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Clinical trials for Cesarean section

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    The EU Clinical Trials Register currently displays   44341   clinical trials with a EudraCT protocol, of which   7370   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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    49 result(s) found for: Cesarean section. Displaying page 1 of 3.
    1  2  3  Next»
    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: 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: 2007-005269-36 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: 2014-000507-27 Sponsor Protocol Number: CarbetocinHeart2014 Start Date*: 2014-09-05
    Sponsor Name:Oslo University Hospital, Division of Emergencies and Critical Care
    Full Title: The Clinical Carbetocin Myocardium Trial
    Medical condition: Pregnancy
    Disease: Version SOC Term Classification Code Term Level
    17.0 10036585 - Pregnancy, puerperium and perinatal conditions 10036585 Pregnancy, puerperium and perinatal conditions SOC
    17.0 100000004865 10048862 Cesarean section LLT
    Population Age: Adults Gender: Female
    Trial protocol: NO (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)
    EudraCT Number: 2012-003188-23 Sponsor Protocol Number: 01-07-2012 Start Date*: 2012-09-28
    Sponsor Name:Merja Kokki
    Full Title:
    Medical condition:
    Disease: Version SOC Term Classification Code Term Level
    18.0 100000004863 10051798 Postoperative constipation LLT
    18.0 100000004856 10071128 Opioid induced constipation LLT
    18.0 100000004863 10054711 Postoperative pain LLT
    18.0 100000004865 10048862 Cesarean section LLT
    Population Age: Adults Gender: Female
    Trial protocol: FI (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: 2006-001506-81 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: 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: 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: 2013-004224-10 Sponsor Protocol Number: N/A Start Date*: 2013-12-06
    Sponsor Name:Region Skåne
    Full Title: Prospective randomized trial comparing the effects of oxytocin and carbetocin on circulation and vascular tone at cesarean section
    Medical condition: Cesarean section of pregnant women
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: SE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2012-001349-41 Sponsor Protocol Number: MD2012/1 Start Date*: 2012-05-15
    Sponsor Name:AZ Groeninge
    Full Title: Influence of dexamethasone on postoperative analgesia after combined spinal epidural for cesarean delivery.
    Medical condition: Postoperative pain
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    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: 2008-006235-12 Sponsor Protocol Number: OST10/08 Start Date*: 2009-06-30
    Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI
    Full Title: INTRATHECAL LEVOBUPIVACAINE USE IN CESAREAN SECTION : DETERMINATION OF �MINIMUM LOCAL ANESTHETIC DOSE (MLAD)�
    Medical condition: The aim of this study was to determine the Minimum Local Anesthetic Dose (MLAD) of subarachnoidal Levobupivacaine in cesarean section combined with opioid analgesics which are currently used for ce...
    Disease: Version SOC Term Classification Code Term Level
    12.0 10006921 Caesarean delivery (infant record) LLT
    Population Age: Adults Gender: Female
    Trial protocol: IT (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: 2005-006096-12 Sponsor Protocol Number: 87179098 Start Date*: 2006-07-06
    Sponsor Name:Karolinska University Hospital, Huddinge
    Full Title: Can peroperative subcutaneous, injection of bupivacaine with adrenaline decrease the postoperative need or opiates after cesarean section?
    Medical condition: Postoperative pain after cesarean section.
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: SE (Ongoing)
    Trial results: (No results available)
    EudraCT Number: 2017-004797-33 Sponsor Protocol Number: Obstetrics1.0 Start Date*: 2018-06-13
    Sponsor Name:CHU Tivoli
    Full Title: The efficacy of continuous ropivacaine wound infusion after cesarean delivery in pain management.
    Medical condition: Poor postoperative pain control leads to decreased satisfaction with care, prolonged recovery time and increased use of health care resources. Despite their efficacy, opioids are associated with na...
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Completed)
    Trial results: (No results available)
    EudraCT Number: 2015-001126-41 Sponsor Protocol Number: MVDV/MDS-12/2014 Start Date*: 2015-07-10
    Sponsor Name:University Hospitals Leuven
    Full Title: The effect of transversus abdominis plane block on postoperative analgesia after combined spinal epidural anesthesia for Cesarean delivery.
    Medical condition: providing adequate analgesia after cesarean delivery.
    Disease:
    Population Age: Adults Gender: Female
    Trial protocol: BE (Prematurely Ended)
    Trial results: View results
    EudraCT Number: 2008-006328-75 Sponsor Protocol Number: P071212 Start Date*: 2009-05-11
    Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP)
    Full Title: NOCETER essai multicentrique randomisé en double aveugle contre placebo. Réduction du taux de CEsariennes chez les patientes dépassant le TERme: Impact d'une maturation cervicale ambulatoire par do...
    Medical condition: Chez les femmes qui ont dépasser le terme d'accouchement (41 SA+0)
    Disease: Version SOC Term Classification Code Term Level
    8.1 10036656 Dépassement du terme d'accouchement (41SA+0) PT
    Population Age: Adults Gender: Female
    Trial protocol: FR (Ongoing)
    Trial results: (No results available)
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