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Clinical trials for Fast track

The European Union Clinical Trials Register   allows you to search for protocol and results information on:
  • interventional clinical trials that were approved in the European Union (EU)/European Economic Area (EEA) under the Clinical Trials Directive 2001/20/EC
  • clinical trials conducted outside the EU/EEA that are linked to European paediatric-medicine development

  • EU/EEA interventional clinical trials approved under or transitioned to the Clinical Trial Regulation 536/2014 are publicly accessible through the
    Clinical Trials Information System (CTIS).


    The EU Clinical Trials Register currently displays   44336   clinical trials with a EudraCT protocol, of which   7366   are clinical trials conducted with subjects less than 18 years old.   The register also displays information on   18700   older paediatric trials (in scope of Article 45 of the Paediatric Regulation (EC) No 1901/2006).

    Phase 1 trials conducted solely on adults and that are not part of an agreed paediatric investigation plan (PIP) are not publicly available (see Frequently Asked Questions ).  
     
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    18 result(s) found for: Fast track. Displaying page 1 of 1.
    EudraCT Number: 2013-001008-13 Sponsor Protocol Number: 497 Start Date*: 2013-09-18
    Sponsor Name:Sint Maartenskliniek
    Full Title: Fast-track rehabilitation protocol for Total Knee Arthroplasty: A Randomized Controlled Trial comparing Local Infiltration Analgesia with Femoral Nerve Block
    Medical condition: patients requiring total knee arthroplasty for non-inflammatory osteoarthritis of the knee
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
    EudraCT Number: 2010-021604-16 Sponsor Protocol Number: etoricoxib-fast-track-2010 Start Date*: 2010-12-08
    Sponsor Name:Charité Universitätsmedizin Berlin
    Full Title: A double-blind, randomized, placebo controlled study to evaluate the effectiveness of etoricoxib as an additive analgesic to epidural analgesia in colon or rectum fast-track surgery
    Medical condition: Post-operative pain after laparoscopic colon or rectum surgery in fast-track design
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004865 10036236 Postoperative pain relief LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2011-000698-30 Sponsor Protocol Number: LK10 Start Date*: 2011-04-18
    Sponsor Name:Henrik Kehlet
    Full Title: Postoperative søvnforstyrrelser efter Zolpidem behandling ved fast-track hofte- eller knæalloplastik
    Medical condition: Postoperative REM sleep reduction after fast-track hip and knee arthroplasty. Comparison of preoperative level and level of REM on first postoperative night. The effect of one administration of Zo...
    Disease: Version SOC Term Classification Code Term Level
    14.1 10029205 - Nervous system disorders 10036160 Poor sleep LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2013-004031-71 Sponsor Protocol Number: NL457401.094.13 Start Date*: 2015-01-14
    Sponsor Name:Spaarne Hospital
    Full Title: Local infiltration with anesthetics vs placebo in patients with elective total hip replacement (thr) in fast-track protocol
    Medical condition: primary coxarthrosis
    Disease:
    Population Age: Elderly Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    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
    Disease: Version SOC Term Classification Code Term Level
    21.1 10042613 - Surgical and medical procedures 10036276 Postoperative analgesia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2011-002034-38 Sponsor Protocol Number: THL-04-11 Start Date*: 2011-06-15
    Sponsor Name:Rgshospitalet
    Full Title:
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    13.1 10042613 - Surgical and medical procedures 10036236 Postoperative pain relief LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2017-000180-32 Sponsor Protocol Number: 761 Start Date*: 2017-02-10
    Sponsor Name:Sint Maartenskliniek Nijmegen
    Full Title: Pharmacokinetic Profile of Ropivacaine after Periarticular Local Infiltration Analgesia for Primary Total Knee Arthroplasty Without the use of a Tourniquet.
    Medical condition: patients receiving primary total knee replacement
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-004814-33 Sponsor Protocol Number: MOFA Start Date*: 2006-03-23
    Sponsor Name:Gesellschaft für Wissens- und Technologietransfer
    Full Title: Metabolic optimized fast track concept in general surgery
    Medical condition: Carcinoma of the colon or the liver scheduled for surgical resection
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: View results
    EudraCT Number: 2014-003010-93 Sponsor Protocol Number: 620 Start Date*: 2014-10-15
    Sponsor Name:Sint Maartenskliniek
    Full Title: Pharmacokinetic Profile of Ropivacaïne after Periarticular Local Infiltration Analgesia for Primary Total Knee Arthroplasty
    Medical condition: patients receiving primary total knee replacement
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
    EudraCT Number: 2019-000596-16 Sponsor Protocol Number: DH112018 Start Date*: 2019-04-17
    Sponsor Name:University Hospitals Leuven
    Full Title: Erector spinae plane block for minimal invasive direct coronary artery bypass surgery. A double blind, prospective randomized placebo-controlled trial.
    Medical condition: postoperative pain
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2019-001125-27 Sponsor Protocol Number: DH022019 Start Date*: 2019-06-04
    Sponsor Name:University Hospitals Leuven
    Full Title: Erector Spinae plane block for minimal invasive mitral valve surgery. A double blind, prospective randomized placebo-controlled trial.
    Medical condition: postoperative pain
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2010-022428-58 Sponsor Protocol Number: PRECONII Start Date*: 2010-09-21
    Sponsor Name:Aarhus University Hospital, Skejby
    Full Title: PRECON 2 – Fast-track cardiac surgery (kvalitetssikringsprojekt). Remifentanyl anæstesi til koronar bypass (CABG) med eller uden samtidig udskiftning af aortaklappen (AVR) bedømt ved opvågningsforl...
    Medical condition: Anæstesi til hjertekirurgiske patienter.Studiet er randomiseret med inklusion af patienter til elektiv CABG med/ uden samtidig AVR med anvendelse af cardiopulmonal bypass. Patienter randomiseres ti...
    Disease: Version SOC Term Classification Code Term Level
    12.1 10002092 Anaesthesia and allied procedures HLT
    12.1 10007530 Cardiac complications of anaesthesia or other sedation in labour and delivery LLT
    12.1 10012206 Delayed recovery from anaesthesia LLT
    12.1 10021722 Induction and maintenance anaesthesia LLT
    12.1 10031777 Other complications of anaesthesia or other sedation in labour and delivery LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2010-023095-31 Sponsor Protocol Number: HUM-001 Start Date*: 2012-11-28
    Sponsor Name:Humedics GmbH
    Full Title:
    Medical condition: liver resection
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004848 10024689 Liver function analyses HLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: View results
    EudraCT Number: 2013-001873-25 Sponsor Protocol Number: vers20130714 Start Date*: 2013-08-29
    Sponsor Name:County Council of Östergötland
    Full Title: Will intrathecal analgesia contribute to a faster recovery compared with epidural analgesia after open surgery for gynecological cancer. An open controlled randomized study.
    Medical condition: Recovery after open abdominal surgery for gynecological cancer
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: SE (Completed)
    Trial results: View results
    EudraCT Number: 2012-002572-13 Sponsor Protocol Number: RH-4074-OJ1 Start Date*: 2012-09-17
    Sponsor Name:Henrik Kehlet
    Full Title: Efficacy of midodrine for the prevention of orthostatic hypotension during early mobilization after fast-track hip arthroplasty - a randomized, placebo controlled trial
    Medical condition: Postoperative orthostatic hypotension during early mobilization after fast-track hip arthroplasty
    Disease: Version SOC Term Classification Code Term Level
    14.1 10047065 - Vascular disorders 10021100 Hypotension orthostatic LLT
    14.1 10047065 - Vascular disorders 10021102 Hypotension orthostatic symptomatic LLT
    14.1 10022117 - Injury, poisoning and procedural complications 10050632 Postoperative hypotension LLT
    14.1 10047065 - Vascular disorders 10036433 Postural hypotension LLT
    14.1 10047065 - Vascular disorders 10031127 Orthostatic hypotension PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2016-003906-16 Sponsor Protocol Number: DESEVAR Start Date*: 2017-02-14
    Sponsor Name:Begoña Quintana
    Full Title: FAST-TRACK IN ENDOVASCULAR AORTIC ANEURYSM REPAIR WITH DESFLURANE AND SEVOFLURANE: A RANDOMIZED CLINICAL TRIAL
    Medical condition: AORTIC ANEURYSM
    Disease: Version SOC Term Classification Code Term Level
    19.1 100000004866 10002889 Aortic aneurysms and dissections HLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2019-001859-40 Sponsor Protocol Number: 2019-041 Start Date*: 2020-11-05
    Sponsor Name:Franciscus Gasthuis & Vlietland
    Full Title: PEROPERATIVE TRANEXAMIC ACID IN BARIATRIC FAST TRACK SURGERY TO REDUCE HEMORRAGE RATES
    Medical condition: Morbid obesity
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10059610 Obesity surgery LLT
    21.0 100000004861 10027966 Morbid obesity LLT
    21.1 100000004865 10068900 Bariatric surgery LLT
    20.0 100000004865 10070978 Sleeve gastrectomy LLT
    20.0 100000004856 10019542 Hemorrhage gastric LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-018245-21 Sponsor Protocol Number: H-A-2009-069 Start Date*: 2010-06-22
    Sponsor Name:Rigshospitalet
    Full Title: Fibrinklæber ved bilateral knæalloplastik – et prospektivt randomiseret studie med fokus på: blodtab, smerte, ROM, hævelse og styrke
    Medical condition: Formålet med nærværende studie er at undersøge om – og i bekræftende fald omfanget heraf – fibrinklæber (Evicel) reducerer blødningen efter Total Knæ Alloplastik (kunstigt knæ)
    Disease: Version SOC Term Classification Code Term Level
    12.1 10044094 Total knee replacement LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
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    As of 31 January 2023, all EU/EEA initial clinical trial applications must be submitted through CTIS . Updated EudraCT trials information and information on PIP/Art 46 trials conducted exclusively in third countries continues to be submitted through EudraCT and published on this website.

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