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Clinical trials for Hernias

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   44339   clinical trials with a EudraCT protocol, of which   7369   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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    17 result(s) found for: Hernias. Displaying page 1 of 1.
    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: 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: 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: 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: 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: 2008-004113-96 Sponsor Protocol Number: AGO/2008/008 Start Date*: 2008-09-17
    Sponsor Name:University Hospital Ghent
    Full Title: DRainage versus sEAlant in prospective, Monocentric, double blinded randomized trial to evaluate the effect of fibrin glue in surgical repair of incisional hernias (DREAM-trial)
    Medical condition: Open incisional hernia mesh repair
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: BE (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: 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: 2007-007013-37 Sponsor Protocol Number: O3-Hernia-EC07/90024 Start Date*: 2008-04-01
    Sponsor Name:Bernardino Clavo - Hospital Dr. Negrin
    Full Title: Ensayo Clínico aleatorizado del efecto de la Ozonoterapia en el tratamiento de la hernia de disco candidata a cirugía.
    Medical condition: Hernia de disco candidata a cirugia.
    Disease:
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: ES (Ongoing)
    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: 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: 2007-001298-27 Sponsor Protocol Number: 3200L-301-WW Start Date*: 2007-08-07
    Sponsor Name:Wyeth Research Division of Wyeth Pharmaceuticals Inc.
    Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of Intravenous Methylnaltrexone (MOA-728) for the Treatment of Postoperative Ileus After Ventral Hernia Repair
    Medical condition: Post operative ileus (POI). This study will examine the effect of IV MOA-728 versus placebo in shortening the time to return of bowel function in subjects receiving opioid analgesia administered v...
    Disease:
    Population Age: Gender: Male, Female
    Trial protocol: HU (Completed) NL (Completed) BE (Completed) IT (Completed) DE (Completed)
    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: 2020-003200-14 Sponsor Protocol Number: JR-141-GS31 Start Date*: 2022-05-16
    Sponsor Name:JCR Pharmaceuticals Co., Ltd.
    Full Title: A Phase III study of JR-141 in Mucopolysaccharidosis type II (Hunter Syndrome) patients.
    Medical condition: Mucopolysaccharidosis type II
    Disease: Version SOC Term Classification Code Term Level
    20.1 10010331 - Congenital, familial and genetic disorders 10056889 Mucopolysaccharidosis II PT
    Population Age: Children, Adolescents, Under 18, Adults Gender: Male, Female
    Trial protocol: DE (Trial now transitioned) FR (Trial now transitioned) PL (Trial now transitioned) IT (Trial now transitioned)
    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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