- Trials with a EudraCT protocol (76)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
76 result(s) found for: Umbilical Cord Blood.
Displaying page 1 of 4.
| EudraCT Number: 2020-005717-40 | Sponsor Protocol Number: 2001-FIVI-002-IC | Start Date*: 2021-05-05 |
| Sponsor Name:IVI Foundation | ||
| Full Title: Umbilical cord plasma for treating endometrial pathologies (thin endometrium / Ash erman’s syndrome/ endometria atrophy) | ||
| Medical condition: Endometrial pathologies (Thin endometrium/ Asherman's syndrome/ Endometrial atrophy) | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-007694-23 | Sponsor Protocol Number: 593 | Start Date*: 2008-07-28 |
| Sponsor Name:Forschergruppe Diabetes e. V. | ||
| Full Title: Transfusion of Autologous Umbilical Cord Blood to Reverse Hyperglycemia in Children with Type 1 Diabetes - A Pilot Study | ||
| Medical condition: Type 1 Diabetes | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001654-15 | Sponsor Protocol Number: NL53018.015.15 | Start Date*: 2015-10-15 |
| Sponsor Name:Máxima Medisch Centrum | ||
| Full Title: Intrauterine resuscitation during term labor by maternal hyperoxygenation. | ||
| Medical condition: Fetal distress during the second stage of labor. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001450-22 | Sponsor Protocol Number: MESCEL-COVID19 | Start Date*: 2020-04-29 | |||||||||||
| Sponsor Name:Fundación de Investigación del Hospital Infantil Universitario Niño Jesús | |||||||||||||
| Full Title: Phase II Clinical Trial to explore the efficacy of allogeneic mesenchymal cells from umbilical cord tissue in patients with severe pulmonary involvement by COVID-19. | |||||||||||||
| Medical condition: Severe pulmonary involvement by COVID-19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003182-34 | Sponsor Protocol Number: 2018-10 | Start Date*: 2018-10-18 |
| Sponsor Name:CHR d'ORLEANS | ||
| Full Title: Randomized, double-blind, controlled clinical trial for comparison of continuous phenylephrine versus norepinephrine infusion for maintenance of hemodynamic stability during cesarean section under... | ||
| Medical condition: hypotension during caesarean section under spinal anesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-006103-35 | Sponsor Protocol Number: SJ-271 | Start Date*: 2012-01-30 | |||||||||||
| Sponsor Name:Næstved hospital | |||||||||||||
| Full Title: The Oxygenation of the Brain DUring elective Caesarean section. A comparison of ephedrine versus phenylephrine | |||||||||||||
| Medical condition: Elective ceasarean section | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-000103-16 | Sponsor Protocol Number: RC13_0008 | Start Date*: 2013-06-21 | ||||||||||||||||
| Sponsor Name:CHU de Nantes | ||||||||||||||||||
| Full Title: Antifungal prophylaxis with Micafungin after cord blood allogeneic stem cell transplantation. | ||||||||||||||||||
| Medical condition: Adult patients receiving allo-Stem Cell Transplantation using Cord Blood as source of stem cells | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-002383-13 | Sponsor Protocol Number: Cord_Blood_Expansion_(SR-1) | Start Date*: 2016-10-18 | |||||||||||
| Sponsor Name:Erasmus MC | |||||||||||||
| Full Title: Umbilical cord blood transplantation in high-risk hematological patients using stemregenin-1 expanded hematopoietic stem cells. A feasibility study focussing on engraftment and hematopoietic recov... | |||||||||||||
| Medical condition: Patients with high-risk hematological diseases, who need a allogeneic stem cell transplantation but who lack a matched unrelated donor | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-011817-26 | Sponsor Protocol Number: BHS-UCB2009 | Start Date*: 2010-10-21 |
| Sponsor Name:UZ Brussel VUB | ||
| Full Title: A pilot study to assess the feasibility of unrelated umbilical cord blood transplantation with coinfusion of third-party mesenchymal stem cells after myeloablative or nonmyeloablative conditioning ... | ||
| Medical condition: Adult patients with hematological malignancies | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000903-10 | Sponsor Protocol Number: 26022016 | Start Date*: 2017-01-04 |
| Sponsor Name:Oulu University Hospital | ||
| Full Title: Efficacy and blood concentrations of epidural hydromorphone in labour | ||
| Medical condition: Labour pain | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000704-28 | Sponsor Protocol Number: GCP#05.01.020 | Start Date*: 2016-06-16 | ||||||||||||||||||||||||||
| Sponsor Name:Gamida Cell Ltd | ||||||||||||||||||||||||||||
| Full Title: A Multicenter, Randomized, Phase III Registration Trial of Transplantation of NiCord®, Ex Vivo Expanded, Umbilical Cord Blood-derived, Stem and Progenitor Cells, versus Unmanipulated Umbilical Cord... | ||||||||||||||||||||||||||||
| Medical condition: High risk haematological malignancies | ||||||||||||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Completed) NL (Completed) GB (GB - no longer in EU/EEA) IT (Prematurely Ended) PT (Completed) FR (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2016-001841-23 | Sponsor Protocol Number: I.2016.010 | Start Date*: 2016-11-16 | |||||||||||
| Sponsor Name:Banc de Sang i Teixits | |||||||||||||
| Full Title: A multicenter, randomized, open-label, two-arms phase I/II clinical trial to asses efficacy and safety of cord blood eye drops in neurotrophic keratopathy | |||||||||||||
| Medical condition: Neurotrophic Keratitis, stage 2 or 3 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019529-33 | Sponsor Protocol Number: 31051970 | Start Date*: 2011-11-21 |
| Sponsor Name:UMCU | ||
| Full Title: A Phase l/ll study to assess safety of co-infusion of haematopoietic stem cells from a haplo-identical donor and a single unit unrelated cord blood in high risk patients | ||
| Medical condition: All patients (0-65y) with a malignancy qualifying for allogenic hematopoietic stem cell transplantation (HSCT) who either (and/or) - are not eligible to other ongoing allo-HSCT protocols, because o... | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-005786-23 | Sponsor Protocol Number: XCEL-SCI-01 | Start Date*: 2016-04-20 | |||||||||||
| Sponsor Name:Banc de Sang i Teixits | |||||||||||||
| Full Title: A phase I/IIa, randomized, double-blind, single-dose, placebo controlled, two-way crossover clinical trial to assess the safety and to obtain efficacy data in intrathecal administration of expanded... | |||||||||||||
| Medical condition: Chronic traumatic spinal cord injury | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-003845-41 | Sponsor Protocol Number: UCL/07/131 | Start Date*: 2009-02-06 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Transplantation of umbilical cord blood (UCB) from unrelated donors (URD) in patients with haematological diseases using a reduced intensity conditioning regimen. | |||||||||||||
| Medical condition: Haematological disorders | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011818-21 | Sponsor Protocol Number: UCL/09/0128 | Start Date*: 2010-06-28 | |||||||||||
| Sponsor Name:University College London [...] | |||||||||||||
| Full Title: Transplantation of umbilical cord blood from unrelated donors in patients with haematological diseases using a myeloablative conditioning regimen | |||||||||||||
| Medical condition: Haematological disorders | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-006632-67 | Sponsor Protocol Number: CHUBX2021/36 | Start Date*: 2022-03-14 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Alkalinization of adrenalized lidocaine in extending epidural analgesia for extremely urgent cesarean section during labor: a randomized controlled trial. | |||||||||||||
| Medical condition: epidural analgesia for extremely urgent cesarean | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000510-22 | Sponsor Protocol Number: 1-2014.4 | Start Date*: 2015-07-28 | |||||||||||
| Sponsor Name:Banc de Sang i Teixits | |||||||||||||
| Full Title: CLINICAL EFFICACY OF PLATELET GEL FROM CORD BLOOD FOR THE TREATMENT OF DIABETIC FOOT ULCERS | |||||||||||||
| Medical condition: Diabetic foot ulcers | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001188-55 | Sponsor Protocol Number: HOVON115 | Start Date*: 2012-07-10 | |||||||||||
| Sponsor Name:HOVON Foundation | |||||||||||||
| Full Title: Double umbilical cord blood transplantation in high-risk hematological patients. A phase II study focussing on the mechanism of graft predominance | |||||||||||||
| Medical condition: Patients with high-risk hematological diseases, who need a allogeneic stem cell transplantation but who lack a matched unrelated donor | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-001956-40 | Sponsor Protocol Number: PK_pregnancy | Start Date*: 2023-03-05 |
| Sponsor Name:Medical University Vienna | ||
| Full Title: Antibiotic pharmacokinetics in women with twin pregnancy | ||
| Medical condition: The target population are twin pregnancy women that will deliver through c-section and that are receiving one or more of the included antibiotics. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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