- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
67 result(s) found for: Abortion.
Displaying page 1 of 4.
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: 2014-002974-35 | Sponsor Protocol Number: Tonab101 | Start Date*: 2014-10-07 |
Sponsor Name:Umeå University | ||
Full Title: Is home abortion mora acceptable for teenagers than abortion at the clinic? A randomized trial. | ||
Medical condition: Young women with unwanted pregnancies seeking abortion care | ||
Disease: | ||
Population Age: Adolescents, Under 18 | Gender: Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003675-35 | Sponsor Protocol Number: WV2018 | Start Date*: 2018-11-01 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Efficacy of Very Early Medical Abortion – a randomized controlled non-inferiority trial | ||
Medical condition: Unwanted pregnancy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) FI (Completed) AT (Ongoing) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002777-35 | Sponsor Protocol Number: 16I-Prg06 | Start Date*: 2017-01-18 | ||||||||||||||||||||||||||
Sponsor Name:IBSA INSTITUT BIOCHIMIQUE SA | ||||||||||||||||||||||||||||
Full Title: Prospective, double-blind, randomised, placebo controlled, phase III clinical study assessing the efficacy of natural progesterone 25 mg/bid administered subcutaneously in the maintenance of early ... | ||||||||||||||||||||||||||||
Medical condition: Threatened abortion | ||||||||||||||||||||||||||||
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Population Age: | Gender: Female | |||||||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004940-29 | Sponsor Protocol Number: SANNARU486 | Start Date*: 2005-01-13 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA O.I.R.M. - S. ANNA | |||||||||||||
Full Title: VOLUNTARY TERMINATION OF PREGNANCY WITH MIFEPRISTONE RU486 AND MISOPROSTOL | |||||||||||||
Medical condition: VOLUNTARY TERMINATION OF PREGNANCY LAW N.194/1978 | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001554-10 | Sponsor Protocol Number: NL57892 | Start Date*: 2016-06-21 | ||||||||||||||||
Sponsor Name:Radboudumc | ||||||||||||||||||
Full Title: Mifepristone and misoprostol versus misoprostol alone for uterine evacuation after early pregnancy failure: a pilot study | ||||||||||||||||||
Medical condition: Women aged above 18 years with early pregnancy failure, 6-14 weeks postmenstrual. | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-001447-43 | Sponsor Protocol Number: ALIFE2 | Start Date*: 2018-10-03 | |||||||||||
Sponsor Name:Academic Medical Center Amsterdam | |||||||||||||
Full Title: Anticoagulants for Living Fetuses in women with recurrent miscarriage and inherited thrombophilia; ALIFE2 study | |||||||||||||
Medical condition: recurrent miscarriage and inherited thrombophilia | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007661-20 | Sponsor Protocol Number: 1 | Start Date*: 2008-04-21 | |||||||||||
Sponsor Name:Lil Valentin, Region Skåne, Malmö University Hospital, Dpt Obstetrics and Gynecology [...] | |||||||||||||
Full Title: Which is the optimal treatment for miscarriage with a gestational sac in the uterus and which factors can predict if the treatment will be successful? | |||||||||||||
Medical condition: Miscarriage before 14 gestational weeks with a gestational sac in the uterus identified at ultrasound examiantion | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003760-36 | Sponsor Protocol Number: HUS277/03/2015 | Start Date*: 2016-01-20 |
Sponsor Name:HUS - Naistentautien ja synnytysten tulosyksikkö | ||
Full Title: Pain an medical abortion -Predicting factors of pain and optimal pain management among teenaged women compared to adult women | ||
Medical condition: Pain during Medical termination of pregnancy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005657-12 | Sponsor Protocol Number: HUS277/03/2015 | Start Date*: 2016-01-21 |
Sponsor Name:HUS - Naistentautien ja synnytysten tulosyksikkö | ||
Full Title: Pain an medical abortion -Predicting factors of pain and optimal pain management among teenaged women compared to adult women | ||
Medical condition: Pain during Medical termination of pregnancy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004749-18 | Sponsor Protocol Number: 201311LM | Start Date*: 2014-03-05 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: Home abortion up to 10 weeks of gestation | ||
Medical condition: Unwanted pregnancy and induced abortion | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-002856-28 | Sponsor Protocol Number: UF94602 | Start Date*: 2015-07-20 | |||||||||||
Sponsor Name:CHU de Montpellier | |||||||||||||
Full Title: Utilisation de l’Ultiva® associé à la Xylocaïne® dans les procédures de fœticide : essai randomisé de phase III | |||||||||||||
Medical condition: Interruptions Médicales de Grossesse (IMG) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000287-29 | Sponsor Protocol Number: 1 | Start Date*: 2018-03-23 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Immediate versus delayed insertion of intrauterine contraception at the time of medical abortion An open-label, randomized, multicenter study | ||
Medical condition: Post medical abortion contraception | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003143-11 | Sponsor Protocol Number: CHUBX201620 | Start Date*: 2016-10-27 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Effect of intra-venous ocytocine injection after fetal expulsion in management of third-stage of labor after second trimester medical pregnancy termination | |||||||||||||
Medical condition: second trimester medical pregnancy termination | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001505-26 | Sponsor Protocol Number: 2011-03-28WMA11 | Start Date*: 2011-11-02 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Repeated doses of misoprostol for medical treatment of missed abortion | ||
Medical condition: Intact miscarriage which has not been expelled from the body (missed abortion) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004083-35 | Sponsor Protocol Number: 2017-53 | Start Date*: 2018-03-28 |
Sponsor Name:Assistance Publique Hôpitaux de Marseille | ||
Full Title: A double-blind, randomized, multicenter study evaluating 200 mg versus 600 mg of Mifepristone on pain in voluntary abortion by drug prior to 7 SA. DoMy Study | ||
Medical condition: patient of 18 years or more, wishing an abortion with medication before 7 weeks of amenorrhea | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-000964-27 | Sponsor Protocol Number: WP2018 | Start Date*: 2018-05-09 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Medical termination of pregnancy from day 85 to day 153 of gestation: A randomized comparison between administration of the initial dose of misoprostol at home or in the clinic | ||
Medical condition: Unwanted pregnancy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-010277-21 | Sponsor Protocol Number: RG_09-015 | Start Date*: 2009-06-22 |
Sponsor Name:Calthorpe Clinic | ||
Full Title: A Randomised Controlled Trial on Efficacy of mifepristone followed by 6-8 hours versus 24 hours vaginal misoprostol in Early Pregnancy Abortions (< 63 days gestations) | ||
Medical condition: Medical termination of pregnancies before nine weeks of pregnancy | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2013-004294-27 | Sponsor Protocol Number: ISRCTN49711898 | Start Date*: 2014-06-23 |
Sponsor Name:Concept Foundation | ||
Full Title: Mifepristone and misoprostol for the termination of pregnancy at 64-140 days since LMP | ||
Medical condition: Termination of unwanted pregnancies of 64-140 days from last menses (verified by ultrasound) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003753-14 | Sponsor Protocol Number: 2016-35 | Start Date*: 2016-12-06 |
Sponsor Name:Assistance Publique Hôpitaux de Marseille | ||
Full Title: CERVICAL PREPARATION UNDER PARACERVICAL BLOCK FOR THE ABORTION OF FIRST TRIMESTER: RANDOMIZED TRIAL | ||
Medical condition: The women are 18 years old or more, wishing an abortion under local anesthesia, between 6 and 14 weeks the day of the abortion. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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