- Trials with a EudraCT protocol (90)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
90 result(s) found for: Patient-controlled analgesia.
Displaying page 1 of 5.
EudraCT Number: 2007-000808-32 | Sponsor Protocol Number: 1.5 | Start Date*: 2007-09-19 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: A comparison of remifentanil patient-controlled analgesia with epidural analgesia during labor | |||||||||||||
Medical condition: laborpain | |||||||||||||
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Population Age: Adults | Gender: | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006846-24 | Sponsor Protocol Number: HTA074801 | Start Date*: 2009-02-27 |
Sponsor Name:North West London Hospitals NHS Trust | ||
Full Title: An Evaluation of the Effectiveness of Ibuprofen and Morphine for Acute Pain in Sickle Cell Disease | ||
Medical condition: Sickle Cell Disease | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-006203-39 | Sponsor Protocol Number: 3186 | Start Date*: 2006-09-30 |
Sponsor Name: | ||
Full Title: Efficacy of Patient Controlled Paravertebral Analgesia for postoperative analgesia: a comparison of two regimens. | ||
Medical condition: we are investigating the efficacy of patient controlled paravertebral anaesthesia in the post-operative pain control of patients undergoing breast surgery. Therefore the medical condition is post o... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004088-19 | Sponsor Protocol Number: TCI-PCA-002 | Start Date*: 2014-12-12 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Postoperative pain treatment after elective cardiac surgery using patient-controlled target-controlled infusion (TCI-PCA) with hydromorphone vs. patient-controlled analgesia (PCA) with morphine | |||||||||||||
Medical condition: Postoperative pain treatment after elective cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001499-73 | Sponsor Protocol Number: GDW04/2014Amendment1 | Start Date*: 2014-07-31 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: Transversus abdominis plane blok, continous systemic administration of lidocain and patient controlled intravenous morphine - 3 methods for postoperative pain control after laparoscopic colorectal ... | |||||||||||||
Medical condition: postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005264-98 | Sponsor Protocol Number: GDW112012 | Start Date*: 2013-05-06 | |||||||||||
Sponsor Name:University hospitals Leuven | |||||||||||||
Full Title: A comparison between continuous systemic Lidocain and patient controlled intravenous morphine administration for pain control after posterior spinal fusion (PSF) in adolescent idiopatic scoliosis (... | |||||||||||||
Medical condition: postoperative pain | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003648-31 | Sponsor Protocol Number: PKPDHM-001 | Start Date*: 2011-11-17 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Pharmacokinetic-pharmacodynamic modeling of the postoperative pain sensation during patient-controlled analgesia with target-controlled infusion of Hydromorphone, taking into account the interactio... | |||||||||||||
Medical condition: Pain therapy after elective cardiac surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004600-30 | Sponsor Protocol Number: mvdv/er102015 | Start Date*: 2016-01-18 |
Sponsor Name:University Hospitals Leuven | ||
Full Title: Conventional patient controlled epidural analgesia (PCEA) versus programmed intermittent epidural boluses (PIEB) for labor analgesia: a randomized, double blind study in nulliparous women | ||
Medical condition: providing adequate analgesia during labor and child birth | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-001232-59 | Sponsor Protocol Number: AGO/2019/002 | Start Date*: 2020-01-29 | |||||||||||
Sponsor Name:Ghent University Hospital | |||||||||||||
Full Title: Safety and Efficacy of Patient Controlled Analgesia using the Sublingual Sufentanil Tablet System (SSTS) in a fast track rehabilitation program after Total Knee Arthroplasty. | |||||||||||||
Medical condition: Total Knee Arthroplasty | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000130-19 | Sponsor Protocol Number: PHANOS2012 | Start Date*: 2012-08-30 | |||||||||||
Sponsor Name:Medizinische Universität Graz, Univ. Klinik für Anästhesiologie und Intensivmedizin, Abt. Anästhesie und Intensivmedizin | |||||||||||||
Full Title: PHANOS (PHysostigmine-enHAnced Opioid analgeSia) study | |||||||||||||
Medical condition: Postoperative pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007322-19 | Sponsor Protocol Number: RPC190 | Start Date*: 2009-07-07 |
Sponsor Name:Queen Victoria Hospital NHS Foundation Trust | ||
Full Title: A Comparison of Remifentanil Patient-Controlled Analgesia vs. Oral Morphine Analgesia for Dressing Changes in Burns Patients. | ||
Medical condition: Pain experienced by patients with pre-existing burns presenting to the burns outpatients unit requiring two or more dressing changes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023754-37 | Sponsor Protocol Number: 2010JTW01 | Start Date*: 2011-01-28 |
Sponsor Name:Ashford and St Peters Hospitals NHS Trust | ||
Full Title: Local Anaesthetic Infusion for Laparoscopic Hysterectomy: A Randomised controlled trial | ||
Medical condition: women having a total laparoscopic or vaginally assisted laparoscopic hysterectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003319-76 | Sponsor Protocol Number: MVDV/ER082019 | Start Date*: 2019-10-09 |
Sponsor Name:Univerity Hospitals Leuven | ||
Full Title: High volume PCEA versus PIEB for labor analgesia: a randomized, double-blind multicenter non-inferiority study in nulliparous women. | ||
Medical condition: providing adequate analgesia during child birth | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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 (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002978-62 | Sponsor Protocol Number: 2007/13 | Start Date*: 2009-03-18 | ||||||||||||||||
Sponsor Name:Hopital Foch | ||||||||||||||||||
Full Title: Influence de l’analgésie peropératoire (sufentanil administré selon les critères usuels ou rémifentanil administré par un système automatisé à partir de l’Index Bispectral) sur la consommation de m... | ||||||||||||||||||
Medical condition: general anesthesia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004696-24 | Sponsor Protocol Number: ANESBUPI_1/2014 | Start Date*: 2016-02-29 |
Sponsor Name:HOSPITAL UNIVERSITARIO LA PAZ, SERVICIO DE ANESTESIA | ||
Full Title: Breakthrough pain incidence in pregnant women comparing two Epidural analgesia shemes added to a continuous infusion (bowling planned indicators and analgesia epidural patient controlled): double-b... | ||
Medical condition: EPIDURAL ANALGESIA IN PARTURIENTS | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-014362-25 | Sponsor Protocol Number: VDV07/09 | Start Date*: 2009-10-21 |
Sponsor Name:Marc Van de Velde | ||
Full Title: Onderhoud van de analgesie tijdens de arbeid na gecombineerde spinale epidurale anesthesie: ”positieve invloed op kwaliteit van analgesie door patient-controlled epidural analgesia met clonidine en... | ||
Medical condition: Combined spinal -epidural analgesia during labour. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-005518-11 | Sponsor Protocol Number: 2006-10 | Start Date*: 2007-01-24 |
Sponsor Name:Örebro University Hospital | ||
Full Title: Epidural analgesia or opatient controlled regional analgesia for radical Retropubic Prostatectomy. A randomized, double-blind study. | ||
Medical condition: Postoperative pain after radical retropubic prostatectomy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000202-75 | Sponsor Protocol Number: P.Sitsen.03 | Start Date*: 2007-06-15 |
Sponsor Name:Leids Universitair Medisch Centrum | ||
Full Title: A comparison of the efficacy of levobupivacaine 0,125%, ropivacaine 0,125% and ropivacaine 0,2%, all combined with sufentanil 0.5 micrograms/mL, in patient-controlled epidural analgesia after hyste... | ||
Medical condition: Primary Objective •to compare the analgesic efficacy of levobupivacaine and ropivacaine in patient-controlled epidural analgesia, as assessed by the number of requests for epidural bolus injections... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000235-27 | Sponsor Protocol Number: S-20120216 | Start Date*: 2013-02-19 | |||||||||||
Sponsor Name:Odense universitets Hospital | |||||||||||||
Full Title: Interscalener blockade for surgery on the shoulder, a comparison of two dosing regimens: Fixed intermittent bolus with the possibility of PCA (Patient controlled administration) Vs. continuous infu... | |||||||||||||
Medical condition: Shoulder frcture Rotator cuff leasion Shoulder alluplastic | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
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