- Trials with a EudraCT protocol (61)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18)
61 result(s) found for: Obstetrics.
Displaying page 1 of 4.
EudraCT Number: 2016-000410-30 | Sponsor Protocol Number: EstrogenPOP2 | Start Date*: 2016-12-01 |
Sponsor Name:Medical University of Vienna, Department of Obstetrics and Gynecology | ||
Full Title: PREOPERATIVE LOCALLY APPLIED OESTROGEN IN POSTMENOPAUSAL WOMEN WITH PELVIC ORGAN PROLAPSE: CHANGES IN SUBJECTIVE AND OBJECTIVE OUTCOME: A PROSPECTIVE RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED ST... | ||
Medical condition: Pelvic organ prolapse | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001191-30 | Sponsor Protocol Number: IISR-2015-101127 | Start Date*: 2017-04-25 | |||||||||||
Sponsor Name:Department of Obstetrics & Gynecology, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
Full Title: Use of TachoSil® for the prevention of postoperative complications after groin dissection in vulva cancer patients | |||||||||||||
Medical condition: Vulva cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020824-23 | Sponsor Protocol Number: P-piller101 | Start Date*: 2010-09-01 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: P-piller och ekonomiskt beteende | ||
Medical condition: Healthy volontary young women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005770-57 | Sponsor Protocol Number: version121219 | Start Date*: 2013-03-25 |
Sponsor Name:department of OBstetrics, Sahlgrenska university hospital | ||
Full Title: Clinical effect of Atenativ treatment on uterine blood flow and the amount of Atenativ needed to maintain a normal antithrombin level during two weeks in early and severe preeclampsia | ||
Medical condition: Early and severe preeclampsia with low antithrombin activity. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000494-22 | Sponsor Protocol Number: 2004/120 | Start Date*: 2005-07-12 |
Sponsor Name:Department of Obstetrics and Gynecolog, Randers Centralsygehusy | ||
Full Title: Ny behandling af bartholins cyste/abscess med sølvnitrat | ||
Medical condition: Bartholins cyste/abscess | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-004984-23 | Sponsor Protocol Number: 191/2006 | Start Date*: 2008-05-08 |
Sponsor Name:Department of Obstetrics and Gynecology, Oulu University Hospital | ||
Full Title: Ehkäisylaastarin, ehkäisytabletin ja ehkäisyrenkaan vaikutukset hormonaalisiin, tulehduksellisiin ja aineenvaihdunnallisiin parametreihin hedelmällisessä iässä olevilla terveillä naisilla. | ||
Medical condition: Perusterveitä hedelmällisessä iässä olevia naisia. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001371-37 | Sponsor Protocol Number: GDM-TREAT | Start Date*: 2012-07-10 | ||||||||||||||||
Sponsor Name:Dr. med. Tina Vilsbøll | ||||||||||||||||||
Full Title: The impact of liraglutide on glucose tolerance and the risk of type 2 diabetes in women with previous gestational diabetes mellitus | ||||||||||||||||||
Medical condition: Gestational diabetes mellitus Non-alcoholic fatty liver disease | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000233-41 | Sponsor Protocol Number: OPTION | Start Date*: 2020-08-25 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: Labour induction in an outpatient setting - a multicenter randomized controlled trial. OPTION - OutPatienT InductiON | ||
Medical condition: Induction of labour | ||
Disease: | ||
Population Age: In utero, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000328-85 | Sponsor Protocol Number: FINNHT1 | Start Date*: 2017-05-18 | |||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Helsinki University Hospital, Obstetrics and Gynecology | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Randomized comparative trial between abrupt and tapered mode of discontinuation of longterm hormone therapy: Impact on endothelial function, recurrence of vasomotor symptoms and quality of life | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: We will assess the effects of hormone therapy termination on endothelial function using biophysical (flow-mediated dilation, peripheral artery tonometry) and biochemical markers. We will compare th... | |||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002271-36 | Sponsor Protocol Number: MEPIC | Start Date*: 2021-03-09 |
Sponsor Name:Danderyd Hospital | ||
Full Title: Mepivacaine for pain relief at insertion of intrauterine contraception (MEPIC) – a triple-blind randomized controlled trial. | ||
Medical condition: Insertion of intrauterine contraception | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000801-21 | Sponsor Protocol Number: 20130218 | Start Date*: 2014-08-26 |
Sponsor Name:Academic Medical Center | ||
Full Title: Stimulation of the ovaries in women with breast cancer undergoing fertility preservation: alternative versus standard stimulation protocols; the STIM-trial | ||
Medical condition: Ovarian stimulation in women with breast cancer prior to chemotherapy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020780-21 | Sponsor Protocol Number: W2010IM | Start Date*: 2011-03-28 |
Sponsor Name:Department of Obstetrics and Gynaecology, Karolinska Institutet, Stockholm | ||
Full Title: Paracervical block (PCB) during II-trimester abortion – a randomized controlled trial | ||
Medical condition: Pain during second trimester induced abortion | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006080-23 | Sponsor Protocol Number: DPMFM PC1036 | Start Date*: 2007-03-21 |
Sponsor Name:Institute of Obstetrics and Gynaecology Trust | ||
Full Title: Vitamin D status in pregnancy and the effects of vitamin D supplementation in ethnic minority groups | ||
Medical condition: Low vitamin D levels in pregnant women especially in ethnic minority groups | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000194-29 | Sponsor Protocol Number: OUHIVMproj-1-pco-hcg | Start Date*: 2006-04-11 |
Sponsor Name:Fertility Clinic, dept. of Obstetrics and gynecology, OUH. | ||
Full Title: In Vitro Maturation (IVM) as part of the treatment of infertility in women with polycystic ovaries (PCO). Is priming with hCG favourable? A prospective randomized study. | ||
Medical condition: Infertility in women with polycystic ovaries (PCO). | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-002015-22 | Sponsor Protocol Number: Strindfors2 | Start Date*: 2022-08-12 | |||||||||||
Sponsor Name:Dept. of Obstetrics and Gynecology, Sodersjukhuset | |||||||||||||
Full Title: A pilot study and randomized placebo-controlled trial on the effect and timing of oral Tranexamic acid (TA) administered prepartum on postpartum haemorrhage after vaginal delivery | |||||||||||||
Medical condition: Postpartum hemorrhage which is defined as bleeding during and after delivery that exceeds 500 ml. It is most commonly due to an atony of the uterus but may also have other causes such as tissue dam... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000782-22 | Sponsor Protocol Number: SAHA-Pilot-2016 | Start Date*: 2017-01-03 |
Sponsor Name:Medical University of Graz | ||
Full Title: A pilot study of peroral Vorinostat (Zolinza) in patients with refractory histone deacetylase-positive uterine sarcoma. | ||
Medical condition: Uterine sarcoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005247-14 | Sponsor Protocol Number: CHUB-Equidol | Start Date*: 2016-08-09 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: Effect of levobupivacaine infiltration versus placebo on perineal postpartum pain in episiotomy of primiparous, after instrumental delivery: randomized double blind clinical trial. | ||
Medical condition: Episiotomy (inclusion of primiparous patients giving birth by instrumental delivery -Suzor forceps, vacuum extraction, Thierry spatulas with episiotomy). | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-007669-21 | Sponsor Protocol Number: none | Start Date*: 2009-12-15 |
Sponsor Name:CHU of Liège | ||
Full Title: Effectiveness of prophylactic antibiotic intervention (fosfomycin trometamol) to prevent urinary tract infections due to urodynamic studies in women with urine incontinence or prolapsed: a randomi... | ||
Medical condition: The aim of the study is to assess the prophylactic use of antibiotics on urinary tract infection after urodynamic studies in women with incontinence or prolapse | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004050-29 | Sponsor Protocol Number: Vvax001-UMCG-02 | Start Date*: 2020-03-30 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: A phase II study to determine the efficacy and safety of Vvax001, a therapeutic Semliki Forest Virus based cancer vaccine, in patients with HPV-16 induced grade 3 cervical intraepithelial neoplasia. | ||
Medical condition: HPV-16 induced pre malignant cervical lesions | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000356-33 | Sponsor Protocol Number: oxy123 | Start Date*: 2013-03-27 | |||||||||||
Sponsor Name:Västra Götaland | |||||||||||||
Full Title: Delay in labour due to ineffective uterine contractions is still a major problem in modern obstetric care. It is one of the main reasons for the increased rate of operative deliveries, particularly... | |||||||||||||
Medical condition: Labor dystocia (LD) also referred to as prolonged labour is a commonly identified problem in modern delivery care with three described possible causes: inefficient uterine action, occiputposterior ... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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