- Trials with a EudraCT protocol (127)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
127 result(s) found for: Cooperation.
Displaying page 1 of 7.
EudraCT Number: 2013-003991-11 | Sponsor Protocol Number: S55859 | Start Date*: 2013-12-03 |
Sponsor Name:Katholieke Universiteit Leuven | ||
Full Title: Optimization of procedural sedation protocol used for dental care delivery in people with mental disability | ||
Medical condition: Limited cooperation of people with mental disability during regular dental care delivery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-004555-79 | Sponsor Protocol Number: 16-115 | Start Date*: 2017-08-08 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: Impact of preoperative midazolam on outcome of elderly patients: a multicenter randomised controlled trial | ||
Medical condition: Under investigation are elderly patients (≥65 years of age) undergoing each kind of surgery with planned general or combined regional and general anaesthesia. Primary, we will investigate the posto... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002249-11 | Sponsor Protocol Number: BLQ-01-003-04 | Start Date*: 2004-09-20 |
Sponsor Name:BAUSCH&LOMB - IOM S.P.A. | ||
Full Title: Double blind, randomized, multicenter, placebo-controlled, parallel-group design clinical trial of the efficacy and tolerability of cloriclomene hydrochloride capsules 100 mg TID in diabetic patien... | ||
Medical condition: Mild to moderate non-proliferative diabetic retinopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2004-002065-20 | Sponsor Protocol Number: RD-5103-025-04 | Start Date*: 2005-03-09 |
Sponsor Name:Derbyshire NHS Trust | ||
Full Title: Single site randomised trial of fibrin tissue glue versus surgery in the treatment of pilonidal sinus | ||
Medical condition: Pilonidal sinus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-000755-13 | Sponsor Protocol Number: DACLEAN | Start Date*: 2020-03-31 | |||||||||||
Sponsor Name:CHU de Poitiers | |||||||||||||
Full Title: ESTIMATION OF THE INCIDENCE OF COLONIZATION OF PERIPHERAL VENOUS CATHETERS AFTER SKIN DISINFECTION WITH 0.5% SODIUM HYPOCHLORITE, PRECEDED OR NOT BY AN APPLICATION OF 70% ETHANOL: PILOT, MONOCENTRI... | |||||||||||||
Medical condition: Bacterial colonization of peripheral venous catheters | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001468-21 | Sponsor Protocol Number: KIIOIW001 | Start Date*: 2006-08-24 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Sympthomatic and prophylactic treatment of drug induced oral dryness in elderly patients with high drug consumption. | ||
Medical condition: Oral dryness is a common problem with serious consquences, especially among elderly individuals. The most common reason for oral dryness is drug consumption. Research has shown that an individual w... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000192-27 | Sponsor Protocol Number: GutHeart1 | Start Date*: 2015-03-19 |
Sponsor Name:Oslo University Hospital | ||
Full Title: GutHeart: Targeting Gut microbiota to treat Heart failure | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021518-45 | Sponsor Protocol Number: ARA290_PAIN_v1 | Start Date*: 2010-07-12 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: A pilot study on the effect of ARA290 on pain and pain responses and retinal edema in patients with diabetes mellitus and neuropathic pain | |||||||||||||
Medical condition: Neuropathic pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000907-27 | Sponsor Protocol Number: D2782C00010 | Start Date*: 2008-10-24 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II, Single Arm, Single Agent, Multicentre, Adaptive 2-Stage Study to Evaluate the Efficacy, Safety and Pharmacokinetics of AZD4877 Administered Weekly in Patients with Recurrent Advanced Ur... | ||
Medical condition: Stage IV urothelial Cancer Cáncer de urotelio estadío 4 | ||
Disease: | ||
Population Age: | Gender: Male, Female | |
Trial protocol: ES (Completed) DE (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002567-27 | Sponsor Protocol Number: CTU 011 B | Start Date*: 2008-11-04 |
Sponsor Name:RIEMSER Arzneimittel AG | ||
Full Title: CLINICAL PHASE III MULTI-CENTRIC, DOUBLE-BLIND, DOUBLE DUMMY, RANDOMISED STUDY TO COMPARE SAFETY AND EFFICACY OF DOPRAM® (DOXAPRAM HYDROCHLORIDE) TO CAFEINE COOPER (CAFFEINE CITRATE) IN THE TREATME... | ||
Medical condition: Premature infants with a corrected gestational age of 25;0 to 30;6 weeks with a immature central nervous system resulting in frequent apnoeic episodes | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002838-36 | Sponsor Protocol Number: CIBOMA/2004-01 | Start Date*: 2005-11-30 |
Sponsor Name:COALICIÓN IBEROAMERICANA DE INVESTIGACIÓN EN ONCOLOGÍA MAMARIA (CIBOMA) | ||
Full Title: PHASE IV.III, MULTICENTER, OPEN, RANDOMIZED TREATMENT STUDY TO EVALUATE THE EFFICACY OF MAINTENANCE THERAPY WITH CAPECITABINE (X) AFTER STANDARD ADJUVANT CHEMOTHERAPY IN PATIENTS WITH OPERABLE, HOR... | ||
Medical condition: Patients with operated breast cancer with no metastatic involvement (AJCC, 2002). Patients will be able to participate whether they present axillary node involvement (node positive) or not (node n... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005835-87 | Sponsor Protocol Number: GBG41 | Start Date*: 2006-08-16 |
Sponsor Name:GermanBreastGroup | ||
Full Title: A randomized discontinuation phase II study to determine the efficacy of RAD001 in breast cancer patients with bone metastases | ||
Medical condition: Bone metasatsis, Breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000074-51 | Sponsor Protocol Number: GBG 39 | Start Date*: 2005-05-03 |
Sponsor Name:GBG Forschungs GmbH | ||
Full Title: A multicenter phase II study to determine the efficacy of capecitabine as first line monochemotherapy in patients with HER2 negative, medium-risk, metastatic breast cancer | ||
Medical condition: patients with HER2 negative metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023044-32 | Sponsor Protocol Number: DCS-fMRIPanik | Start Date*: 2011-08-10 |
Sponsor Name:Charité Universitaetsmedizin Berlin | ||
Full Title: Mechanisms of action in exposure therapy: Decoding the neural basis of fear extinction and its pharmacological modulation in patients with panic disorder | ||
Medical condition: panic disorder and agoraphobia | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001398-19 | Sponsor Protocol Number: Exposition-DCS | Start Date*: 2011-06-27 |
Sponsor Name:Charité Universitätsmedizin Berlin | ||
Full Title: D-cycloserine augmented exposure therapy in patients with agoraphobia | ||
Medical condition: agarophobia with or without panic disorder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001736-57 | Sponsor Protocol Number: 20190416MH | Start Date*: 2019-06-24 | ||||||||||||||||
Sponsor Name:St Olavs Hospital | ||||||||||||||||||
Full Title: ULTRASOUND-ENHANCED UPTAKE OF CHEMOTHERAPY IN PATIENTS WITH INOPERABLE PANCREATIC DUCTAL ADENOCARCINOMA | ||||||||||||||||||
Medical condition: Pancreatic cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NO (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002701-11 | Sponsor Protocol Number: ACE | Start Date*: 2016-06-13 |
Sponsor Name:Oslo University Hospital | ||
Full Title: ADJUVANT CHEMOTHERAPY IN ELDERLY – GERIATRIC ASSESSMENT AND PROGNOSTIC GENE SIGNATURES | ||
Medical condition: undergone R0-resection of for colon cancer stage III | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2022-003202-77 | Sponsor Protocol Number: NEOKOFF22 | Start Date*: 2023-04-04 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name: | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: The effect of additional pre-extubational loading dose of caffeine-citrate | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Extubation failure and bronchopulmonary dysplasia | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: HU (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006253-41 | Sponsor Protocol Number: DC-004 | Start Date*: 2012-01-05 |
Sponsor Name:The Norwegian Radium Hospital, Oslo University Hospital | ||
Full Title: Phase I/II trial for vaccine therapy with hTERT-, survivin- and tumor cell derived mRNA + ex vivo T cell expansion and reinfusion in patients with metastatic malignant melanoma | ||
Medical condition: Malignant melanoma stage IV M1c or better | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000815-26 | Sponsor Protocol Number: LUCID | Start Date*: 2013-08-26 |
Sponsor Name:Oslo University Hospital | ||
Full Title: THE OSLO STUDY OF CLONIDINE IN ELDERLY PATIENTS WITH DELIRIUM | ||
Medical condition: Delirium in elderly patients admitted to the acute geriatric ward | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
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