- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
101 result(s) found for: BOLD.
Displaying page 1 of 6.
EudraCT Number: 2018-001212-30 | Sponsor Protocol Number: ECEP-BPD | Start Date*: 2018-09-18 | |||||||||||
Sponsor Name:Central Institute of Mental Health, represented by commercial and administrative Director | |||||||||||||
Full Title: A trial to study effects of a single dose Citalopram on emotion processing in female patients with Borderline Personality Disorder and the associated modulation of fMRI BOLD signals | |||||||||||||
Medical condition: Borderline Personality Disorder | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001839-23 | Sponsor Protocol Number: 14137A | Start Date*: 2012-05-14 |
Sponsor Name:H. Lundbeck A/S | ||
Full Title: Interventional randomised, double-blind, parallel-group, placebo-controlled, exploratory study investigating the effects of Lu AA21004 on cognition and BOLD fMRI signals in subjects remitted fro... | ||
Medical condition: Cognitive dysfunction Major depressive disorder (MDD) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004762-23 | Sponsor Protocol Number: P/2014/237 | Start Date*: 2015-03-26 |
Sponsor Name:CHRU Besançon | ||
Full Title: NO | ||
Medical condition: sujets à l'attachement insécure | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-015538-30 | Sponsor Protocol Number: OXTsozphob | Start Date*: 2010-04-21 | |||||||||||
Sponsor Name:Rheinisch-Westfälisch Technische Hochschule Aachen | |||||||||||||
Full Title: Effect of intranasal oxytocin on social approach in patients with social phobia and healthy control | |||||||||||||
Medical condition: The effect of oxytocin is investigated in social processing of social phobic patient and healthy controls | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000908-15 | Sponsor Protocol Number: IMI2-PainCare-BioPain-RCT4 | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name:Aarhus University | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, cross-over trial in healthy subjects to investigate the effects of lacosamide, pregabalin and tapentadol on biomarkers of pain processing observed by... | |||||||||||||
Medical condition: Healthy volunteers (intended indication: pain) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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: 2007-005353-28 | Sponsor Protocol Number: A3360529 | Start Date*: 2009-11-02 |
Sponsor Name:GlaxoSmithKline, S.A. | ||
Full Title: A randomised, double-blind, evaluation of the effects of paracetamol on the BOLD fMRI response to painful stimuli in subjects with osteoarthritis. Estudio doble-ciego, aleatorizado para evaluar lo... | ||
Medical condition: Este es un estudio metodológico diseñado para investigar la sensibilidad de la técnica de resonancia magnetica funcional para detectar los efectos de un día de tratamiento con paracetamol de libera... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-005518-16 | Sponsor Protocol Number: U3P | Start Date*: 2021-05-10 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: U3P study - Upadacitinib in Psoriatic Arthritis Pain Processing | |||||||||||||
Medical condition: Psoriatic arthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001772-22 | Sponsor Protocol Number: 96HCL15_0122 | Start Date*: 2016-01-25 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Mesures des modifications hémodynamiques, fonctionnelles et métaboliques rénales par TEP et BOLD- IRM en lien avec la modification des apports en AGE dans l’alimentation, ou avec sevelamer. ETUDE A... | |||||||||||||
Medical condition: Volontaires sains | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002604-12 | Sponsor Protocol Number: PSY-NIL-0010 | Start Date*: 2022-02-09 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Unraveling the aesthetic mind in anhedonia, insights from pharmacological imaging of the human brain: A single-blind, randomized, placebo-controlled cross-over study | ||
Medical condition: Depression | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000377-12 | Sponsor Protocol Number: CHUBX2014/26 | Start Date*: 2017-09-18 | ||||||||||||||||
Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
Full Title: MISOBOLD - Prostate cancer hypoxia using BOLD MRI and 18F-FMISO PET imaging | ||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003079-41 | Sponsor Protocol Number: BOLD-100-001 | Start Date*: 2023-01-06 | ||||||||||||||||||||||||||
Sponsor Name:Bold Therapeutics, Inc. (Bold) | ||||||||||||||||||||||||||||
Full Title: A Phase 1b/2a Dose Escalation Study of BOLD-100 in Combination with FOLFOX Chemotherapy in Patients with Advanced Solid Tumours | ||||||||||||||||||||||||||||
Medical condition: Colorectal Cancer Pancreatic Cancer Gastric Cancers Cholangiocarcinoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: IE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005630-21 | Sponsor Protocol Number: RG_06-180 | Start Date*: 2009-04-09 |
Sponsor Name:University of Birmingham
[...]
1. University of Birmingham
2. Birmingham Heartlands Hospital |
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Full Title: The effect of Pregabalin on Pain progressing in Painful Diabetic Neuropathy | ||
Medical condition: Diabtes and its complications, painful neuropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-015584-13 | Sponsor Protocol Number: 1A-AGE/ONSET | Start Date*: 2009-10-20 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Onset-tid samt hæmodynamisk respons på anæstesi indledning hos ældre ved sammenligning af thiopental og propofol | |||||||||||||
Medical condition: Induction of anaesthesia in an elderly population | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002374-55 | Sponsor Protocol Number: S3250493 | Start Date*: 2007-08-10 | |||||||||||
Sponsor Name:GlaxoSmithKline Consumer Healthcare | |||||||||||||
Full Title: Simultaneous fMRI/EEG of the 4 mg nicotine lozenge in relief of cognitive impairment associated with nicotine withdrawal | |||||||||||||
Medical condition: Nicotine dependence | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000240-26 | Sponsor Protocol Number: CBD_ADD_IN | Start Date*: 2013-10-29 | |||||||||||
Sponsor Name:King's College London
[...]
1. King's College London
2. South London and Maudsley NHS Foundation Trust |
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Full Title: Cannabidiol as an add-on therapy in treatment-refractory psychotic disorders | |||||||||||||
Medical condition: Schizophrenia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011824-79 | Sponsor Protocol Number: 91686125 | Start Date*: 2009-11-03 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: Effects of fluoxetine on the outgrowth of the serotonergic system | |||||||||||||
Medical condition: We investigate whether the effects fluoxetine (Prozac®) on the outgrowth of the serotonergic system are dependent on age. In a 16 week multicenter randomized, double-blind, placebo controlled trial... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001907-19 | Sponsor Protocol Number: PILOT-PREXOL | Start Date*: 2019-07-03 | |||||||||||
Sponsor Name:Region Skåne | |||||||||||||
Full Title: Pramipexole augmentation to target anhedonia in depression - a pilot study | |||||||||||||
Medical condition: Depression | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
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: 2019-004984-31 | Sponsor Protocol Number: DR180133 | Start Date*: 2021-04-21 |
Sponsor Name:CHRU TOURS | ||
Full Title: Nitrous Oxide in Resistant Depression in Elderly Subjects: A Randomized, Double-blind, Comparator Trial | ||
Medical condition: Resistant Depression in the Elderly Subject | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
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