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Clinical trials for Hernia

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   44334   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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    85 result(s) found for: Hernia. Displaying page 1 of 5.
    1  2  3  4  5  Next»
    EudraCT Number: 2007-006707-21 Sponsor Protocol Number: arti2008 Start Date*: 2008-01-30
    Sponsor Name:Martina Bachmann
    Full Title: Päiväkirurginen spinaalipuudutus artikaiinilla verrattuna bupivakaiini-fentanyyliin
    Medical condition: Päiväkirurgiaan tuleva potilas, jolla on kirurgin arvioima tarve nivustyräleikkauksesta
    Disease: Version SOC Term Classification Code Term Level
    9.1 10019917 Hernia inguinal LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2009-011322-34 Sponsor Protocol Number: 0000 Start Date*: 2009-06-25
    Sponsor Name:Martina Bachmann
    Full Title: Päiväkirurginen spinaalipuudutus artikaiinilla verrattuna artikaiini-fentanyyliin
    Medical condition: Päiväkirurgiaan tuleva potilas, jolla on kirurgin arvioima tarve nivustyräleikkauksesta
    Disease: Version SOC Term Classification Code Term Level
    9.1 10019917 Hernia inguinal LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2006-004522-85 Sponsor Protocol Number: 4271055 Start Date*: 2006-05-30
    Sponsor Name:Hyks
    Full Title: Paravertebraalipuudutuksen merkitys päiväkirurgisten potilaiden spinaalipuudutuksessa tehdyn nivustyräleikkauksen jälkeiseen kipuun
    Medical condition: nivustyräleikkauksen jälkeinen postoperatiivinen kipu
    Disease: Version SOC Term Classification Code Term Level
    8.1 10022019 Inguinal hernia NOS LLT
    Population Age: Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-002878-35 Sponsor Protocol Number: GAS study Start Date*: 2008-07-15
    Sponsor Name:ISTITUTO GIANNINA GASLINI
    Full Title: The GAS study. A multi-site RCT comparing regional and general anaesthesia for effects on neurodevelopmental outcome and apnoea in infants
    Medical condition: Inguinal Hernia
    Disease: Version SOC Term Classification Code Term Level
    9.1 10022016 Inguinal hernia LLT
    Population Age: Preterm newborn infants, Newborns, Under 18 Gender: Male, Female
    Trial protocol: IT (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2009-011856-23 Sponsor Protocol Number: ERNPL Start Date*: 2009-09-16
    Sponsor Name:OSPEDALE POLICLINICO S. MATTEO
    Full Title: Evaluation of acute postsurgery pain management in patients who undergo inguen hernia surgery
    Medical condition: Acute post surgery pain in patients who undergo inguen hernia surgery
    Disease: Version SOC Term Classification Code Term Level
    9.1 10019917 LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2015-004916-39 Sponsor Protocol Number: 2015-806 Start Date*: 2016-01-19
    Sponsor Name:Digestive Disease Center, Bispebjerg Hospital
    Full Title: PreOperative Steroid in Abdominal Wall Reconstruction: A Double-blinded Randomized Clinical Trial
    Medical condition: Patients who undergo abdominal wall reconstruction for repair of a giant ventral hernia
    Disease: Version SOC Term Classification Code Term Level
    19.0 100000004856 10021620 Incisional hernias HLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2006-005494-21 Sponsor Protocol Number: MARIA Start Date*: 2006-11-23
    Sponsor Name:HYKS Marian sairaala
    Full Title: Hyperbaarisen artikaiini-glukoosiliuoksen ja pelkän artikaiinin vertailu spinaalipuudutuksessa nivustyräpotilailla
    Medical condition: nivustyrä
    Disease: Version SOC Term Classification Code Term Level
    8.1 10019909 Hernia LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2010-021851-23 Sponsor Protocol Number: ARHSG032010 Start Date*: 2011-04-19
    Sponsor Name:AZIENDA OSPEDALIERA S. GERARDO DI MONZA
    Full Title: analgesic effectiveness of ultrasound-guided ilioinguinal iliohypogastric and genitofemoral nerve block after inguinal herniorrhaphy
    Medical condition: Inguinal hernia elective surgery
    Disease: Version SOC Term Classification Code Term Level
    14.1 10017947 - Gastrointestinal disorders 10019917 Hernia inguinal LLT
    Population Age: Adults, Elderly Gender: Male
    Trial protocol: IT (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2010-019899-77 Sponsor Protocol Number: dx3 Start Date*: 2010-06-21
    Sponsor Name:Mette Astrup Madsen
    Full Title: Can preoperative Dexamethasone optimise surgical outcomes after laparoscopic inguinal hernia repair.
    Medical condition: Postoperative pain, nausea, vomiting, general well-being and convalescence after laparoscopic groin hernia repair.
    Disease: Version SOC Term Classification Code Term Level
    12.1 10019917 Hernia inguinal LLT
    12.1 10054711 Postoperative pain LLT
    12.1 10036901 Prophylaxis against postoperative nausea and vomiting LLT
    12.1 10016256 Fatigue LLT
    Population Age: Adults, Elderly Gender: Male
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2014-002802-19 Sponsor Protocol Number: NMBDKHernia2014 Start Date*: 2014-09-19
    Sponsor Name:Department of Anaesthesiology
    Full Title: Optimizing surgical conditions during laparoscopic umbilical, incisional –and linea alba herniotomy with deep neuromuscular blockade (The hernia study)
    Medical condition: The purpose of this study is to investigate surgical work space and surgical conditions in patients scheduled for laparoscopic umbilical, -linea alba and incisional herniotomy. The patients will ac...
    Disease: Version SOC Term Classification Code Term Level
    17.1 10018065 - General disorders and administration site conditions 10019909 Hernia PT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2005-002741-39 Sponsor Protocol Number: TIMELI001 Start Date*: 2005-12-07
    Sponsor Name:Prof. Giampiero CAMPANELLI
    Full Title: A prospective, controlled, randomized, patient and evaluator blinded study to evaluate pain and further disabling complications in patients undergoing Lichtenstein technique for primary inguinal he...
    Medical condition: Unilateral, uncomplicated primary inguinal hernia repair
    Disease: Version SOC Term Classification Code Term Level
    10022020
    Population Age: Adults, Elderly Gender: Male
    Trial protocol: GB (Completed) DE (Completed) ES (Completed) DK (Completed) IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2010-018403-29 Sponsor Protocol Number: SM1-plp-10 Start Date*: 2010-03-01
    Sponsor Name:Jørgen B. Dahl
    Full Title: Effekten af Transversus abdominis plane (TAP) block versus sårinfiltration versus placebo på patienter, der får foretaget åben operation for lyskebrok i dagkirurgisk regi
    Medical condition: Inguinal hernia repair
    Disease: Version SOC Term Classification Code Term Level
    12.1 10022020 Inguinal hernia repair LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2006-006295-37 Sponsor Protocol Number: 06/AN/04 Start Date*: 2007-04-05
    Sponsor Name:NHS Greater Glasgow & Clyde
    Full Title: A multi-site RCT comparing regional and general anaesthesia for effects on neurodevelopmental outcome and apnoea in infants.
    Medical condition: Inguinal hernia in neonates and infants
    Disease: Version SOC Term Classification Code Term Level
    8.1 10022016 Inguinal hernia PT
    Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 Gender: Male, Female
    Trial protocol: GB (Completed) NL (Ongoing)
    Trial results: (No results available)
    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: 2020-002945-41 Sponsor Protocol Number: 78464317 Start Date*: 2020-09-24
    Sponsor Name:Lone Nikolajsen
    Full Title: The use of intraoperative methadone in children undergoing open urological surgery
    Medical condition: Postoperative pain in children undergoing open urological surgery
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10031063 Orchiopexy LLT
    20.0 10010331 - Congenital, familial and genetic disorders 10011498 Cryptorchism PT
    20.0 100000004856 10022017 Inguinal hernias HLT
    20.0 10010331 - Congenital, familial and genetic disorders 10020488 Hydrocele PT
    Population Age: Infants and toddlers, Children, Under 18 Gender: Male
    Trial protocol: DK (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2009-013080-19 Sponsor Protocol Number: 27538 Start Date*: 2010-03-31
    Sponsor Name:AMC
    Full Title: Prokinetics to alter the position of the gastric acid pocket in Gastro Esophageal Reflux Disease
    Medical condition: gastro-esophageal reflux disease (GERD)
    Disease: Version SOC Term Classification Code Term Level
    9.1 10000479 Acid reflux (oesophageal) LLT
    9.1 10017884 Gastrooesophageal reflux LLT
    9.1 10017885 Gastrooesophageal reflux disease LLT
    9.1 10038262 Reflux esophagitis LLT
    9.1 10020024 Hiatal hernia LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: NL (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2018-001860-45 Sponsor Protocol Number: hospitalplato1 Start Date*: 2020-01-14
    Sponsor Name:Hospital Plató
    Full Title: Impact of topical antibiotic prophylaxis with Gentamicin on SSI rate on elective incisional hernia surgery: a randomised clinical trial.
    Medical condition: Surgical site infection on incisional hernia remains still high (8-14%). Its apperance is related to long and costfull treatments (daily cures, antibiotics and hospital readmission) and it is also ...
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2004-004670-88 Sponsor Protocol Number: 4975-2-007-2 Start Date*: 2005-05-23
    Sponsor Name:AlgoRx Pharmaceuticals, Inc.
    Full Title: A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Analgesic Efficacy, Safety and Tolerability of ALGRX 4975 in Subjects after Inguinal Hernia Repair
    Medical condition: Inguinal Hernia
    Disease: Version SOC Term Classification Code Term Level
    7.1 10022020 LLT
    Population Age: Adults, Elderly Gender: Male
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-004280-30 Sponsor Protocol Number: 20031209-2 Start Date*: 2004-12-30
    Sponsor Name:Landstinget Dalarna
    Full Title: Injestion of the steroid betamethasone during operation for inguinal hernia repair for purpose to optimize treatment of postoperative pain, reduction of postoperative discomfort like nausea and pos...
    Medical condition: Betamethasone will be studied for treatment of postoperative pain and discomfort after operations for inguinal hernia.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-002342-35 Sponsor Protocol Number: SKY0402-C-201 Start Date*: 2005-04-20
    Sponsor Name:SkyePharma, Inc.
    Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Dose-Escalating/De-Escalating Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of a Single Dose of Sustained-Release Encapsulated Bupiv...
    Medical condition: Pain following inguinal hernia repair
    Disease: Version SOC Term Classification Code Term Level
    6.0 10022020 LLT
    Population Age: Adults, Elderly Gender: Male
    Trial protocol: GB (Completed)
    Trial results: (No results available)
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    The status and protocol content of GB trials is no longer updated since 1 January 2021. For the UK, as of 31 January 2021, EU Law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland/NI. Legal notice
    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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