- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Emotional security.
Displaying page 1 of 1.
| EudraCT Number: 2015-003042-47 | Sponsor Protocol Number: InsulaTOP | Start Date*: 2015-12-16 | |||||||||||
| Sponsor Name:Centre Hospitalier Henri Laborit | |||||||||||||
| Full Title: Psycho-biological substrates of therapeutic benefit of thermal cure on Generalized Anxiety Disorders | |||||||||||||
| Medical condition: Generalised Anxiety Disorders | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005773-27 | Sponsor Protocol Number: APHP190353 | Start Date*: 2021-03-09 | |||||||||||
| Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
| Full Title: BARIcitinib Cognitive Emotional and Neural signaTuRE BARICENTRE | |||||||||||||
| Medical condition: Patients with rheumatoid arthritis and indication of baricitinib treatment according to a rheumatologist | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-006126-25 | Sponsor Protocol Number: 06 038 | Start Date*: 2007-06-08 |
| Sponsor Name:CNRS: VAN DER REST Michel | ||
| Full Title: Emotional and Social deficits in Asperger syndrome | ||
| Medical condition: We investigate the Asperger Syndrome, it's a pervasive developmental condition related to autism. It manifests in highly individual ways and can have both positive and negative effects on a person.... | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-003824-36 | Sponsor Protocol Number: SATEME-08 | Start Date*: 2005-09-15 |
| Sponsor Name:Fundació Institut Català de Farmacologia | ||
| Full Title: Randomized, double blind, parallel groups, placebo controlled pivotal clinical trial to asses preliminary efficacy and security of a sublingual Cannabis Standardized Extract (Sativex) added to refe... | ||
| Medical condition: Chemotherapy induced nausea and vomiting | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001288-18 | Sponsor Protocol Number: 16-API-01 | Start Date*: 2019-01-08 | |||||||||||
| Sponsor Name:CHU de Nice | |||||||||||||
| Full Title: ASIC channels and migraine disorders - Proof of concept study on the efficacy of Amiloride in prophylaxis of Migraine with Aura - APAM study | |||||||||||||
| Medical condition: Migraine with aura | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001494-23 | Sponsor Protocol Number: RI-B-2021-7300-07 | Start Date*: 2021-06-10 |
| Sponsor Name:Groupe Hospitalier Diaconesses-Croix-Saint-Simon | ||
| Full Title: EFFICACY OF ROUTINE MANAGEMENT BY LOCAL ANAESTHETIC INFILTRATION IN THE TREATMENT OF PUDENDAL NEURALGIA: A RANDOMISED TRIAL AGAINST SALINE | ||
| Medical condition: Patients with pudendal neuralgia who have failed drug treatment | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002769-37 | Sponsor Protocol Number: DR190058 | Start Date*: 2019-11-13 |
| Sponsor Name:CHRU DE TOURS | ||
| Full Title: Cerebrovascular reaction to nitrous oxide in Resistant Depression: Pilot study (PROTO-BRAIN) | ||
| Medical condition: Resistant Depression - Nervous Breakdown | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002569-20 | Sponsor Protocol Number: BIELEFELD-Janssen-PHRCN-2017 | Start Date*: 2018-11-06 | |||||||||||
| Sponsor Name:CHU Dijon Bourgogne | |||||||||||||
| Full Title: A multicenter phase 2 single-arm proof-of-concept trial assessing the efficacy and safety of ustekinumab in association with prednisone, for the treatment of non-infectious severe uveitis (NISU) | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-005555-80 | Sponsor Protocol Number: V00400SB302 | Start Date*: 2015-05-21 | |||||||||||
| Sponsor Name:Pierre Fabre Dermatologie represented by IRPF | |||||||||||||
| Full Title: Efficacy and safety of Hemangiol solution in the treatment of high risk infantile hemangioma. A Multinational Single Arm Study | |||||||||||||
| Medical condition: High risk infantile haemangioma | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002886-21 | Sponsor Protocol Number: UC-0110/1809 | Start Date*: 2018-12-11 |
| Sponsor Name:UNICANCER | ||
| Full Title: A Phase III randomized study evaluating gemcitabine and paclitaxel versus gemcitabine alone after FOLFIRINOX failure or intolerance in Metastatic Pancreatic Ductal Adenocarcinoma. | ||
| Medical condition: Metastatic Pancreatic Ductal Adenocarcinoma | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-002889-41 | Sponsor Protocol Number: UC-BCG-2103 | Start Date*: 2022-04-29 | ||||||||||||||||
| Sponsor Name:UNICANCER | ||||||||||||||||||
| Full Title: LESS: Single-arm study to de-escalate adjuvant endocrine therapy duration in women with HR+ HER2- breast cancer at very low risk of metastasis | ||||||||||||||||||
| Medical condition: Post-menopausal women with localized luminal A breast cancer and considered at low risk of metastatic relapse | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-004027-52 | Sponsor Protocol Number: GINECO-OV125b | Start Date*: 2015-11-30 | ||||||||||||||||
| Sponsor Name:ARCAGY Research | ||||||||||||||||||
| Full Title: Randomized, Double-Blind, Phase III Trial of Olaparib vs. Placebo in Patients with Advanced FIGO Stage IIIB – IV High Grade Serous or Endometrioid Ovarian, Fallopian Tube, or Peritoneal Cancer trea... | ||||||||||||||||||
| Medical condition: Patients with advanced FIGO stage IIIB – IV high grade epithelial ovarian, fallopian tube, or peritoneal cancer treated with standard first-line treatment | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DE (Ongoing) AT (Completed) BE (Completed) ES (Ongoing) DK (Completed) SE (Completed) FI (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-003468-38 | Sponsor Protocol Number: OLA-TMZ-RTE-01 | Start Date*: 2017-03-17 | |||||||||||
| Sponsor Name:Centre François baclesse | |||||||||||||
| Full Title: Phase I/IIa study of concomitant radiotherapy with olaparib and temozolomide in unresectable high grade gliomas patients | |||||||||||||
| Medical condition: First line treatment of patients with unresectable high-grade gliomas | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-003392-32 | Sponsor Protocol Number: 2014/VCC/0014 | Start Date*: 2014-10-24 | |||||||||||
| Sponsor Name:Velindre NHS Trust | |||||||||||||
| Full Title: A Phase II/III trial of risk-stratified, reduced intensity adjuvant treatment in patients undergoing transoral surgery for Human papillomavirus (HPV)-positive oropharyngeal cancer | |||||||||||||
| Medical condition: Oropharyngeal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) DE (Trial now transitioned) ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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