- Trials with a EudraCT protocol (3,168)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
3,168 result(s) found for: Intervention.
Displaying page 66 of 159.
EudraCT Number: 2021-006512-87 | Sponsor Protocol Number: PHERFLOT | Start Date*: 2022-09-26 | ||||||||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH | ||||||||||||||||||
Full Title: Pembrolizumab and trastuzumab in combination with FLOT in the perioperative treatment of HER2-positive, localized esophagogastric adenocarcinoma - A phase II trial of the AIO study group – PHERFLOT – | ||||||||||||||||||
Medical condition: HER2 positive, localized esophagogastric adenocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002844-25 | Sponsor Protocol Number: SM1-JOAST-2019 | Start Date*: 2019-11-26 | ||||||||||||||||
Sponsor Name:Daniel Hägi-Pedersen | ||||||||||||||||||
Full Title: Effect of Combinations of Paracetamol, Ibuprofen, and Dexamethasone on Patient-Controlled Morphine Consumption in the First 24 Hours After Total Hip Arthroplasty. The RECIPE Randomized Clinical Trial | ||||||||||||||||||
Medical condition: Acute postoperative pain after hip arthroplasty | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002571-11 | Sponsor Protocol Number: ENHANCE | Start Date*: 2022-11-25 | |||||||||||
Sponsor Name:Institut Mutualiste Montsouris | |||||||||||||
Full Title: EvaluatioN of High-Intensity Focused Ultrasound (HIFU) Hemi-ablation and short-term AndrogeN deprivation therapy Combination to Enhance prostate control for intermediate risk localized prostate can... | |||||||||||||
Medical condition: Intermediate risk localized prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005533-20 | Sponsor Protocol Number: VOLATILE10600 | Start Date*: 2014-12-11 |
Sponsor Name:OSPEDALE SAN RAFFAELE IRCCS | ||
Full Title: VOLATILE ANESTHETICS TO REDUCE MORTALITY IN CARDIAC SURGERY. A MULTICENTRE RANDOMIZED CONTROLLER STUDY | ||
Medical condition: PATIENTS UNDERGOING CORONARY ARTERY BYOASS GRAFT SURGERY | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003570-26 | Sponsor Protocol Number: CLN-PRO-V011 | Start Date*: 2019-09-07 | ||||||||||||||||
Sponsor Name:Humacyte, Inc. | ||||||||||||||||||
Full Title: A Phase 2 Assessment of Humacyte’s Human Acellular Vessel in Patients Needing Vascular Access for Dialysis | ||||||||||||||||||
Medical condition: End-stage renal disease (ESRD) requiring placement of an arteriovenous (AV) graft in the arm (upper- or forearm) for dialysis access. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002000-39 | Sponsor Protocol Number: 212602 | Start Date*: 2020-09-29 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: B-Fine: An open label, single arm study to mechanistically interrogate the therapeutic effect of GSK3228836 in patients with Chronic Hepatitis B via intrahepatic immunophenotyping | |||||||||||||
Medical condition: Chronic Hepatitis B | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004358-14 | Sponsor Protocol Number: BVDStudy | Start Date*: 2017-01-18 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA ARCISPEDALE SANTA MARIA NUOVA/IRCCS DI REGGIO EMILIA | |||||||||||||
Full Title: Bromfenac 0.09% versus dexamethasone 0.1% ophthalmic solutions to reduce inflammation after cataract surgery: the BVD Study. | |||||||||||||
Medical condition: Postoperative ocular inflammation after cataract surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001365-32 | Sponsor Protocol Number: 19CX5006 | Start Date*: 2019-07-25 | |||||||||||
Sponsor Name:Imperial Joint Research Compliance Office | |||||||||||||
Full Title: IP4- CHRONOS: Comparative Health Research Outcomes of NOvel Surgery in Prostate Cancer | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005130-15 | Sponsor Protocol Number: 2019/ABM/01/00009 | Start Date*: 2021-09-30 | |||||||||||
Sponsor Name:Nicolaus Copernicus University in Torun | |||||||||||||
Full Title: Evaluation of safety and efficacy of two ticagrelor-based de-escalation antiplatelet strategies in acute coronary syndrome: the randomized, multicentre, double-blind ELECTRA RCT study. | |||||||||||||
Medical condition: Acute Coronary Syndrom (ACS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-004155-13 | Sponsor Protocol Number: BMS_IM101-931 | Start Date*: 2023-04-20 | |||||||||||
Sponsor Name:Universitätsklinikum Freiburg | |||||||||||||
Full Title: Study to investigate the restoring of an immunological balance during therapy with abatacept Abatacept restores immune system equilibrium (ARISE) | |||||||||||||
Medical condition: CVID patients confirmed according to ESID/PAGID criteria or related disorders which fulfill the diagnostic criteria for CVID and interstitial lung disease or granuloma diagnosed by chest CT positiv... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004482-88 | Sponsor Protocol Number: FAR-DOL-2015 | Start Date*: 2016-04-25 | |||||||||||
Sponsor Name:Fundació Parc Taulí | |||||||||||||
Full Title: Randomized clinical trial to compare the safety and effectiveness of metamizol, ibuprofen and tramadol added to a fixed dose of paracetamol in the treatment of post- surgical pain in patients ? 80 ... | |||||||||||||
Medical condition: The medical condition being studied is post surgical pain following surgery for femur fracture in patients ? 80 years old | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000573-80 | Sponsor Protocol Number: APHP201075 | Start Date*: 2021-05-10 |
Sponsor Name:APHP DRCI | ||
Full Title: Acute Myocardial infarction Upbound to percutaneous coronary intervention, immediately (STEMI) or in the Next three Days (NSTEMI), and randomized to Subcutaneous Evolocumab or Normal strategies to ... | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-002839-66 | Sponsor Protocol Number: IMVT-1401-3203 | Start Date*: 2023-09-07 | |||||||||||
Sponsor Name:Immunovant Sciences, GmbH | |||||||||||||
Full Title: An Open-label Extension Study for Participants who Completed Study IMVT-1401-3201 or Study IMVT-1401-3202 to Assess the Efficacy and Safety of Batoclimab for the Treatment of Thyroid Eye Disease (TED) | |||||||||||||
Medical condition: Thyroid Eye Disease (TED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Not Authorised) LV (Trial now transitioned) BE (Trial now transitioned) HU (Trial now transitioned) SK (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002015-22 | Sponsor Protocol Number: Strindfors2 | Start Date*: 2022-08-12 | |||||||||||
Sponsor Name:Dept. of Obstetrics and Gynecology, Sodersjukhuset | |||||||||||||
Full Title: A pilot study and randomized placebo-controlled trial on the effect and timing of oral Tranexamic acid (TA) administered prepartum on postpartum haemorrhage after vaginal delivery | |||||||||||||
Medical condition: Postpartum hemorrhage which is defined as bleeding during and after delivery that exceeds 500 ml. It is most commonly due to an atony of the uterus but may also have other causes such as tissue dam... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002453-25 | Sponsor Protocol Number: MERCURI-2 | Start Date*: 2023-03-07 | |||||||||||
Sponsor Name:Amsterdam UMC | |||||||||||||
Full Title: Preoperative sodium glucose cotransporter 2 inhibitors for prevention of postoperative acute kidney injury in cardiac surgery patients – a randomized, placebo-controlled, multi-centre, phase IV cli... | |||||||||||||
Medical condition: Cardiac Surgery-Associated Acute Kidney Injury | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005001-26 | Sponsor Protocol Number: 20-773/M | Start Date*: 2021-12-24 |
Sponsor Name:UMC Utrecht | ||
Full Title: Influencing Progression of Airway Disease in Primary Antibody Deficiency | ||
Medical condition: Primary antibody deficiency: - Unclassified antibody deficiency (unPAD) - IgA deficiency - Specific polysaccharide antibody deficiency (SPAD) - IgG subclass deficiency (IgSD) - Common variable immu... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002466-13 | Sponsor Protocol Number: NICITA | Start Date*: 2019-10-23 | |||||||||||
Sponsor Name: Institut für Klinische Krebsforschung IKF GmbH | |||||||||||||
Full Title: Nivolumab with chemotherapy in pleural mesothelioma after surgery | |||||||||||||
Medical condition: Malignant Pleural Mesothelioma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001560-19 | Sponsor Protocol Number: CSCC-ASC2 | Start Date*: 2015-06-29 | |||||||||||
Sponsor Name:Department of Cardiology, Rigshospitalet | |||||||||||||
Full Title: Allogeneic adipose tissue-derived stromal/stem cell therapy in patients with ischemic heart disease and heart failure | |||||||||||||
Medical condition: Ischemic heart disease and heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000608-40 | Sponsor Protocol Number: No-DAPT-TAVI | Start Date*: 2018-07-06 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: Aspirin versus Aspirin plus Clopidogrel in Patients Undergoing Transcatheter Aortic Valve Replacement: a Randomized Multicenter Study | |||||||||||||
Medical condition: valvular aortic stenosis submitted to TAVI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003700-31 | Sponsor Protocol Number: ImNuT | Start Date*: 2017-10-11 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Effects of nutrition therapy on growth, metabolism and inflammation in immature infants; a double-blind randomized, controlled trial | ||
Medical condition: To determine whether early and prolonged supply of ARA and DHA improves quality of growth and clinical outcomes in extreme premature infants as compared to our present nutrient supply. By closely a... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
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