- Trials with a EudraCT protocol (12)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
12 result(s) found for: Water retention.
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EudraCT Number: 2013-000861-36 | Sponsor Protocol Number: ENS/007612 | Start Date*: 2013-05-17 | |||||||||||
Sponsor Name:Ensinger Mineral-Heilquellen GmbH | |||||||||||||
Full Title: Double-blind, randomized, placebo-controlled clinical trial to evaluate the safety and efficacy of „Ensinger Schiller Quelle Heilwasser“ on improvement of bowel function | |||||||||||||
Medical condition: - Functional constipation according to the ROME III criteria - The subjects have bowel movements 2 - 4 days/week | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001846-24 | Sponsor Protocol Number: 1 | Start Date*: 2016-06-29 |
Sponsor Name:Antwerp University Hospital | ||
Full Title: Metabolism of Isotonic versus Hypotonic Maintenance Solutions in fasting healthy Adults (MIHMoSA), a Single-Blind Randomized Crossover Trial | ||
Medical condition: Healthy adult volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-001634-28 | Sponsor Protocol Number: CVMD-DU-087 | Start Date*: 2008-11-11 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Identification of genetic and functional biomarkers that predict PPAR-gamma-associated fluid retention and oedema | |||||||||||||
Medical condition: Patients with Type 2 diabetes mellitus (T2DM) whoa re not receiving insulin treatment | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000664-14 | Sponsor Protocol Number: 16178SE-AS | Start Date*: 2018-02-06 |
Sponsor Name:Belfast Health and Social Care Trust | ||
Full Title: A 2x2 factorial randomised examiner blind open label trial to determine the CLinical and cost- Effectiveness of hypertonic saline (HTS 6%) and carbocisteine for Airway cleaRance versus usual care o... | ||
Medical condition: Bronchiectasis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002742-42 | Sponsor Protocol Number: 2013DM19 | Start Date*: 2014-12-23 |
Sponsor Name:University of Dundee/ NHS Tayside | ||
Full Title: Research into the Effect Of SGLT2 inhibition on left ventricular Remodelling in patients with heart failure and diabetes Mellitus | ||
Medical condition: Type 2 diabetes and Heart Failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005342-63 | Sponsor Protocol Number: UoL001206 | Start Date*: 2016-06-23 |
Sponsor Name:University of Liverpool | ||
Full Title: Mindex: The efficacy and safety of very low dose dexamethasone used to facilitate the extubation of ventilator dependent preterm babies who are at high risk of bronchopulmonary dysplasia | ||
Medical condition: Bronchopulmonary dysplasia | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002275-33 | Sponsor Protocol Number: 0805-2012-1 | Start Date*: 2014-01-15 |
Sponsor Name:Dept. of Gastroenterology, Universityhospital Odense | ||
Full Title: Renal and cardiac effects of terlipressin and dobutamin in cirrhosis and ascites. A randomised study. | ||
Medical condition: Liver cirrhosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002359-14 | Sponsor Protocol Number: Lact-004-CP4 | Start Date*: 2018-10-17 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Blood Glucose Response After Oral Intake of Lactulose (Laevolac®) in Mildly Constipated Patients with Diabetes Mellitus Type 2 | |||||||||||||
Medical condition: Symptomatic treatment of constipation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001351-31 | Sponsor Protocol Number: ED17/93260 | Start Date*: 2017-09-04 | |||||||||||
Sponsor Name:University of Leeds | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled phase II pilot trial investigating efficacy, safety and feasibility of 11β-hydroxysteroid dehydrogenase type 1 inhibition by AZD4017 to improve skin f... | |||||||||||||
Medical condition: Type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002088-29 | Sponsor Protocol Number: DFR2593-307 | Start Date*: 2007-08-22 | |||||||||||
Sponsor Name:Rheoscience A/S | |||||||||||||
Full Title: Efficacy and Safety of Treatment with Balaglitazone in Type 2 Diabetes Patients on Stable Insulin Therapy | |||||||||||||
Medical condition: Balaglitazone is being developed as an oral anti-diabetic drug to improve glycaemic control in patients with type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022364-12 | Sponsor Protocol Number: BAY86-5321/91745 | Start Date*: 2011-03-18 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A randomized, double masked, active controlled, phase III study of the efficacy and safety of repeated doses of intravitreal VEGF Trap-Eye in subjects with diabetic macular edema | |||||||||||||
Medical condition: Diabetic macular edema with central involvement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) CZ (Completed) ES (Completed) DK (Completed) IT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004825-14 | Sponsor Protocol Number: D1680C00016 | Start Date*: 2016-05-04 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: A 24-Week, Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Study to Investigate the Effects of Saxagliptin, Saxagliptin Combined with Dapagliflozin, and Sitagliptin in Pat... | |||||||||||||
Medical condition: Patients with type 2 diabetes mellitus and heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) HU (Completed) BG (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
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