- Trials with a EudraCT protocol (317)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
317 result(s) found for: Vascular tissue.
Displaying page 1 of 16.
EudraCT Number: 2015-003674-32 | Sponsor Protocol Number: 1.1:12-6-2015 | Start Date*: 2016-02-23 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The effect of Telmisartan on inflammatory processes in the vascular wall of abdominal aortic aneurysms. | ||
Medical condition: Abdominal aortic aneurysm with an indication for elective open surgical repair. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005720-15 | Sponsor Protocol Number: CLZC696A2224 | Start Date*: 2013-09-11 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A randomized, double-blind, active-controlled, parallel group, 52-week study to evaluate the effect of LCZ696 compared to olmesartan on regional aortic stiffness in subjects with essential hyperten... | ||||||||||||||||||
Medical condition: Hypertensive patients. | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001096-43 | Sponsor Protocol Number: PHRN14-AM/PERFORMUS | Start Date*: 2015-07-10 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Treatment of superficial voluminous complicated slow-flow vascular malformations with sirolimus: a phase 2 trial in children observational-phase designed | |||||||||||||
Medical condition: vascular malformations | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002935-27 | Sponsor Protocol Number: 41208 | Start Date*: 2012-12-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Maastricht University Medical Center | |||||||||||||||||||||||||||||||||
Full Title: Diagnostic value of novel MR imaging techniques for the primary staging and restaging of rectal cancer | |||||||||||||||||||||||||||||||||
Medical condition: rectal cancer | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001478-14 | Sponsor Protocol Number: 071301 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Baxalta Innovations GmbH | ||||||||||||||||||
Full Title: A PROSPECTIVE, PHASE 3, OPEN LABEL, INTERNATIONAL MULTICENTER STUDY ON EFFICACY AND SAFETY OF PROPHYLAXIS WITH rVWF IN SEVERE VON WILLEBRAND DISEASE | ||||||||||||||||||
Medical condition: Hereditary severe von Willebrand Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IT (Completed) CZ (Completed) NL (Completed) ES (Completed) DE (Completed) FI (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012086-66 | Sponsor Protocol Number: T05018-1001 | Start Date*: 2009-12-01 | |||||||||||
Sponsor Name:Grifols Inc | |||||||||||||
Full Title: A Phase 1/2a, Open Label, Dose Escalation, Safety Study of Intra-thrombus Plasmin (Human) Administration in Acute, Middle Cerebral Artery, Ischemic Stroke | |||||||||||||
Medical condition: Thrombus in acute ischemic stroke of the middle cerebral artery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) FR (Completed) SK (Completed) AT (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2006-001935-23 | Sponsor Protocol Number: NZHD02 | Start Date*: 2006-10-17 |
Sponsor Name:University of Heidelberg | ||
Full Title: Real-time contrast-enhanced sonography of renal transplant recipients accurately predicts vascular allograft nephropathy | ||
Medical condition: Vascular allograft nephropathy represents the main cause of renal allograft loss after 1 yr of transplantation. The trial shall find a way for early diagnostics. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-009956-20 | Sponsor Protocol Number: ICG-REG_01 | Start Date*: 2009-05-29 | |||||||||||
Sponsor Name:Free State of Bavaria rep. by the Univ. of Regensburg, rep. by the Regensburg Univ. Hospital | |||||||||||||
Full Title: Prospective, randomized, controlled, mono-centric, two-armed, single-blinded pilot study for the treatment of venous and capillary vascular malformations by Indocyanine Green-augmented laser therapy | |||||||||||||
Medical condition: venous and capillary vascular malformations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005612-41 | Sponsor Protocol Number: 15-15 | Start Date*: 2015-11-30 | |||||||||||||||||||||||||||||||
Sponsor Name:Meander Medical Centre | |||||||||||||||||||||||||||||||||
Full Title: Vitamin c to Improve Tissue healing by Administration of Multiple INtravenous dosages | |||||||||||||||||||||||||||||||||
Medical condition: Patients with planned revascularisation surgery on the lower extremities. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001397-15 | Sponsor Protocol Number: BMMNC_CLI_001 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:Institut klinické a experimentální medicíny | |||||||||||||
Full Title: A prospective, randomized study to compare the effect on tissue oxygenation and clinical outcome of autologous bone marrow-derived mononuclear cell therapy with standard treatment in patients with ... | |||||||||||||
Medical condition: Autologous cell therapy (ACT) is new technique for patients with critical limb ischemia and diabetic foot (DF). In our study, the effect of ACT and also the repetitive treatment will be compared wi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001633-40 | Sponsor Protocol Number: ESRA | Start Date*: 2022-03-07 | |||||||||||
Sponsor Name:Thoraxklinik Heidelberg gGmbH | |||||||||||||
Full Title: Efficacy and safety of riociguat (MK-4836) in incipient pulmonary vascular disease as an indicator for early pulmonary arterial Hypertension Doubleblind, randomized, multicentre, multinational, pla... | |||||||||||||
Medical condition: early pulmonary vascular disease, defined as either a) mean pulmonary arterial pressure (mPAP) ≥25 mmHg with pulmonary vascular resistance (PVR) ≥2 to <3 WU and pulmonary arterial wedge pressure (P... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002834-36 | Sponsor Protocol Number: Retro-001 | Start Date*: 2012-09-13 |
Sponsor Name:UMCG | ||
Full Title: Evaluation of the effects of the addition of atropine during propofol/remifentanil induction of anesthesia on hemodynamics, microvascular blood flow and tissue oxygenenation in patients undergoing ... | ||
Medical condition: ophthalmic surgery | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001108-11 | Sponsor Protocol Number: EORTC protocol 62033 | Start Date*: 2004-11-08 | |||||||||||
Sponsor Name:European Organisation for the Research and Treatment of Cancer | |||||||||||||
Full Title: A phase II study of intravenous TZT-1027, administered weekly times two, every three weeks, to patients with advanced or metastatic soft tissue sarcomas (STS) with prior exposure to doxorubicin-bas... | |||||||||||||
Medical condition: Soft Tissue Sarcoma (STS) is a rare group of heterogeneous mesenchymal cancers originating from connective tissue. There are multiple histological subtypes of STS. At present all these subtypes are... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003859-12 | Sponsor Protocol Number: 12-027 | Start Date*: 2013-07-19 | ||||||||||||||||
Sponsor Name:RWTH Aachen University for the Medical Faculty, represented by Clinical Trial Center Aachen (CTC-A) | ||||||||||||||||||
Full Title: Linagliptin as a modulator of vascular inflammation in patients with type 2 diabetes mellitus | ||||||||||||||||||
Medical condition: patients with type 2 diabetes mellitus and vascular inflammation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002247-20 | Sponsor Protocol Number: UIAPB-PRP-2012 | Start Date*: 2012-11-28 | |||||||||||
Sponsor Name:Comarca Ezkerraldea-Enkarterri (OSAKIDETZA) | |||||||||||||
Full Title: Feasibility, potential efficacy and safety of autologous platelet-rich plasma in the treatment of vascular venous ulcers in Primary Care (phase I and II pilot study) | |||||||||||||
Medical condition: Patients with venous ulcers, aged 40 to 80 years old, registered in five different health centres will be studied. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003637-41 | Sponsor Protocol Number: BIOEU001.00 | Start Date*: 2005-10-26 |
Sponsor Name:Biopure Corporation | ||
Full Title: A Phase II, Multi-Center, Single-Blinded, Placebo-Controlled Study to Evaluate the Safety and Feasibility of Hemoglobin-Based Oxygen Carrier-201 (HBOC-201, hemoglobin-glutamer-250 (bovine)]) on Wo... | ||
Medical condition: Wound Healing in Patients with Peripheral Vascular Disease and Who are Undergoing a Lower Limb Amputation due to Critical Lower Limb Ischemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002520-16 | Sponsor Protocol Number: 626 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:Universitätsklinik für klinische Pharmakologie, Medizinische Universität Wien | |||||||||||||
Full Title: The effects of post-conditioning and administration of Vitamin C on intramuscular high energy phosphate levels | |||||||||||||
Medical condition: ischemia reperfusion injury | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006174-47 | Sponsor Protocol Number: FC-004 | Start Date*: 2012-06-08 | |||||||||||
Sponsor Name:ProFibrix BV | |||||||||||||
Full Title: A Phase 3, Randomized, Single-Blind, Controlled Trial of Topical Fibrocaps™ in Intraoperative Surgical Haemostasis | |||||||||||||
Medical condition: Intraoperative Surgical Hemostasis (Spinal Surgery, Vascular Surgery, Hepatic resection, Soft tissue dissection) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) NL (Completed) GB (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2018-003453-16 | Sponsor Protocol Number: SHP677-304 | Start Date*: 2019-07-31 | |||||||||||
Sponsor Name:Baxalta Innovations GmbH | |||||||||||||
Full Title: A PHASE 3B, PROSPECTIVE, OPEN-LABEL, UNCONTROLLED, MULTICENTER STUDY ON LONGTERM SAFETY AND EFFICACY OF rVWF IN PEDIATRIC AND ADULT SUBJECTS WITH SEVERE VON WILLEBRAND DISEASE (VWD) | |||||||||||||
Medical condition: severe von Willebrand Disease | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) NL (Completed) DE (Completed) ES (Completed) AT (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004227-17 | Sponsor Protocol Number: 2020-53 | Start Date*: 2022-02-24 |
Sponsor Name:ASSISTANCE PUBLIQUE HOPITAUX DE MARSEILLE | ||
Full Title: INNOVATIVE TREATMENT OF SCARRED VOCAL FOLDS BY LOCAL INJECTION OF AUTOLOGOUS ADIPOSE-DERIVED STROMAL VASCULAR FRACTION: EFFICACY VERSUS PLACEBO | ||
Medical condition: Vocal fold scars | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
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