- Trials with a EudraCT protocol (194)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (94)
194 result(s) found for: UZ.
Displaying page 4 of 10.
EudraCT Number: 2014-002830-30 | Sponsor Protocol Number: DDD14JRindi | Start Date*: 2014-12-24 |
Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
Full Title: Supersaturation and precipitation of indinavir in the stomach of healthy human volunteers | ||
Medical condition: Healthy human volunteers (administration of a Protease inhibitor) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001217-16 | Sponsor Protocol Number: AT032012 | Start Date*: 2012-06-05 |
Sponsor Name:UZLeuven | ||
Full Title: Dorsal penile nerve block(DPNB) for circumcision: a comparison of ultrasound-guided vs. landmark technique. | ||
Medical condition: Postoperative pain and recovery after circumcision | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005845-12 | Sponsor Protocol Number: 11/2006 - MVdV | Start Date*: 2007-01-08 |
Sponsor Name:UZ leuven, Marc Van de Velde | ||
Full Title: Combined spinal-epidural anaesthesia during labour : has the epidural administration of clonidine and neostigmine a positive influence on the quality of analgesia ? | ||
Medical condition: combined spinal-epidural analgesia during labour | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-001098-13 | Sponsor Protocol Number: NA | Start Date*: 2008-04-30 |
Sponsor Name:UZ Leuven | ||
Full Title: Simultaneous administration of lorazepam and levetiracetam in non-convulsive status epilepticus, followed by IV valproate: a prospective, randomized, placebo-controled, double-blind pilot trial. | ||
Medical condition: Non-convulsive status epilepticus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003790-34 | Sponsor Protocol Number: DDD17COLSAM | Start Date*: 2018-01-09 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Drug disposition in the human colon: sampling optimization | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-005248-41 | Sponsor Protocol Number: DDD17Fenogal | Start Date*: 2017-05-17 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Influence of gastrointestinal lipid digestion in the absorption of fenofibrate from a lipid-based formulation | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002519-17 | Sponsor Protocol Number: DDD16JRtac | Start Date*: 2016-09-12 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Supersaturation and precipitation of tacrolimus in the stomach of healthy volunteers | ||
Medical condition: Healthy human volunteers , investigation of the drug's supersaturation behaviour in the stomach | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-000297-30 | Sponsor Protocol Number: DDD13PM | Start Date*: 2013-03-21 |
Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
Full Title: The use of the non-absorbable marker paromomycin sulfate for the evaluation of the gastrointestinal transit | ||
Medical condition: healthy volunteers (administration of antibacterial drug) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004629-28 | Sponsor Protocol Number: ANE 08/06 | Start Date*: 2006-10-03 |
Sponsor Name:UZ Leuven | ||
Full Title: Een gecombineerde spinale epidurale anesthesie (CSE) bij arbeid : nood aan een fluid load (colloïden) ? | ||
Medical condition: Combined spinal epidural analgesia during labour : necessity of a fluid load with colloids ? | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-002700-78 | Sponsor Protocol Number: DDD16RITONAVIR | Start Date*: 2016-10-28 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Supersaturation and precipitation of ritonavir in the gastrointestinal tract of healthy volunteers | ||
Medical condition: Healthy human volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004636-29 | Sponsor Protocol Number: DDD13DICLO | Start Date*: 2014-02-04 |
Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
Full Title: Supersaturation and precipitation of diclofenac in the stomach of healthy human volunteers | ||
Medical condition: Healthy human volunteers (administration of a Non-Steroidal Anti-Inflammatory Drug) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-000324-19 | Sponsor Protocol Number: DDDCF14 | Start Date*: 2014-09-18 |
Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
Full Title: Collection and characterization of gastrointestinal fluids in different populations and conditions | ||
Medical condition: healthy human volunteers (administration of a proton-pump inhibitor) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-002593-27 | Sponsor Protocol Number: S64291 | Start Date*: 2022-06-17 |
Sponsor Name:UZ Leuven | ||
Full Title: Budesonide as a treatment for low-grade duodenal inflammation in functional dyspepsia. | ||
Medical condition: Functional dyspepsia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000756-27 | Sponsor Protocol Number: VUB08001 | Start Date*: 2008-06-23 |
Sponsor Name:UZ Brussel | ||
Full Title: Activity of sunitinib in esophageal cancer, melanoma and sarcoma. | ||
Medical condition: Patients with advanced esophageal cancer, melanoma and sarcoma. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005286-24 | Sponsor Protocol Number: 22112015 | Start Date*: 2016-02-24 |
Sponsor Name: | ||
Full Title: Baclofen in managing acute alcohol withdrawal | ||
Medical condition: Alcohol withdrawal syndrome | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003224-19 | Sponsor Protocol Number: CVC-µPL | Start Date*: 2005-10-04 |
Sponsor Name:UZ Leuven - Bloedings- en Vaatziekten | ||
Full Title: Clinical Trial of Microplasmin in Patients with Long-Term Venous Access Catheter Thrombosis | ||
Medical condition: Thrombotic occlusion of central venous access devices | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005114-33 | Sponsor Protocol Number: s57283 | Start Date*: 2015-03-10 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Effectiveness of Botulinum Toxin Infiltration for treatment of upper limb dysfunctions after treatment for breast cancer | |||||||||||||
Medical condition: The aim of this study is to examine the effect of Botolinum Toxine infiltration in the pectoral muscle, in combination with an individual physical therapy programme, on pain and upper limb dysfunct... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002151-10 | Sponsor Protocol Number: NEUROPROTECTpost-CA | Start Date*: 2015-08-07 | |||||||||||
Sponsor Name:UZ Leuven | |||||||||||||
Full Title: Neuroprotective goal directed hemodynamic optimization in post-cardiac arrest patients: a randomized controlled trial (the NEUROPROTECT post-CA trial) | |||||||||||||
Medical condition: post-cardiac arrest patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004671-39 | Sponsor Protocol Number: 2019/318 | Start Date*: 2020-01-28 |
Sponsor Name:Universitair Ziekenhuis Brussel (UZ Brussel) | ||
Full Title: The effect of handheld-multimedia versus midazolam premedication on the level of perioperative anxiety in pediatric day-care. A randomized controlled trial. | ||
Medical condition: Perioperative anxiety in children scheduled for an elective circumcision, dental care or tonsillectomy/adenoidectomy in day-care | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2021-005426-18 | Sponsor Protocol Number: DECONGEST_v1.0 | Start Date*: 2022-03-02 | |||||||||||
Sponsor Name:UZ Brussel | |||||||||||||
Full Title: Diuretic Treatment in Acute Heart Failure with Volume Overload Guided by Serial Spot Urine Sodium Assessment | |||||||||||||
Medical condition: Acute Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
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