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Clinical trials for Caesarean section

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    The EU Clinical Trials Register currently displays   44338   clinical trials with a EudraCT protocol, of which   7368   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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    92 result(s) found for: Caesarean section. Displaying page 1 of 5.
    1  2  3  4  5  Next»
    EudraCT Number: 2012-002068-29 Sponsor Protocol Number: 1-09-09-2012 Start Date*: 2012-12-03
    Sponsor Name:Jan Stener Joergensen
    Full Title: Antibiotic Prophylaxis and Intervention for Postpartum Infections following Caesarean Section
    Medical condition: Sub-study 1: women delivering a child by caesarean section Sub-study 2: Women, who are hospitalized at the obstetrical ward for reoperation because of superficial or deep infection or haematoma...
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2006-005635-25 Sponsor Protocol Number: 1395 Start Date*: 2006-11-15
    Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI
    Full Title: Postoperative pain after cesarean section :efficacy of S-ketamine at antihyperalgesic doses.
    Medical condition: Postoperative pain after cesarean section
    Disease: Version SOC Term Classification Code Term Level
    6.1 10006924 PT
    Population Age: Adults Gender: Female
    Trial protocol: IT (Completed)
    Trial results: (No results available)
    EudraCT Number: 2007-002949-20 Sponsor Protocol Number: LWH0747 Start Date*: 2008-04-28
    Sponsor Name:Liverpool Women's NHS Foundation Trust
    Full Title: Randomised controlled trial comparing the effects of oxytocin 5 units IV bolus vs oxytocin 5 units IV infusion on cardiac output during caesarean section
    Medical condition: The drug is given routinely to women during caesarean section to help the womb contract after their baby has been delivered. This helps reduce the risk of bleeding after surgery. For this trial, ...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10006924 Caesarean section LLT
    Population Age: Adults Gender: Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2006-004799-11 Sponsor Protocol Number: 2006OB01 Start Date*: 2007-11-29
    Sponsor Name:Coombe Women's Hospital
    Full Title: A randomised trial of oxytocin bolus versus oxytocin bolus and infusion for the control of blood loss at elective caesarean section.
    Medical condition: Elective lower segment caesarean section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: IE (Completed)
    Trial results: View results
    EudraCT Number: 2007-005231-28 Sponsor Protocol Number: 31121976-1 Start Date*: 2008-10-01
    Sponsor Name:Med. Univ. Wien, Universitätsklinik für Anästhesie, allgemeine Intensivmedizin und Schmerzmedizin
    Full Title: Postoperative Analgesie and Antihyperalgesia of Tramadol and Acetaminophen peroral after Caesarean Section
    Medical condition: Pain after Cesarean Section in spinal anesthesia
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: AT (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2006-001506-81 Sponsor Protocol Number: 35/2006/U/Sper Start Date*: 2006-05-03
    Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI
    Full Title: SPINAL ANESTHESIA IN THE CAESAREAN CUT LEVOBUPIVACAINE VERSUS ROPIVACAINE VERSUS HYPERBARIC BUPIVACAINE
    Medical condition: Subaracnoidea anesthesia in the Caesarean Cut
    Disease: Version SOC Term Classification Code Term Level
    8.1 10006924 Caesarean section LLT
    Population Age: Adults Gender: Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2007-006275-36 Sponsor Protocol Number: 0708097 Start Date*: 2008-02-11
    Sponsor Name:CHU de Saint-Etienne
    Full Title: Levobupivacaine into post-caesarian analgesia: randomized monocentric study against placebo
    Medical condition: post-caesarean analgesia
    Disease: Version SOC Term Classification Code Term Level
    9.1 10006924 Caesarean section LLT
    9.1 10021415 Immediate postoperative analgesia LLT
    Population Age: Adults Gender: Female
    Trial protocol: FR (Completed)
    Trial results: (No results available)
    EudraCT Number: 2007-000392-42 Sponsor Protocol Number: anaes071 Start Date*: 2007-06-14
    Sponsor Name:Department of Anaesthesia, Rotunda Hospital
    Full Title: Transversus Abdominis Plane (TAP) Block with or without intrathecal morphine for analgesia following lower segment Caesarean Section
    Medical condition: This trial investigates four techniques for analgesia provision after Elective Lower Segment Caesarean Section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: IE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-001361-34 Sponsor Protocol Number: 2004OB04 Start Date*: 2005-04-26
    Sponsor Name:University of Dundee
    Full Title: A randomised controlled trial of oxytocin 5 IU versus oxytocin 5 IU and 30 IU infusion for the control of blood loss at elective caesarean section - pilot study.
    Medical condition: Elective lower segment caesarean section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2008-006080-36 Sponsor Protocol Number: PHT/2008/42 Start Date*: 2009-01-29
    Sponsor Name:Portsmouth Hospitals NHS Trust
    Full Title: Analgesic efficacy of ultrasound guided transversus abdominis plane block as part of a multimodal analgesic regime for post elective caesarean section pain – a comparative double-blinded placebo co...
    Medical condition: This study is aimed at improving pain relief for women undergoing a planned caesarean section. Current pain relieving regimes are not ideal and often lead to women experiencing considerable pain af...
    Disease: Version SOC Term Classification Code Term Level
    9.1 10036276 Postoperative analgesia LLT
    9.1 10024977 Lower segment Caesarean section LLT
    Population Age: Adults Gender: Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: (No results available)
    EudraCT Number: 2004-004278-10 Sponsor Protocol Number: 2004/R/AN/04 Start Date*: 2005-02-10
    Sponsor Name:Lothian Health Board- University Hospitals Division [...]
    1. Lothian Health Board- University Hospitals Division
    2. Lothian Health Board University Hospitals Division
    Full Title: Determination of the subarachnoid ED50 and ED95 of hyperbaric 0.5% bupivacaine when co-administered with diamorphine hydrochloride for caesarean section
    Medical condition: patients undergoing elective caesarean section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2020-005681-33 Sponsor Protocol Number: MVDVER102020 Start Date*: 2021-03-18
    Sponsor Name:University Hospitals Leuven
    Full Title: High versus low-dose dexamethasone for postoperative anagesia after caesarean section: a randomised, double-blind, two-center study.
    Medical condition: postoperative analgesia after Caesarean section
    Disease: Version SOC Term Classification Code Term Level
    21.1 10042613 - Surgical and medical procedures 10036276 Postoperative analgesia PT
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2016-000813-63 Sponsor Protocol Number: TACs Start Date*: 2016-04-06
    Sponsor Name:Universitair Ziekenhuis Brussel
    Full Title: Comparative doubleblind study with prilocaine 2 % and 2-chloroprocaine for elective caesarean section.
    Medical condition: Healthy pregnant women undergoing a elective caesarean section with an uncomplicated pregnancy of a singleton, "full-term", all between 18-40 y (ASAI-II) through combined spinal and epidural approach.
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: View results
    EudraCT Number: 2014-001705-40 Sponsor Protocol Number: ju2014 Start Date*: 2015-02-09
    Sponsor Name:Tampereen yliopistollinen sairaala
    Full Title: Laskimonsisäinen PCA (patient-controlled analgesia) -oksikodoni verrattuna suun kautta otettavaan oksikodoniin keisarileikkauksen jälkeisen kivun lievityksessä – satunnaistettu vertaileva tutkimus
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    17.1 10042613 - Surgical and medical procedures 10006924 Caesarean section PT
    Population Age: Adults Gender: Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2005-002812-94 Sponsor Protocol Number: LOXY v3 Start Date*: 2005-09-09
    Sponsor Name:North Bristol NHS Trust
    Full Title: Randomised trial of carbetocin versus oxytocin for the prevention of postpartum haemorrhage after caesarean section
    Medical condition: Postpartum haemorrhage after caesarean section
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: GB (Completed)
    Trial results: View results
    EudraCT Number: 2018-003960-29 Sponsor Protocol Number: 11102018 Start Date*: 2018-12-18
    Sponsor Name:Turku University Hospital
    Full Title: Improving cesarean section practices - focus on bleeding and infection complications
    Medical condition: Cesarean section complications (bleeding, infections, tromboembolic complications)
    Disease: Version SOC Term Classification Code Term Level
    20.0 100000004865 10048862 Cesarean section LLT
    Population Age: Adults Gender: Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
    EudraCT Number: 2007-005269-36 Sponsor Protocol Number: 92/2007/O/Sper Start Date*: 2007-09-18
    Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI
    Full Title: INTRATHECAL ROPIVACAINE USE IN CESAREAN SECTION : DETERMINATION OF “MINIMUM LOCAL ANESTHETIC DOSE (MLAD)”
    Medical condition: cesarean section
    Disease: Version SOC Term Classification Code Term Level
    6.1 10006924 PT
    Population Age: Adults Gender: Female
    Trial protocol: IT (Completed)
    Trial results: View results
    EudraCT Number: 2010-021783-15 Sponsor Protocol Number: Version 1.0 Start Date*: 2010-12-31
    Sponsor Name:Guys and St Thomas' NHS Foundation Trust
    Full Title: Ropivacaine 0.75% versus Levobupivacaine 0.5% for conversion of labour epidural to surgical anaesthesia for emergency Caesarean section. (RoLe Trial)
    Medical condition: Conversion of labour epidural to surgical anaesthesia for emergency Caesarean section
    Disease: Version SOC Term Classification Code Term Level
    12.1 10006924 Caesarean section LLT
    12.1 10054375 Epidural anesthesia LLT
    Population Age: Adults, Elderly Gender: Female
    Trial protocol: GB (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2017-003625-15 Sponsor Protocol Number: Cath_TQL_caesarean_version1 Start Date*: 2018-06-22
    Sponsor Name:Zealand university hospital, Roskilde
    Full Title: Ultrasound-guided Transmuscular Quadratus Lumborum catheters for elective caesarean section. A double blind, randomised, placebo controlled trial.
    Medical condition: Treatment of postoperative pain after elective caesarean section.
    Disease: Version SOC Term Classification Code Term Level
    20.1 100000004863 10054711 Postoperative pain LLT
    20.0 100000004865 10006832 C-section LLT
    Population Age: Adults Gender: Female
    Trial protocol: DK (Completed)
    Trial results: View results
    EudraCT Number: 2010-020888-20 Sponsor Protocol Number: 03052010 Start Date*: 2010-09-16
    Sponsor Name:Merja Kokki
    Full Title: LASKIMOON ANNETUN FENTANYYLIN TEHO, TURVALLISUUS JA PITOISUUDET PLASMASSA KEISARILEIKKAUKSEN YHTEYDESSÄ
    Medical condition: Tutkittavat ovat terveitä synnyttäjiä, joilla on täysiaikainen raskaus ja jotka tulevat suunniteltua sektiota varten sairaalaan
    Disease: Version SOC Term Classification Code Term Level
    12.1 10010273 Pregnancy, labour, delivery and postpartum conditions HLGT
    12.1 10048862 Cesarean section LLT
    Population Age: In utero, Newborns, Under 18, Adults Gender: Female
    Trial protocol: FI (Completed)
    Trial results: (No results available)
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