- Trials with a EudraCT protocol (240)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (37)
240 result(s) found for: Propofol.
Displaying page 1 of 12.
| EudraCT Number: 2005-005400-17 | Sponsor Protocol Number: 2005-087 | Start Date*: 2005-12-15 |
| Sponsor Name:Dept. of Anaesthesia, Center of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet | ||
| Full Title: Optimizing propofol in obese patients | ||
| Medical condition: Depth of anesthesia during hysterescomia in propofol/remifentanil anaesthesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-000537-69 | Sponsor Protocol Number: PROP2% | Start Date*: 2015-09-21 |
| Sponsor Name:Universitair Ziekenhuis Brussel | ||
| Full Title: Real time monitoring of blood propofol concentration | ||
| Medical condition: - General anaesthesia - Pharmacokinetics and Pharmacodynamics of Propofol - Inflammatory parameters - Elective thyroid, oncologic breast,ENT or cervical arthrodesis surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004551-67 | Sponsor Protocol Number: SED001 | Start Date*: 2017-04-18 |
| Sponsor Name:Sedana Medical AB | ||
| Full Title: A randomised, controlled, open-label study to confirm the efficacy and safety of sedation with isoflurane in invasively ventilated ICU patients using the AnaConDa administration system | ||
| Medical condition: Adult subjects admitted to the ICU clinically indicated to require sedation with propofol and invasive ventilation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) SI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000958-56 | Sponsor Protocol Number: 2019/375 | Start Date*: 2019-08-16 |
| Sponsor Name:Helse Fonna | ||
| Full Title: “Haemodynamic stability during induction of general anesthesia with propofol and remifentanil: A randomized, controlled, double-blind study comparing low vs high propofol doses.” | ||
| Medical condition: In daily clinical work we observe a hypotensive effect and a reduction in HR when induction of general anesthesia is performed using propofol and remifentanil. It is difficult to differentiate the ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002323-28 | Sponsor Protocol Number: prop01 | Start Date*: 2016-06-28 |
| Sponsor Name:Universitair Ziekenhuis Brussel | ||
| Full Title: Blood concentration and pharmacokinetic analysis of propofol following administration of single induction dose in small children | ||
| Medical condition: Children scheduled for elective surgery | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001373-33 | Sponsor Protocol Number: 2016-3 | Start Date*: 2017-02-17 |
| Sponsor Name:Region Ostergotland | ||
| Full Title: Clinical Study Protocol An open phase IV,RCT, evaluating patient controlled sedation, in three different dosages of propofol in healthy subjects undergoing elective gynaecological out-patient su... | ||
| Medical condition: Gynecological outpatient surgery | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001770-15 | Sponsor Protocol Number: 1418 | Start Date*: 2020-01-24 |
| Sponsor Name:Complejo Asistencial Universitario de León | ||
| Full Title: Analysis of the effectiveness of Non-painful Endovenous Management (MENA) in the administration of Propofol | ||
| Medical condition: Propofol is used as an intravenous agent for induction and anesthetic maintenance. However, without any intervention before your administration, as is usually administered, the incidence of local p... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002780-14 | Sponsor Protocol Number: Asena/Prop-01 | Start Date*: 2007-07-16 |
| Sponsor Name:Hospital General Universitario Alicante, Dpto Farmacologia Clinica | ||
| Full Title: Estudio comparativo de la eficacia de la bomba de jeringa Alaris® (Asena®) de uso polivalente en la administración de tres formulaciones de propofol | ||
| Medical condition: inducción anestésica en pacientes que requieren cirugía CLASS ASA I y II | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003909-26 | Sponsor Protocol Number: BOP-TCI-001 | Start Date*: 2014-02-04 |
| Sponsor Name:UMCG | ||
| Full Title: Bayesian optimized Propofol Target-Controlled Infusion | ||
| Medical condition: Patients requiring general anaesthesia for surgery using propofol and requiring an arterial line for invasive blood pressure monitoring as part of their clinical care. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-003571-39 | Sponsor Protocol Number: HC-G-H-0705 | Start Date*: 2008-04-23 |
| Sponsor Name:B. Braun Melsungen AG | ||
| Full Title: Prospective, monocentric, controlled, randomized, double-blind study to compare two different propofol emulsions regarding tolerability and injection pain during the induction of anesthesia in adults | ||
| Medical condition: reduction of injection pain during induction of anaesthesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-018233-21 | Sponsor Protocol Number: WEC 0910 | Start Date*: 2010-03-31 |
| Sponsor Name:Leiden University Medical Centre | ||
| Full Title: Modeling the respiratory effects of subanesthetic doses of propofol under closed-loop or non-steady-state conditions without and with a remifentanil background infusion in healthy volunteers. | ||
| Medical condition: This study is performed in healthy volunteers. The study is aimed at investigating the effect of propofol and remifentanil-propofol interaction on breathing in awake, non-artificially ventilated vo... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000022-29 | Sponsor Protocol Number: 013/2011 | Start Date*: 2011-09-21 |
| Sponsor Name:Medizinische Universität Wien | ||
| Full Title: The interaction of intravenous lidocaine on the Cp50 of propofol for skin incision | ||
| Medical condition: the effects of intravenous application of lidocaine on the Cp50 during propofol narcosis should be investigated | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002533-10 | Sponsor Protocol Number: SuRe-001 | Start Date*: 2013-05-22 |
| Sponsor Name:UMCG | ||
| Full Title: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil’ | ||
| Medical condition: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-000964-33 | Sponsor Protocol Number: Feline02 | Start Date*: 2015-09-17 |
| Sponsor Name:Erasmus Medical Center, Department of Anesthesiology | ||
| Full Title: Dexmedetomidine versus propofol in awake implantation of a neuromodulative system. | ||
| Medical condition: Awake implantation of a neuromodulative system. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-010614-30 | Sponsor Protocol Number: CH/2007/2746 | Start Date*: 2009-05-08 |
| Sponsor Name:University Hospitals Bristol | ||
| Full Title: Randomised cross-over pilot study to determine the effects of isoflurane and propofol on pulmonary vascular resistance in children with pulmoanry hypertension | ||
| Medical condition: children with pulmonary hypertension | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000584-25 | Sponsor Protocol Number: FLAM01 | Start Date*: 2012-03-29 |
| Sponsor Name:UZBrussel | ||
| Full Title: Propofol and etomidate. Are they also safe for patients with Brugada-Syndrome? | ||
| Medical condition: Patients suspected to have Brugada Syndrome | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-017921-20 | Sponsor Protocol Number: none | Start Date*: 2010-09-16 |
| Sponsor Name:Univ. Klinik für Anästhesiologie | ||
| Full Title: Influence of Gender on the Plasma-Effect site equilibration time of propofol anesthetic and Cisatracurium Besylate neuromuscular blocking agent. A pilot study. | ||
| Medical condition: effect of Gender on Pharmacokinetics of Propofol and cisatracurium | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003737-19 | Sponsor Protocol Number: CHUB-ITF-sevo-propofol | Start Date*: 2023-01-10 |
| Sponsor Name:CHU Brugmann | ||
| Full Title: Influence of sevoflurane and propofol on maximum muscular strength, speed of contraction and relaxation, in humans: A pilot study. | ||
| Medical condition: Impact of anesthetic drugs on neuromuscular transmission | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000071-90 | Sponsor Protocol Number: AGO/2017/002 | Start Date*: 2017-03-15 |
| Sponsor Name:Ghent University Hospital | ||
| Full Title: Effect of sevoflurane and propofol on hepato-splanchnic pressure and flow during hepatobiliary surgery. | ||
| Medical condition: patients scheduled for hepato-biliary surgery. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-004455-78 | Sponsor Protocol Number: SINUS | Start Date*: 2017-06-09 |
| Sponsor Name:Region Östergötland | ||
| Full Title: Sedation with propofol and remifentanil during ventricular tachycardia treatment: patient-controlled versus nurse anesthetists controlled - a randomized controlled trial | ||
| Medical condition: Percutaneous pericardial access for mapping and ablation of ventricular tachycardia | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
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