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Clinical trials for Abdominal hysterectomy

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    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).

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    147 result(s) found for: Abdominal hysterectomy. Displaying page 1 of 8.
    1  2  3  4  5  6  7  8  Next»
    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: 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: 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: 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: 2006-003737-33 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: 2010-018448-15 Sponsor Protocol Number: SJ-127 Start Date*: 2010-03-23
    Sponsor Name:Obstetrisk afd., Hvidovre Hospital
    Full Title: Effekten af præoperativ enkeltdosis methylprednisolon på det postoperative forløb efter abdominal hysterektomi: Et prospektivt, dobbeltblindet, placebo-kontrolleret studie.
    Medical condition: Postoperative pain after abdominal hysterectomy
    Disease: Version SOC Term Classification Code Term Level
    12.1 10000075 Abdominal hysterectomy LLT
    12.1 10054711 Postoperative pain LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DK (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: 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: 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: 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: 2011-003302-24 Sponsor Protocol Number: ESTEVE-SIGM-201 Start Date*: 2011-11-17
    Sponsor Name:Laboratorios Dr. Esteve S.A. (ESTEVE)
    Full Title: An exploratory, randomized, double blind, placebo controlled, parallel groups Phase II clinical trial to evaluate the efficacy and safety of E-52862 (400 mg) by oral route, as part of an analgesic ...
    Medical condition: post-operative pain following abdominal hysterectomy
    Disease:
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: ES (Completed)
    Trial results: View results
    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: 2016-004820-41 Sponsor Protocol Number: MK-7625A-035 Start Date*: 2017-08-23
    Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
    Full Title: A Phase 2, Randomized, Active Comparator-Controlled, Multicenter, Double-Blind Clinical Trial to Study the Safety and Efficacy of Ceftolozane/Tazobactam (MK-7625A) Plus Metronidazole Versus Meropen...
    Medical condition: Complicated intra-abdominal infection (cIAI)
    Disease: Version SOC Term Classification Code Term Level
    20.1 100000004862 10056570 Intra-abdominal infection LLT
    Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18 Gender: Male, Female
    Trial protocol: LT (Completed) ES (Completed) HU (Completed) Outside EU/EEA
    Trial results: View results
    EudraCT Number: 2011-005686-20 Sponsor Protocol Number: 004 Start Date*: 2012-08-20
    Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
    Full Title: A Phase II, Randomized, Active Comparator-Controlled Clinical Trial to Study the Safety, Tolerability, and Efficacy of MK-7655 + Imipenem/Cilastatin Versus Imipenem/Cilastatin Alone in Patients ...
    Medical condition: Patients with Complicated Intra-Abdominal Infection
    Disease: Version SOC Term Classification Code Term Level
    16.1 100000004862 10056570 Intra-abdominal infection LLT
    Population Age: Adults, Elderly Gender: Male, Female
    Trial protocol: DE (Completed) ES (Prematurely Ended) PT (Completed) GR (Completed) LT (Completed) LV (Completed) EE (Completed) BG (Completed) PL (Completed)
    Trial results: View results
    EudraCT Number: 2007-006121-26 Sponsor Protocol Number: BU-001-IM Start Date*: Information not available in EudraCT
    Sponsor Name:Nycomed Danmark ApS
    Full Title: An international, randomised, double blinded, multi-centre, active- and placebo-controlled dose response trial to evaluate the efficacy and safety of SABER-Bupivacaine for postoperative pain contro...
    Medical condition: Postoperative pain in patients undergoing primary, elective, open, abdominal hysterectomy.
    Disease: Version SOC Term Classification Code Term Level
    9.1 10054711 Postoperative pain LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: DE (Completed) GB (Prematurely Ended) HU (Completed) FR (Completed) SE (Completed) LV (Completed)
    Trial results: View results
    EudraCT Number: 2014-004081-21 Sponsor Protocol Number: FMLD-IOTRA-20_FIIIB Start Date*: 2015-01-02
    Sponsor Name:Laboratorios Farmalíder S.A.
    Full Title: A PHASE III, MULTICENTRE, INTERNATIONAL, RANDOMISED, DOUBLE-BLIND, DOUBLE-DUMMY, PARALLEL-GROUP, PLACEBO AND ACTIVE COMPARATORCONTROLLED CLINICAL TRIAL TO EVALUATE THE ANALGESIC EFFICACY AND SAFET...
    Medical condition: Evaluation of the analgesic efficacy in patients with moderate to severe pain after non-oncological abdominal surgery.
    Disease: Version SOC Term Classification Code Term Level
    17.1 10042613 - Surgical and medical procedures 10021151 Hysterectomy PT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: ES (Completed)
    Trial results: View results
    EudraCT Number: 2006-004049-41 Sponsor Protocol Number: TAP2 Start Date*: 2006-12-08
    Sponsor Name:Dept of Anaesthesia, University College Hospital, Galway
    Full Title: Determination of the efficacy of the Transversus Abdominis Plane (TAP) Block in the management of postoperative pain following Total Abdominal Hysterectomy (TAH).
    Medical condition: Post operative pain following Total Abdominal Hysterectomy.
    Disease: Version SOC Term Classification Code Term Level
    8.1 10054711 Postoperative pain LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: IE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2016-000818-29 Sponsor Protocol Number: MCP-103-403 Start Date*: 2016-08-08
    Sponsor Name:Ironwood Pharmaceuticals, Inc.
    Full Title: A Phase 4, Single-centre, Randomised, Double-blind, Placebo-controlled, Parallel-group, Fixed-dose Study of the Effect of Linaclotide on Abdominal Girth in Participants with Irritable Bowel Syndrom...
    Medical condition: Irritable Bowel Syndrome with Constipation
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004856 10066868 Constipation predominant irritable bowel syndrome LLT
    Population Age: Adults Gender: Male, Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: View results
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