140 result(s) found for: Midazolam.
Displaying page 1 of 7.
| EudraCT Number: 2014-003269-46 | Sponsor Protocol Number: PedMicMida | Start Date*: 2015-04-02 |
| Sponsor Name:Erasmus MC - Sophia | ||
| Full Title: Pediatric microdosing midazolam: elucidating age-related changes in oral drug absorption | ||
| Medical condition: Age-related changes in drug absorption and metabolism in children | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-003293-93 | Sponsor Protocol Number: 14072011 | Start Date*: 2011-09-23 |
| Sponsor Name:Sint Antonius Ziekenhuis | ||
| Full Title: Cyp3A4 metabolism before and after surgery induced weight loss in morbidly obese patients, using midazolam as a model drug | ||
| Medical condition: Morbid obesity | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004958-34 | Sponsor Protocol Number: UNOLE0457 | Start Date*: 2015-01-30 |
| Sponsor Name:University of Leicester | ||
| Full Title: Midazolam Measurement and Modelling using Matrix Samplers | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-004789-36 | Sponsor Protocol Number: 173-01 | Start Date*: 2022-06-29 |
| Sponsor Name:Universität Heidelberg | ||
| Full Title: Randomized, controlled trial of the use of intranasal midazolam for the treatment of terminal agitation in palliative care patients | ||
| Medical condition: Terminal agitation in the final phase | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000026-54 | Sponsor Protocol Number: 18662008 | Start Date*: 2018-09-12 |
| Sponsor Name:Medicinkliniken, Sjukhuset Lidköping | ||
| Full Title: A comparison of sedatives used during gastroscopy, alfentanil vs midazolam | ||
| Medical condition: Sedative effect during gastroscopy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002242-20 | Sponsor Protocol Number: ENT1 | Start Date*: 2013-02-04 |
| Sponsor Name:Royal Bournemouth & Christchurch Hospitals NHS Foundation Trust | ||
| Full Title: A single-centre, randomised controlled study of Entonox versus midazolam in upper GI endoscopy. | ||
| Medical condition: Any patient with symptoms requiring investigation with a gastroscopy. There is no single condition to which this would apply. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-006031-50 | Sponsor Protocol Number: 3005013 | Start Date*: 2007-04-24 | |||||||||||
| Sponsor Name:Orion Corporation Orion Pharma | |||||||||||||
| Full Title: A PROSPECTIVE, MULTI-CENTRE, RANDOMISED, DOUBLE-BLIND COMPARISON OF INTRAVENOUS DEXMEDETOMIDINE WITH MIDAZOLAM FOR CONTINUOUS SEDATION OF VENTILATED PATIENTS IN INTENSIVE CARE UNIT | |||||||||||||
| Medical condition: Patients requiring mechanical ventilation and sedation in ICU. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) GB (Completed) BE (Completed) NL (Completed) DE (Completed) FR (Completed) EE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005215-42 | Sponsor Protocol Number: KloMid02 | Start Date*: 2013-04-12 |
| Sponsor Name:Department of Anesthesiology and Intensive Care Medicine | ||
| Full Title: Children's mood/anxiety, pain, nausea and behavioral changes after premedication with Clonidine versus Midazolam in ENT day surgery. | ||
| Medical condition: Preanesthetic Medication at ear-nose-throat surgery | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-012808-11 | Sponsor Protocol Number: MID001 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Therakind Limited | |||||||||||||
| Full Title: An open label, single dose, pharmacokinetic study of oromucosal midazolam administered to children from 3 months to less than 18 years undergoing routine elective surgery | |||||||||||||
| Medical condition: In the context of the trial, the IMP is to be used as anaesthetic premedication in children undergoing elective routine surgery. (The medical condition for marketing is acute seizures in children ... | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-004480-31 | Sponsor Protocol Number: PSIKET_001CZE | Start Date*: 2020-07-14 |
| Sponsor Name:Národní ústav duševního zdraví | ||
| Full Title: Psilocybin versus ketamine – fast acting antidepressant strategies in treatment-resistant depression | ||
| Medical condition: The study will include 60 patients with pharmaco-resistant depression (30 male, 30 female, aged 18–65). The basic inclusion criterion is the diagnosis of pharmaco-resistant moderate to severe depre... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: CZ (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003582-24 | Sponsor Protocol Number: CLON01 | Start Date*: 2015-06-15 | |||||||||||
| Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
| Full Title: A double blind, randomised, multicentre, active controlled, parallel-group, phase III trial to evaluate the efficacy, safety and pharmacokinetics of intravenous clonidine (hydrochloride) compared t... | |||||||||||||
| Medical condition: sedation in intensive care | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) DE (Prematurely Ended) SE (Completed) IT (Prematurely Ended) CZ (Completed) EE (Prematurely Ended) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-002428-17 | Sponsor Protocol Number: 2013052044 | Start Date*: 2013-10-04 | |||||||||||
| Sponsor Name:Gastroenheden D, Herlev Hospital | |||||||||||||
| Full Title: Nurse Administered Propofol Sedation vs combined sedation with midazolam/fentanil for colonoscopy in patients with IBD. A randomised controlled trial of satisfaction and adhearence to treatment pro... | |||||||||||||
| Medical condition: Satisfaction with sedation during colonoscopy in patients with inflammatory bowel disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-004555-79 | Sponsor Protocol Number: 16-115 | Start Date*: 2017-08-08 |
| Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
| Full Title: Impact of preoperative midazolam on outcome of elderly patients: a multicenter randomised controlled trial | ||
| Medical condition: Under investigation are elderly patients (≥65 years of age) undergoing each kind of surgery with planned general or combined regional and general anaesthesia. Primary, we will investigate the posto... | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003381-21 | Sponsor Protocol Number: RAFAEL | Start Date*: 2023-09-11 |
| Sponsor Name:Psyon, s.r.o. | ||
| Full Title: Regression of atherosclerosis induced by life changing experience with psilocybin | ||
| Medical condition: Ischemic Heart Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-003216-23 | Sponsor Protocol Number: UF8736 | Start Date*: Information not available in EudraCT |
| Sponsor Name:CHRU MONTPELLIER | ||
| Full Title: Intranasal Midazolam versus intranasal Ketamine to sedate newborns for intubation in delivery room | ||
| Medical condition: Maladie des membranes hyalines du nouveau-né (Code CIM : P22.OX-001) | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004890-26 | Sponsor Protocol Number: R0115 | Start Date*: 2005-01-07 |
| Sponsor Name:HULL AND EAST YORKSHIRE NHS TRUST | ||
| Full Title: RANDOMISED CONTROLLED TRIAL OF SEDATION FOR COLONOSCOPY-ENTONOX VERSUS MIDAZOLAM/ FENTANYL | ||
| Medical condition: COLONOSCOPY | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-002106-19 | Sponsor Protocol Number: | Start Date*: 2008-07-10 |
| Sponsor Name:Chelsea & Westminster NHS Foundation Trust | ||
| Full Title: Remifentanil sedation for outpatient endoscopic procedures | ||
| Medical condition: We are investigating the use of remifentanil for sedation in outpatient endoscopic procedures. It will be compared to 'current practice' sedation with midazolam and fentanyl. Patient who are due to... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-001814-34 | Sponsor Protocol Number: OPI 04/006 | Start Date*: 2006-09-12 |
| Sponsor Name:The Norwegian University of Science and Technology | ||
| Full Title: Effects of hypothermia on the disposition of morphine, fentanyl, midazolam and propofol in intensive care unit patients | ||
| Medical condition: Patients treated with therapeutic hypothermia (33-34 °C) and a control group of normothermic patients matched on sex, age and duration of morphine infusion. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002782-37 | Sponsor Protocol Number: ENT05 | Start Date*: 2005-11-17 |
| Sponsor Name:Heart of England NHS Foundation Trust | ||
| Full Title: A Randomised Trial of Inhaled Entonox Plus Local Anaesthesia Versus Intravenous Midazolam Plus Local Anaesthesia To Improve Pain Control During Bone Marrow Biopsy | ||
| Medical condition: This study will involve a group of patients requiring diagnostic bone marrow aspiration and biopsy. The reasons for these will include haematological abnormalities of the blood count , which may be... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003307-20 | Sponsor Protocol Number: SPICEIII | Start Date*: 2014-11-06 |
| Sponsor Name:ANZIC RESEARCH CENTRE | ||
| Full Title: "Sedation Practices in Intensive Care Evaluation: SPICE III – A Prospective Multicentre Randomised Controlled Trial of Early Goal Direct Sedation vs. Standard Care Sedation” | ||
| Medical condition: adult patients hospitalized in intensive therapy unit undergoing continuous and immediate sedation for at least 24 hours | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Ongoing) | ||
| Trial results: (No results available) | ||
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