- Trials with a EudraCT protocol (89)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (15)
89 result(s) found for: Clonidine.
Displaying page 1 of 5.
| EudraCT Number: 2015-001699-23 | Sponsor Protocol Number: Clonkin1 | Start Date*: 2015-12-01 |
| Sponsor Name:Deventer Hospital | ||
| Full Title: Pharmacokinetics and clinical effects of escalating doses of clonidine in ICU patients | ||
| Medical condition: Delirium The pharmacokinetic and dynamic properties of intravenous clonidine in critical ill mechanically treated patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-003678-82 | Sponsor Protocol Number: CHDR0606 | Start Date*: 2007-07-10 | |||||||||||
| Sponsor Name:Centre for Human Drug Research | |||||||||||||
| Full Title: Pharmacokinetics and effects of oral clonidine in children with suspected Growth Hormone deficiency | |||||||||||||
| Medical condition: Clonidine is studied in the paediatric population, more specific children with short stature. It is used as a diagnostic tool to establish Growth Hormone reserve in routine practice. | |||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2013-000815-26 | Sponsor Protocol Number: LUCID | Start Date*: 2013-08-26 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: THE OSLO STUDY OF CLONIDINE IN ELDERLY PATIENTS WITH DELIRIUM | ||
| Medical condition: Delirium in elderly patients admitted to the acute geriatric ward | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-004471-22 | Sponsor Protocol Number: GE 06-2008 | Start Date*: 2008-09-01 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Minimum local anesthetic concentration of levobupivacaine and clonidine given for caudal anesthesia in children | |||||||||||||
| Medical condition: postoperative pain management | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003560-74 | Sponsor Protocol Number: p2011-1 | Start Date*: 2012-09-25 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Effectiveness of Clonidine for the treatment of radicular pain: A randomized, double-blind and prospective study. (EFFOC study) | ||
| Medical condition: Radicular lumbar pain | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-024100-10 | Sponsor Protocol Number: OZR-2010-17 | Start Date*: 2011-03-28 |
| Sponsor Name:The Rotterdam Eye Hospital | ||
| Full Title: Clonidine as an adjuvant to prolong local anaesthesia in ophthalmic surgery with cryocoagulation. A randomized, controlled, patient-masked trial. | ||
| Medical condition: - Rhegmatogenous retinal detachment requiring cryocoagulation and episcleral explant. - Glaucoma requiring cryocoagulation of the ciliary body. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-005512-12 | Sponsor Protocol Number: MVDV | Start Date*: 2007-12-19 |
| Sponsor Name:University Hospitals Leuven | ||
| Full Title: Een verbetering van de analgesie na episiotomie door epidurale toediening van neostigmine en clonidine. | ||
| Medical condition: Combinedn spinal-epidural analgesia during labour. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003008-53 | Sponsor Protocol Number: 80836009820016 | Start Date*: 2014-12-10 |
| Sponsor Name:University Medical Center Utrecht | ||
| Full Title: Clonidine Augmentation Therapy in Schizophrenia | ||
| Medical condition: Schizophrenia, schizophreniform disorder, schizoaffective disorder | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-014870-16 | Sponsor Protocol Number: BA2009-28-01 | Start Date*: 2009-12-10 |
| Sponsor Name:BioAlliance Pharma | ||
| Full Title: A phase II, multicentre, randomized, double-blind, placebo-controlled study comparing the efficacy and safety of Clonidine Lauriad® 50 μg and 100 μg mucoadhesive buccal tablet (MBT) applied once da... | ||
| Medical condition: Prevention and treatment of chemoradion therapy-induced oral mucositis. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) ES (Completed) DE (Completed) HU (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: 2009-011059-27 | Sponsor Protocol Number: RBHP 2009 BONNIN | Start Date*: 2009-06-17 |
| Sponsor Name:CHU Clermont-Ferrand | ||
| Full Title: Etude des effets de l’adjonction de clonidine au mélange anesthésique local + opiacé destiné à l’infusion péridurale autocontrôlée pour l’analgésie du travail obstétrical (lévobupivacaïne 0,568 mg/... | ||
| Medical condition: parturiente en cours de travail obstétrical | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004796-35 | Sponsor Protocol Number: EPICLO2006 | Start Date*: 2007-04-20 |
| Sponsor Name:R&D Department, Box 146, Addenbrooke's Hospital | ||
| Full Title: A study of effect of epidural clonidine on postoperative pain relief, hyperalgesia and chronic pain in patients undergoing colorectal surgery | ||
| Medical condition: 1. Postoperative pain and hyperalgesia following laparotomy for colorectal surgery 2. Chronic pain following laparotomy for colorectal surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-008434-36 | Sponsor Protocol Number: VDV12/08 | Start Date*: 2009-02-12 |
| Sponsor Name:Marc Van de Velde | ||
| Full Title: Een gecombineerde spinale epidurale anesthesie bij arbeid : positieve invloed op kwaliteit van analgesie door epiduraal clonidine en neostigmine bij doorbraakpijn? | ||
| Medical condition: Combined spinal-epidural analgesia during labour | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| 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: 2010-024018-71 | Sponsor Protocol Number: 2010-024018-71 | Start Date*: 2011-03-31 |
| Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | ||
| Full Title: PREMEDICATION IN CHILDREN: CLONIDINE VERSUS MELATONIN | ||
| Medical condition: HEALTHY CHILDREN UNDERGOING ELECTIVE MINOR SURGERY | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: IT (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-000714-74 | Sponsor Protocol Number: 1.0 | Start Date*: 2008-07-15 |
| Sponsor Name:Institution of Paediatric Anaesthesia and intensiv care, Astrid Lindgren Childrens Hospital, Karolin | ||
| Full Title: Premedication in paediatric patients: Dose finding study of clonidine administrated as nasal aerosol. | ||
| Medical condition: Premedication prior to anaesthesia | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-004988-30 | Sponsor Protocol Number: 23386753 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Mater Misercordiae Hospital - Department of Anaesthesia | ||
| Full Title: PHARMACOKINETICS AND ANALGESIC EFFICACY OF LAEVOBUPIVACAINE, FENTANYL AND CLONIDINE FOR POSTOPERATIVE PARAVERTEBRAL ANAESTHESIA. | ||
| Medical condition: We are aiming to provide postoperative analgesia for breast surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: IE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-018781-23 | Sponsor Protocol Number: 2917800009 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Top Institute Food and Nutrition | |||||||||||||
| Full Title: Diagnose of GH-deficiency: comparing the dietary-protein test with conventional Growth Hormone Stimulation Tests | |||||||||||||
| Medical condition: To investigate if there is a correlation between the peak GH concentrations after ingestion of gelatin protein and the peak GH concentrations after the two standard tests (GHST) in order to discrim... | |||||||||||||
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| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004281-18 | Sponsor Protocol Number: NC12547 | Start Date*: 2020-08-18 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Clonidine for Tourniquet-related Pain in Children (CLOTCH) -Study: A Pilot Study | |||||||||||||
| Medical condition: Pain, which occurs in relation to the use of tourniquets during limb surgery. Tourniquets are positioned on the upper part of the limb in question, inflated and thereby stops perfusion of the limb.... | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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