- Trials with a EudraCT protocol (126)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
126 result(s) found for: Functional medicine.
Displaying page 1 of 7.
EudraCT Number: 2005-003696-20 | Sponsor Protocol Number: ---------------------------- | Start Date*: 2007-05-09 |
Sponsor Name:Donau-universität Krems | ||
Full Title: "TCM- Phythotherapie bei Osteoarthrose von Knie und Hüfte" (TCM-Phythotherapy in the Osteoarthrosis of the knee and hip) | ||
Medical condition: Osteoarthrosis of the knee and hip. - Clinical symptoms due to osteoarthrosis of the knee and hip consisting of pain, stiffness and functional restriction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020698-17 | Sponsor Protocol Number: 2010_3 | Start Date*: 2010-10-04 |
Sponsor Name:Antwerp University Hospital : Department Respiratory Medicine | ||
Full Title: Study of the vascular wall with functional imaging in OSA patients. | ||
Medical condition: Obstructive sleep apnea (OSA) is a prevalent disorder and characterised by sleepiness during the daytime, fatigue and impairments of concentration. OSA can also lead to cardiovascular pathology due... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004415-24 | Sponsor Protocol Number: 09/2011MolecularImaging | Start Date*: 2012-01-16 | |||||||||||
Sponsor Name:IRCCS CENTRO SAN GIOVANNI DI DIO | |||||||||||||
Full Title: Molecular imaging for the early diagnosis and monitoring of Alzheimer’s disease in old individuals with cognitive disturbances: an ADNI-compatible prospective study | |||||||||||||
Medical condition: Mild Congitive Impairment (MCI) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001864-36 | Sponsor Protocol Number: Rikkunshito1 | Start Date*: 2015-10-09 | |||||||||||
Sponsor Name:uzleuven | |||||||||||||
Full Title: A PLACEBO-CONTROLLED STUDY ON THE EFFECT OF RIKKUNSHITO ON GASTRIC ACCOMMODATION AND NUTRIENT TOLERANCE, QUANTIFIED BY INTRAGASTRIC PRESSURE MONITORING DURING INTRAGASTRIC NUTRIENT INFUSION, IN FUN... | |||||||||||||
Medical condition: functional dyspepsia - postprandial distress syndrome | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005389-31 | Sponsor Protocol Number: FBB-HUG-2014 | Start Date*: 2015-02-18 | |||||||||||
Sponsor Name:HôPITAUX UNIVERSITAIRES DE GENèVE | |||||||||||||
Full Title: Incremental diagnostic value of Florbetaben Imaging vs other core biomarkers for Alzheimer Disease in patients with Mild Cognitive Impairment. An Investigator-Initiated Sponsored Study. | |||||||||||||
Medical condition: Mild Cognitive Impairment | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015058-38 | Sponsor Protocol Number: OR09/9018 | Start Date*: 2010-10-22 |
Sponsor Name:University of Leeds | ||
Full Title: Improving the outcome for patients after osteoporotic femoral fractures | ||
Medical condition: OSTEOPOROTIC FEMORAL FRACTURE | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-005466-19 | Sponsor Protocol Number: R0002198 | Start Date*: 2014-05-26 |
Sponsor Name:RadboudUMC | ||
Full Title: Cytokine inhibition in Chronic Fatigue Syndrome patients - a pilot study. | ||
Medical condition: Chronic Fatigue Syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002126-75 | Sponsor Protocol Number: LIN-MD-67 | Start Date*: 2021-10-13 |
Sponsor Name:Allergan | ||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Sequential, Ascending, Multidose Study to Evaluate the Safety and Efficacy of Linaclotide in Pediatric Participants (Age 2 to 5 Years) with ... | ||
Medical condition: Functional Constipation (FC) | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-005285-38 | Sponsor Protocol Number: IM101-591 | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:The University of Leeds | |||||||||||||
Full Title: Phase II proof of concept study of Abatacept (Orencia) in individuals who aRe Considered At risk of Developing Inflammatory Arthritis | |||||||||||||
Medical condition: Inflammatory arthritis | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023366-49 | Sponsor Protocol Number: Bosentan for HPS | Start Date*: 2011-07-22 |
Sponsor Name:Med. Univ. Wien, Univ. Klinikum für Interne Medizin III | ||
Full Title: Bosentan for treatment ofhepatopulmonary syndrome in patients with liver cirrhosis - a prospective double blind randomized controlled clinical study | ||
Medical condition: HPS is by far the most frequent respiratory complication of cirrhosis leading to significantly increased mortality. The only therapeutic option is liver transplantation. Many patients with HPS who ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-017581-22 | Sponsor Protocol Number: 20091003 | Start Date*: 2011-01-04 |
Sponsor Name:Department of Psychiatry and Psychotherapy, Charity University Medicine | ||
Full Title: Cognitive impairment in bipolar disorder treated with aripiprazole | ||
Medical condition: Bipolar disorder is among the most severely debilitating diseases. Patients with bipolar disorder generally experience high rates of relapse, a chronic recurrent course, lingering residual symptoms... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021664-16 | Sponsor Protocol Number: SVUH | Start Date*: 2010-11-04 | |||||||||||
Sponsor Name:Solvotrin Innovations Ltd | |||||||||||||
Full Title: The role of doxycycline in the management of diastolic dysfunction | |||||||||||||
Medical condition: Diastolic dysfunction | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2013-001258-82 | Sponsor Protocol Number: CFTRcysta1 | Start Date*: 2013-09-12 |
Sponsor Name:European Institute for Cystic Fibrosis Research (IERFC) | ||
Full Title: A phase II pilot clinical study of experimental research to evaluate the functional rescue of CFTR protein through proteostasis regulators | ||
Medical condition: Cystic fibrosis patients with F508del-CFTR in homozygous or compound heterozygous with Class I or II mutations | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002998-11 | Sponsor Protocol Number: ENDO-RCA | Start Date*: 2014-11-14 | |||||||||||
Sponsor Name:Rigshospitalet, Capital Region Bloodbank 2034, Section for Transfusion Medicine | |||||||||||||
Full Title: Safety and efficacy of low-dose Iloprost administration and blood pressure target in addition to standard therapy, as compared to standard therapy alone, in post-cardiac- arrest-syndrome patients... | |||||||||||||
Medical condition: Cardiac Arrest | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004160-22 | Sponsor Protocol Number: LUMC_IEMO80PLUS_1.0 | Start Date*: 2013-06-18 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: IEMO 80-plus thyroid trial | ||
Medical condition: Subclinical hypothyroidism | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002263-17 | Sponsor Protocol Number: BRN-C-2017-01 | Start Date*: 2017-11-02 | |||||||||||
Sponsor Name:BOIRON | |||||||||||||
Full Title: Efficacy and safety of Passiflora Compose in patients newly diagnosed with adjustment disorder with anxiety, as first-line treatment, compared to alprazolam | |||||||||||||
Medical condition: Adjustment disorder with anxiety | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004487-25 | Sponsor Protocol Number: KETASELF-1 | Start Date*: 2021-02-08 |
Sponsor Name:Linköpings Universitet | ||
Full Title: Experiencing the self through touch - self-other-distinction in an altered state of self: An exploratory randomized placebo-controlled experimental medicine study | ||
Medical condition: Healthy volunteer. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003853-70 | Sponsor Protocol Number: PNRR-MR1-2022-12375914 | Start Date*: 2023-05-02 | |||||||||||||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||||||||||||
Full Title: Towards a personalized precision medicine in rare disease: tirzepatide (a dual glucose dependent insulinotropic polypeptide and glucagon-like peptide-I receptor agonist) monotherapy in patients wi... | |||||||||||||||||||||||
Medical condition: Wolfram syndrome type 1 | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003858-85 | Sponsor Protocol Number: HFIRONT | Start Date*: 2020-02-24 |
Sponsor Name:Medical University Innsbruck | ||
Full Title: Randomized double-blind explorative controlled clinical trial analyzing the effects of ferric carboxymaltose in patients with iron deficiency and chronic heart failure | ||
Medical condition: This is a randomized double-blind explorative controlled clinical Trial that analyses the effects of 1000mg ferric carboxymaltose in patients with chronic heart failure and iron deficiency. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
