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Clinical trials for Hysterectomy

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
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    • 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   44363   clinical trials with a EudraCT protocol, of which   7387   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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    3,306 result(s) found for: Hysterectomy. Displaying page 1 of 166.
    1  2  3  4  5  6  7  8  9  Next» Last»»
    EudraCT Number: 2009-012931-14 Sponsor Protocol Number: 20090518 Start Date*: 2010-06-10
    Sponsor Name:Landstinget Gävleborg
    Full Title: Smärtlindring efter Abdominell Hysterektomi - Är Blockad av Plexus Hypogastricus Superior en Effektiv Metod?
    Medical condition: Smärtlindring i samband med abdominell hysterektomi på benign indikation. Vi avser att studera om en peroperativt given nervblockad riktad mot plexus hypogastricus superior kan minska smärta och fö...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021152 Hysterectomy (ovaries conserved) LLT
    9.1 10000075 Abdominal hysterectomy LLT
    9.1 10021151 Hysterectomy LLT
    9.1 10042429 Subtotal hysterectomy LLT
    9.1 10042590 Supracervical hysterectomy LLT
    9.1 10044080 Total abdominal hysterectomy LLT
    9.1 10059806 Ovariohysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2012-005407-40 Sponsor Protocol Number: 2011-425 Start Date*: 2013-02-07
    Sponsor Name:Thomas Bergholt
    Full Title: Peroperative Tranexamic acid as prophylaxis of bleeding related to benign hysterectomy - a randomized, placebo-controlled trial
    Medical condition: Bleeding related to benign hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    14.1 100000004865 10066252 Total vaginal hysterectomy LLT
    14.1 100000004865 10046913 Vaginal hysterectomy LLT
    14.1 100000004865 10021152 Hysterectomy (ovaries conserved) LLT
    14.1 100000004865 10057318 Total hysterectomy LLT
    14.1 100000004865 10059806 Ovariohysterectomy LLT
    14.1 100000004865 10000075 Abdominal hysterectomy LLT
    14.1 100000004865 10027801 Modified vaginal hysterectomy LLT
    14.1 100000004865 10023692 Laparoscopically assisted hysterectomy LLT
    14.1 100000004865 10044080 Total abdominal hysterectomy LLT
    14.1 100000004865 10042429 Subtotal hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2008-005549-46 Sponsor Protocol Number: TS-005-DK Start Date*: 2009-01-21
    Sponsor Name:Hvidovre Hospital
    Full Title: A randomised, controlled prospective open parallel groups clinical trial for the evaluation of efficacy and safety of TachoSil® in women undergoing hysterectomy. A pilot study
    Medical condition: It is the intention with this clinical trial to evaluate wheter TachoSil may reduce the formation of postoperative haematomas on the vaginal cuff following hysterectomi. The presence of a postopera...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10044080 Total abdominal hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-001719-39 Sponsor Protocol Number: INN-CB-002 Start Date*: 2008-07-23
    Sponsor Name:Innocoll Technologies
    Full Title: A Phase II, Single Dose, Blinded, Prospective Study to Investigate the Efficacy and Safety of the CollaRx® Bupivacaine Implant in Women following Abdominal Hysterectomy or other Nonlaparoscopic Ben...
    Medical condition: To investigate the efficacy and safety of the CollaRx Bupivacaine Implant in women following abdominal hysterectomy or other nonlaparoscopic benign gynecological procedure
    Disease: Version SOC Term Classification Code Term Level
    9.1 10044080 Total abdominal hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2008-001125-34 Sponsor Protocol Number: 012008S Start Date*: 2008-05-08
    Sponsor Name:Arvi Yli-Hankala
    Full Title: Leikkauksen jälkeisen kivun voimakkuus propofoli- tai sevofluraanianestesian jälkeen.
    Medical condition: Potilaat tulevat tähystyksessä tehtävään kohdunpoistoleikkaukseen.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021151 Hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2021-003467-10 Sponsor Protocol Number: Naistenklinikka Start Date*: 2022-02-16
    Sponsor Name:HUS Naistenklinikka
    Full Title: Infections after hysterectomy - a placebo-controlled study comparing the profylactic use of azithromycin and cefuroxime with single cefuroxime
    Medical condition: Post-hysterectomy infections
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: FI (Trial now transitioned)
    Trial results: (No results available)
    EudraCT Number: 2006-003737-33 Sponsor Protocol Number: 2006-07 Start Date*: 2006-10-05
    Sponsor Name:Örebro University Hospital
    Full Title: Continuous Intraperitoneal Infusion of Local Anesthetics vs. Patient Controlled Intraperitoneal injection for Postoperative Pain relief following Abdominal Hysterectomy. A randomized, double-blind ...
    Medical condition: Postoperative pain after open abdominal hysterectomy
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2008-004867-21 Sponsor Protocol Number: 0663-097 Start Date*: 2008-11-18
    Sponsor Name:Merck & Co., Inc.
    Full Title: “Ensayo multicéntrico doble ciego controlado con placebo para estudiar la eficacia y la tolerabilidad de MK-0663/etoricoxib en el tratamiento del dolor después de histerectomía abdominal” A Double...
    Medical condition: Histerectomía Abdominal Abdominal Hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021151 Hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: ES (Completed) SE (Completed) EE (Completed) HU (Completed) IE (Completed) AT (Completed)
    Trial results: View results
    EudraCT Number: 2021-000874-28 Sponsor Protocol Number: 1 Start Date*: 2021-07-08
    Sponsor Name:Gyn.Dept, Aabenraa Hospital, Sygehus Sønderjylland
    Full Title: Effect of 24 mg dexamethasone preoperatively on surgical stress, pain and recovery in robotic-assisted laparoscopic hysterectomy
    Medical condition: robotic- assisted hysterectomy
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2008-003946-28 Sponsor Protocol Number: RC 29/08 Start Date*: 2009-02-04
    Sponsor Name:ISTITUTO PER L`INFANZIA BURLO GAROFOLO
    Full Title: Postoperative pain treatment following gynecologic surgery, using different doses of transdermal buprenorphine a double – blind, randomized study
    Medical condition: Patients elected for laparotomic hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    9.1 10021151 Hysterectomy LLT
    Population Age: Adults Gender: Female
    Trial protocol: IT (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2006-004998-95 Sponsor Protocol Number: KF5503/35 Start Date*: 2007-08-08
    Sponsor Name:Grünenthal GmbH
    Full Title: A randomized, double-blind, parallel-arm, placebo- and comparator-controlled trial of the efficacy and safety of multiple doses of immediate-release (IR) CG5503 for postoperative pain following abd...
    Medical condition: Postoperative pain following abdominal hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    8.1 10000075 Abdominal hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: HU (Completed) SK (Completed) LV (Completed) SI (Completed)
    Trial results: View results
    EudraCT Number: 2006-006839-51 Sponsor Protocol Number: AM-KSM-II/4/07 Start Date*: 2007-10-04
    Sponsor Name:Dr. Franz Köhler Chemie GmbH
    Full Title: Physostigmine induced reduction of analgetic treatment (PIRAT trial): Randomisiert kontrollierte Doppelblind-Studie zur analgetischen Wirkung einer postoperativen systemischen Applikation von Physo...
    Medical condition: female patients in need of getting an abdominal hysterectomy due to an illness
    Disease: Version SOC Term Classification Code Term Level
    9.1 10000075 Abdominal hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DE (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2008-003168-20 Sponsor Protocol Number: 08031RM-T Start Date*: 2008-08-12
    Sponsor Name:BELFAST HEALTH & SOCIAL CARE TRUST - BELFAST CITY HOSPITAL
    Full Title: Comparison of the effect of transversus abdominis plane block or conventional analgesia on pain scores, patient satisfaction and incidence of chronic pelvic pain after total abdominal hysterectomy.
    Medical condition: Transversus abdominis plane block for postoperative pain relief in patients undergoing total abdominal hysterectomy.
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2021-004562-35 Sponsor Protocol Number: Ketolorac_001 Start Date*: 2021-11-25
    Sponsor Name:Jessa ziekenhuis vzw
    Full Title: Low dose versus normal dose ketorolac for postoperative pain after prostatectomy and hysterectomy: a Double-blind Randomized Controlled Non-inferiority Trial
    Medical condition: Prostatectomy Hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    20.0 10042613 - Surgical and medical procedures 10061916 Prostatectomy PT
    20.0 10042613 - Surgical and medical procedures 10021151 Hysterectomy PT
    Population Age: Adults Gender: Male, Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2012-003787-51 Sponsor Protocol Number: NMBDK2012 Start Date*: 2012-10-22
    Sponsor Name:Mona Ring Gätke
    Full Title: Recovery after laparoscopic hysterectomy with deep neuromuscular blockade and low intraabdominal pressure
    Medical condition: The pain study: To evaluate the importance of deep neuromuscular blockade (NMB) and low intraabdominal pressure in laparoscopic hysterectomy considering postoperative pain, nausea, consumption of ...
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2018-004351-20 Sponsor Protocol Number: 01122018v2 Start Date*: 2019-02-01
    Sponsor Name:Aarhus University Hospital
    Full Title: Intraoperative methadone in same-day hysterectomy: a prospective, double-blind, randomised controlled trial
    Medical condition: Same-day hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    21.1 100000004865 10023692 Laparoscopically assisted hysterectomy LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2010-024538-51 Sponsor Protocol Number: ssgt05 Start Date*: 2012-03-02
    Sponsor Name:Silvia Gil Trujillo
    Full Title: Study of the effects of pregabalin in postoperative pain control in general total intravenous anesthesia, general inhalation anesthesia and combined anesthesia after abdominal hysterectomy.
    Medical condition: The presence of acute postoperative pain remains a major cause of preoperative morbidity.The objective is to evaluate the analgesic efficacy of pregabalin in the postoperatory of abdominal hysterec...
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: ES (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-005271-42 Sponsor Protocol Number: SM1-04 Start Date*: 2005-04-13
    Sponsor Name:Dept. of Anaestesiology, University hospital in Glostrup
    Full Title: Effect of paracetamol versus paracetamol combined with pregabalin versus paracetamol combined with pregabalin and dexamethason on pain and opioid requirements in patients scheduled for abdominal hy...
    Medical condition: Women scheduled for abdominal hysterectomy needs postoperative pain treatment, i.e. morphine. Morphine has side-effects: nausea, vomiting, sedation and dizziness. These side-effects are of course u...
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (Completed)
    Trial results: (No results available)
    EudraCT Number: 2004-005138-38 Sponsor Protocol Number: 2602-415 Start Date*: 2005-02-07
    Sponsor Name:Hvidovre Hospital
    Full Title: Antibiotikaprofylakse ved vaginalplastik
    Medical condition: Uterine prolapse grade I-II, cystocele and/or rectocele and/or enterocele grade I - IV and/or defects of the perineal body where there is medical indication for vaginal repair, but no indication fo...
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (Prematurely Ended)
    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)
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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
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