traumacentrum | ||
Full Title: Treatment of exacerbations of post-traumatic stress disorder by short-term dexamethasone, a pilot study. | ||
Medical condition: Posttraumatic stress syndrome F431 | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000030-39 | Sponsor Protocol Number: na | Start Date*: 2008-12-16 |
Sponsor Name:Ministery of Defense, Military Mental Health - Research Centre | ||
Full Title: Prazosin as add-on therapy in the pharmacological treatment of sleep disturbances in post traumatic stress disorder, a placebo-controlled study using polysomnography | ||
Medical condition: posttraumatic stress disorder (PTSD) | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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