- Trials with a EudraCT protocol (542)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (41)
542 result(s) found for: Internal.
Displaying page 1 of 28.
| EudraCT Number: 2007-004526-24 | Sponsor Protocol Number: Panbio/CR/0042006/CT | Start Date*: 2008-09-23 | |||||||||||
| Sponsor Name:Panacea Biotec Ltd | |||||||||||||
| Full Title: A double-blind, randomized, placebo-controlled, multicentre study to assess the efficacy and safety of Euphorbia Prostrata Dry Extract Tablets in patients of 1° and 2° internal haemorrhoids | |||||||||||||
| Medical condition: Male and female subjects, at least 18 years of age with a diagnosis of internal haemorrhoids (1° and 2°) confirmed by protoscopic examination and suffering form an uncomplicated and untreated acute... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-005175-18 | Sponsor Protocol Number: 151610/06 | Start Date*: 2007-09-27 |
| Sponsor Name:Dpt. of Internal Medicine, Medical University of Innsbruck | ||
| Full Title: Influence of insulin Levemir on endothelial function in type 2 diabetes mellitus. A prospective case-control study. | ||
| Medical condition: Patients with known history of type 2 Diabetes Mellitus longer than 6 months, who were treated by diet in combination with oral antidiabetic drugs (OADs) are to be included in the study. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: AT (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003281-84 | Sponsor Protocol Number: EXCRETE | Start Date*: 2018-03-27 |
| Sponsor Name:Academical Medical Centre, department of internal | ||
| Full Title: The Effect of UrsodeoXyCholicacid (UDCA) and ezetimibe on total faecal steRol ExcreTion and plasma lipid lEvels | ||
| Medical condition: Familial hypercholesterolemia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005522-22 | Sponsor Protocol Number: Rifa-BP | Start Date*: 2012-01-23 |
| Sponsor Name:Oulu University Hospital, Department of Internal Medicine | ||
| Full Title: The effects of PXR activation on blood pressure regulation | ||
| Medical condition: Healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002335-27 | Sponsor Protocol Number: IGG-VIJA-001 | Start Date*: 2005-09-01 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Botulin Toxin injection for the treatment of Internal Anal Sphincter Achalasia | |||||||||||||
| Medical condition: Treatment of internal anal sphincter achalasia | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004106-87 | Sponsor Protocol Number: CAS CVVH | Start Date*: 2007-10-23 |
| Sponsor Name:Meical University, Dpt. Internal Medicine, Div. of General Internal Medicine | ||
| Full Title: CLINICAL PHARMACOKINETICS OF CASPOFUNGIN IN CRITICALLY ILL PATIENTS DURING CONTINUOUS VENO-VENOUS HEMOFILTRATION | ||
| Medical condition: Plasma concentrations of Caspofungin will be measured in patients requiring treatment with Cancidas (Caspofungin) and continuous veno-venous hemofiltration | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-004107-20 | Sponsor Protocol Number: CAS ELF | Start Date*: 2007-10-23 |
| Sponsor Name:Medical University, Dpt. Internal Medicine, Div. of General Internal Medicine | ||
| Full Title: LUNG PENETRATION OF CASPOFUNGIN INTO EPITHELIAL LINING FLUID | ||
| Medical condition: Plasma and ELF concentrations of Caspofungin will be measured in patients requiring treatment with Cancidas (Caspofungin) for fungal infection (proven or suspected) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004170-25 | Sponsor Protocol Number: MH-110 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Bracco Imaging S.p.A. | ||
| Full Title: A PHASE III, MULTI-CENTER, OPEN-LABEL STUDY TO EVALUATE SAFETY AND EFFICACY OF MULTIHANCE® AT THE DOSE OF 0.10 mmol/kg IN MAGNETIC RESONANCE IMAGING OF THE CENTRAL NERVOUS SYSTEM IN PEDIATRIC PA... | ||
| Medical condition: imaging diagnosis of highly suspected or known brain and/or spine disease, which are known to impair the Blood Brain Barrier Function | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Completed) BE (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-003347-10 | Sponsor Protocol Number: PXR-HDL | Start Date*: 2017-01-16 |
| Sponsor Name:Oulu University Hospital, Internal Medicine Research Unit | ||
| Full Title: The effects of PXR activation on HDL-cholesterol | ||
| Medical condition: Healthy volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2023-000007-39 | Sponsor Protocol Number: N/A. | Start Date*: 2023-03-23 | |||||||||||
| Sponsor Name:Aarhus University Hospital, Department of Endocrinology and Internal Medicine | |||||||||||||
| Full Title: Bisphosphonate vs. Placebo Prior to Parathyroidectomy in Primary Hyperparathyroidisme: A Randomized, blinded Placebo-controlled Trial | |||||||||||||
| Medical condition: Osteopenia i.e. bone mineral density T-score < -1 in patients with primary hyperparathyroidism | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-003842-27 | Sponsor Protocol Number: Studio-flourochinoloni-in-BPCO. | Start Date*: 2008-10-14 |
| Sponsor Name:CENTRO STUDI FADOI | ||
| Full Title: Randomized, single-blind, parallel groups, controlled study to compare levofloxacin and prulifloxacin in patients with exacerbations of COPD previously treated with different antibiotics and admitt... | ||
| Medical condition: - Patients with acute exacerbation of COPD of possible infectious origin, previously treated with antibiotic therapy (no quinolones), without clinical improvement, and hospitalized in Internal Medi... | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-004078-53 | Sponsor Protocol Number: 83403 | Start Date*: 2023-08-22 |
| Sponsor Name:Academic Medical Center (AMC), department of Internal Medicine | ||
| Full Title: Specifying the anti-inflammatory effects of ziltivekimab with diverse imaging modalities and in-depth cellular phenotyping | ||
| Medical condition: - Plaque characteristics - Systemic inflammation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-003168-28 | Sponsor Protocol Number: 77458 | Start Date*: 2022-06-28 |
| Sponsor Name:Academic Medical Center (AMC), department of Internal Medicine | ||
| Full Title: Impact of Triglyceride-Lowering on Inflammatory Activity in Patients with Hypertriglyceridemia | ||
| Medical condition: - Hypertriglyceridemia - Inflammation - Lipoproteins | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-005717-19 | Sponsor Protocol Number: Lakritsi001 | Start Date*: 2007-12-04 |
| Sponsor Name:Oulu University Hospital Department of Internal Medicine | ||
| Full Title: Lakritsin ja tiatsididiureetin yhteiskäytön vaikutus kaliumpitoisuuteen | ||
| Medical condition: Terveitä vapaaehtoisia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FI (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000911-26 | Sponsor Protocol Number: Uni-Koeln-1392 | Start Date*: 2011-05-12 |
| Sponsor Name:University of Cologne | ||
| Full Title: Heart rate control after acute myocardial infarct | ||
| Medical condition: successful percutaneous intervention in patients with acute ST-elevated myocardial infarct | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-000266-21 | Sponsor Protocol Number: ABCD HEP | Start Date*: 2007-07-19 |
| Sponsor Name:Medical University, Dpt. Internal Medicine, Div. of General Internal Medicine | ||
| Full Title: PHARMAKOKINETIK VON KOLLOIDALEM AMPHOTERICIN B BEI KRITISCH KRANKEN MIT EINGESCHRÄNKTER LEBERFUNKTION (Pharmacokinetics of colloidal Amphotericin B in critically ill Patients with hepatic impairme... | ||
| Medical condition: Plasma concentrations of colloidal Amphotericin B will be measured in critically ill Patients with hepatic impairment and with normal liver function, both requiring treatment with Amphocil, to dete... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003609-96 | Sponsor Protocol Number: AMB ELF | Start Date*: 2005-09-07 |
| Sponsor Name:Medical University, Dpt. Internal Medicin, Division of General Internal Medicine | ||
| Full Title: Amphotericin B Spiegel in bronchoalveolären Lavagen (Epithelial Lining Fluid) unter Behandlung mit lipidformuliertem Amphotericin B (Amphotericin B levels in broncho-alveolar lavage [epithelial lin... | ||
| Medical condition: Plasma and ELF concentrations of lipidformulatied amphotericin b will be measured in patients requiring treatment with lipid-formulated amphotericin B for fungal pneumonia (proven or suspected). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-012034-70 | Sponsor Protocol Number: AGO/2009/004 | Start Date*: 2009-06-03 |
| Sponsor Name:University Hospital Ghent | ||
| Full Title: A protocol based treatment for debilitating fibrosing skin disorders with (anti-CD-20), rituximab | ||
| Medical condition: Fibrosing skin disorders | ||
| Disease: | ||
| Population Age: | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-003946-18 | Sponsor Protocol Number: GDX-44-011 | Start Date*: 2019-05-03 | |||||||||||
| Sponsor Name:GUERBET | |||||||||||||
| Full Title: Efficacy and safety of gadopiclenol for body magnetic resonance imaging (MRI) | |||||||||||||
| Medical condition: Patients presenting with know or suspected enhancing abnormality(ies) and/or lesion(s) in at least one body region among head & neck, thorax (including breast), abdomen (including liver, pancreas a... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) HU (Completed) BG (Completed) DE (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-005022-38 | Sponsor Protocol Number: T366/2017 | Start Date*: 2018-06-13 | ||||||||||||||||
| Sponsor Name:Turku University Hospital | ||||||||||||||||||
| Full Title: Oxytocin in mr guided focused ultrasound treatment (MRI-HIFU) | ||||||||||||||||||
| Medical condition: women with uterine fibroids or adenomyosis | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: FI (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
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