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Clinical trials for Ambulatory surgery

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   44335   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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    92 result(s) found for: Ambulatory surgery. Displaying page 1 of 5.
    1  2  3  4  5  Next»
    EudraCT Number: 2019-003972-37 Sponsor Protocol Number: CLVSPR19 Start Date*: 2020-06-05
    Sponsor Name:Hospital Arnau de Vilanova - Lliria
    Full Title: Comparative study of cloroprocaine versus prilocaine intrathecal anestesia in major ambulatory surgery
    Medical condition: Inguinal hernia liable to ambulatory surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-001944-13 Sponsor Protocol Number: ZAA15CPP Start Date*: 2016-07-27
    Sponsor Name:Zaans Medisch Centrum
    Full Title: Chloroprocaine vs prilocaine for spinal anaesthesia in day-case surgery: a double-blind randomized trial
    Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive one of the two spinal anaesthetics
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: View results
    EudraCT Number: 2019-001079-35 Sponsor Protocol Number: PRPK Start Date*: 2019-08-29
    Sponsor Name:Cliniques universitaires Saint-Luc
    Full Title: A prospective randomized study in ambulatory patients undergoing upper limb bone surgery under single shot axillary plexus block.
    Medical condition: Do patients who are very painful when the axillary block wears off after bone surgery of the upper limb have a pre-existing central sensitization? Could this “rebound pain” be prevented by pre-inc...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2005-005949-19 Sponsor Protocol Number: CCOX189A2427 Start Date*: 2006-07-21
    Sponsor Name:Novartis Pharma Services AG
    Full Title: A multicenter, randomized, double-blind, placebo controlled, parallel group study to compare efficacy of a single dose of lumiracoxib 400 mg given preemptively versus post-operatively, in reducing ...
    Medical condition: Ambulatory arthroscopic knee surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Completed)
    Trial results: View results
    EudraCT Number: 2007-007019-10 Sponsor Protocol Number: AGO/2007/015 Start Date*: 2008-01-21
    Sponsor Name:University Hospital Ghent
    Full Title: Comparison of the therapeutic efficacy and side effects of tramadol per os (Tradonal Odis® orodispersible tablets) versus an optimised dosis of travenous tramadol for postoperative pain relief in a...
    Medical condition: Ambulatory surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2015-003987-35 Sponsor Protocol Number: Metamizole001 Start Date*: 2015-11-10
    Sponsor Name:JESSA Hospital
    Full Title: Metamizole versus NSAID at home after ambulatory surgery: a double-blind randomized controlled trial
    Medical condition: Pain after ambulatory surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2006-002901-30 Sponsor Protocol Number: AGO/2006/006 Start Date*: 2006-06-22
    Sponsor Name:University Hospital Ghent
    Full Title: Tramadol iv. : influence of dose and dose intervals on therapeutic accuracy and side effects when used for postoperative pain relief in ambulatory surgery
    Medical condition: ASA I and II
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2017-002559-27 Sponsor Protocol Number: 2017-03 Start Date*: 2018-03-29
    Sponsor Name:Zaans Medisch Centrum
    Full Title: ED50 and ED90 of intrathecal 1% chloroprocaine in day-case knee arthroscopy
    Medical condition: Patients scheduled for ambulatory knee arthroscopy surgery receive intrathecal chloroprocaine
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: NL (Completed)
    Trial results: (No results available)
    EudraCT Number: 2017-005074-19 Sponsor Protocol Number: BRIDION_ERASME Start Date*: 2018-04-06
    Sponsor Name:Erasme Hospital
    Full Title: Minimal optimal dose of Sugammadex during ambulatory surgery in dentistry
    Medical condition: women and men> 18 years of age Elective Surgery BMI <30, patients who gave consent to free and informed participation in writing to benefit from tooth extraction
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2018-001305-82 Sponsor Protocol Number: IC3627/18 Start Date*: 2019-05-16
    Sponsor Name:Laura Perelló Moreno
    Full Title: Study on the advantages of local post-operative infiltration in forefoot surgery.
    Medical condition: management of postoperative pain in ambulatory foot surgery that allows the realization of immediate rehabilitation and better functional results and personal satisfaction
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2015-002399-25 Sponsor Protocol Number: Sevo-Des-2015-01 Start Date*: 2015-11-04
    Sponsor Name:Servicio de Anestesia Infantil. Hospital Universitario La Paz
    Full Title: CLINICAL TRIAL TO COMPARE THE INCIDENCE AND CHARACTERISTICS OF POSTOPERATIVE AGITATION IN PEDIATRIC PATIENTS AFTER ANESTHESIA WITH SEVOFLURANE OR DESFLURANE IN AMBULATORY SURGERY.
    Medical condition: AGITATION AFTER POSTOPERATIVE ANESTHESIA IN PEDIATRIC PATIENTS
    Disease:
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2006-002890-31 Sponsor Protocol Number: Pregab1 Start Date*: 2006-08-25
    Sponsor Name:Dept. of Anaesthesia, Medical University of Vienna
    Full Title: Does Pregabalin reduce preoperative anxiety: a placebo controlled study
    Medical condition: Patients should receive Pregabalin or placebo as premedication one hour before ambulatory elective surgery. After this they have to assess their anxiety and pain with Visual Analog Scale (VAS) for ...
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: AT (Completed)
    Trial results: View results
    EudraCT Number: 2014-005026-35 Sponsor Protocol Number: 35RC14_9853_DEXA-OP Start Date*: Information not available in EudraCT
    Sponsor Name:Centre Hospitalier Universitaire de Rennes
    Full Title: Study DEXA-OP. Can the dexaméthasone replace the kétoprofène in the strategy of per-operating multimodal analgesia in pediatric ambulatory surgery? A double-blind randomized comparative study.
    Medical condition: Per-operating analgesia, pediatric ambulatory surgery
    Disease: Version SOC Term Classification Code Term Level
    18.0 100000004852 10002321 Anesthesia LLT
    18.0 10042613 - Surgical and medical procedures 10042609 Surgery PT
    Population Age: Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2011-001340-29 Sponsor Protocol Number: IIBSP-LEV-2011-21 Start Date*: 2011-09-16
    Sponsor Name:Institut de Recerca del Hospital de la Santa Creu i Sant Pau
    Full Title: Effectiveness of Added blocking of radial and median nerves with levobupivacaine in the control of postoperative pain in the rhizarthrosis ambulatory surgery
    Medical condition: Rhizarthrosis
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Completed)
    Trial results: View results
    EudraCT Number: 2013-000905-22 Sponsor Protocol Number: 5505 Start Date*: 2013-07-09
    Sponsor Name:Hôpitaux Universitaires de Strasbourg
    Full Title: à compléter
    Medical condition: akathisia
    Disease: Version SOC Term Classification Code Term Level
    18.0 10029205 - Nervous system disorders 10001540 Akathisia PT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-001789-42 Sponsor Protocol Number: IC01/04/DKP Start Date*: 2004-12-07
    Sponsor Name:Laboratorios Menarini, S.A.
    Full Title: A MULTICENTRE CLINICAL TRIAL EVALUATING THE ANALGESIC EFFICACY AND SAFETY OF DEXKETOPROFEN TROMETAMOL (50 mg i.v. FOLLOWED BY AN ORAL DOSAGE OF 25 mg t.i.d.) VERSUS METAMIZOL (2 g i.v. and 575 mg t...
    Medical condition: Patients who underwent ambulatory surgery consisting in unilateral inguinal mesh hernioplasty
    Disease: Version SOC Term Classification Code Term Level
    7.0 10022025 LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Completed)
    Trial results: View results
    EudraCT Number: 2019-002779-32 Sponsor Protocol Number: PREEMTIVE Start Date*: 2019-12-26
    Sponsor Name:BERTA CASTELLANO PAULIS
    Full Title: “Pre-emptive analgesia with Ibuprofen in outpatient laparoscopic cholecystectomy. Recovery Quality ”
    Medical condition: AMBULATORY LAPAROSCOPIC COLECISTECTOMY
    Disease:
    Population Age: Adults Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2013-000384-87 Sponsor Protocol Number: AGO/2013/001 Start Date*: 2013-03-05
    Sponsor Name:Ghent University Hospital
    Full Title: Intraperitoneal atomization of levobupivacaine during gynecological laparoscopic procedures : Impact on pain, opioid use and length of recovery room stay (IPLA).
    Medical condition: Patients who are planned for gynecological laparoscopic interventions on an ambulatory basis.
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004865 10002182 Analgesia LLT
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2014-005469-58 Sponsor Protocol Number: AGO/2014/007 Start Date*: 2015-01-14
    Sponsor Name:Ghent University Hospital
    Full Title: Determination of the minimum local anesthetic dose (MLAD) of spinal chloroprocaine for inguinal herniorrhaphy in ambulatory surgery.
    Medical condition: Inguinal herniorrhaphy.
    Disease: Version SOC Term Classification Code Term Level
    17.1 10042613 - Surgical and medical procedures 10022020 Inguinal hernia repair PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2019-002801-23 Sponsor Protocol Number: Metamizole002 Start Date*: 2019-10-08
    Sponsor Name:Jessa Hospital
    Full Title: Evaluation of the added value of Metamizole to standard post-operative treatment after ambulant surgery: a double-blind, randomized controlled trial
    Medical condition: Optimalization of post-operative treatment after ambulant surgery
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (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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