- Trials with a EudraCT protocol (37)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
37 result(s) found for: Misoprostol.
Displaying page 1 of 2.
| EudraCT Number: 2015-003412-20 | Sponsor Protocol Number: DV-MV-MO | Start Date*: 2016-08-01 |
| Sponsor Name:Basque Health System | ||
| Full Title: Efficacy and safety of hourly titrated misoprostol versus vaginal dinoprostone and misoprostol for cervical ripening and labor induction: randomized clinical trial. | ||
| Medical condition: labor induction | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| 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: (No results available) | ||
| EudraCT Number: 2006-006371-20 | Sponsor Protocol Number: | Start Date*: 2007-11-30 | |||||||||||
| Sponsor Name:LUMC | |||||||||||||
| Full Title: Misoprostol in the management of retained placenta, a safe alternative for manual removal? A randomised controlled trial. | |||||||||||||
| Medical condition: To assess the effectiveness of misoprostol in the management of retained placenta. Will 800 micrograms of misoprostol orally reduce the need for manual removal under general anaesthesia and prove t... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| 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: 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: 2006-001201-28 | Sponsor Protocol Number: 2006-02-27UUS | Start Date*: Information not available in EudraCT |
| Sponsor Name:Department of Gynaecology, Helse Finnmark, Klinikk Hammerfest | ||
| Full Title: Self-administered vaginal misoprostol at home for cervical ripening prior to outpatient hysteroscopy: a randomised placebo-controlled trial. | ||
| Medical condition: Intrauterine pathology | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002061-29 | Sponsor Protocol Number: 08227 | Start Date*: 2016-03-21 | |||||||||||
| Sponsor Name:Consorci Sanitari de Terrassa | |||||||||||||
| Full Title: Prospective randomized clinical trial comparing the effect of vaginal misoprostol synchronously with supracervical ball, versus only vaginal misoprostol for induction of labor. | |||||||||||||
| Medical condition: Pegnant women with a term singleton pregnancy, cephalic presentation, reassuring fetal heart rate pattern, intact membranes and an unfavorable cervix (Bishop score less than 6), admitted to our ins... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-005097-35 | Sponsor Protocol Number: RG_16-076 | Start Date*: 2018-03-31 |
| Sponsor Name:University of Birmingham | ||
| Full Title: A randomised placebo-controlled trial of mifepristone and misoprostol versus misoprostol alone in the medical management of missed miscarriage | ||
| Medical condition: Missed miscarriage up to 13+6 weeks gestation. | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| 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: 2004-002051-13 | Sponsor Protocol Number: PANN3006 | Start Date*: 2005-08-17 |
| Sponsor Name:Imperial College, London | ||
| Full Title: A randomised double-blind placebo-controlled trial of oral misoprostol for cervical priming before outpatient hysteroscopy | ||
| Medical condition: Abnormal uterine bleeding (hysteroscopy to investigate and treatment of abnormal uterine bleeding) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002596-40 | Sponsor Protocol Number: A35148 | Start Date*: 2007-03-22 |
| Sponsor Name:World Health Organization | ||
| Full Title: Comparison of two doses and two routes of administration of misoprostol after pre-treatment with mifepristone for early pregnancy termination: a randomized, placebo-controlled, multicentre trial | ||
| Medical condition: Termination of early pregnancy | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002694-19 | Sponsor Protocol Number: 62449 | Start Date*: 2018-02-22 |
| Sponsor Name:Radboud University Medical Centre | ||
| Full Title: Mifepristone and misoprostol versus misoprostol alone for uterine evacuation after early pregnancy failure: a randomized double blind placebo-controlled comparison (M&M trial). | ||
| Medical condition: Early pregnancy failure | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-006897-60 | Sponsor Protocol Number: mis131206 | Start Date*: 2007-03-29 | |||||||||||
| Sponsor Name:Leids Universitair Medisch Centrum | |||||||||||||
| Full Title: Does Misoprostol facilitate the insertion of an Intra Uterine device (IUD), both copper-containing as well as levonorgestrel-releasing, with nulli- and multipara? | |||||||||||||
| Medical condition: Insertion of Intra Uterine Device (IUD) It is known that insertion of IUD sometimes fail or happen to be complicated (eg. by syncope, perforation of cervix or uterus or by creating a false passage... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003187-31 | Sponsor Protocol Number: GN09CA403 | Start Date*: 2015-03-19 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:NHS Greater Glasgow & Clyde | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Misoprostol for the Healing of Small Bowel Ulceration in Patients with Obscure Blood Loss while Taking Low-Dose Aspirin or Non-Steroidal Anti-inflammatory Drugs [MASTERS Trial] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Small bowel ulcers associated with iron deficiency anaemia or obscure blood loss in patients using aspirin or non-steroidal anti-inflammatory drugs | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (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: 2015-001972-23 | Sponsor Protocol Number: 2015-001972-23 | Start Date*: 2015-06-29 |
| Sponsor Name:Tampere University Hospital | ||
| Full Title: Randomized study to compare vaginal misoprostol to oral misoprostol in inducing labor | ||
| Medical condition: Pregnant women; induction of labor | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005160-23 | Sponsor Protocol Number: 2013 | Start Date*: 2013-05-02 |
| Sponsor Name:VU medical center | ||
| Full Title: Hismys study. Misoprostol for cervical priming prior to hysteroscopy in postmenopausal and nulliparous premenopausal women; a multi-centre randomised placebo controlled trial | ||
| Medical condition: Reduction of pain during hysteroscopy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-002965-20 | Sponsor Protocol Number: MISFOL2018 | Start Date*: 2019-05-14 | |||||||||||
| Sponsor Name:SOLEDAD CARREGUI, NATIVIDAD BANEGAS, SARA CRUZ | |||||||||||||
| Full Title: A randomized, open, 2 treatment arms clinical trial to evaluate the efficacy and safety of cervical ripening with Foley catheter vs cervical ripening with intravaginal synthetic analogue of prostag... | |||||||||||||
| Medical condition: Cervical ripening prior labor induction | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000026-30 | Sponsor Protocol Number: ABR35278 | Start Date*: 2013-05-08 | |||||||||||
| Sponsor Name:Academic medical centre | |||||||||||||
| Full Title: Induction of Labour with a Foley catheter or oral Misoprostol at Term | |||||||||||||
| Medical condition: Induction of labour at term | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (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 (Ongoing) | ||
| Trial results: (No results available) | ||
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