- Trials with a EudraCT protocol (3,750)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,750 result(s) found for: Women's health.
Displaying page 1 of 188.
EudraCT Number: 2020-004780-71 | Sponsor Protocol Number: PROFERTIL | Start Date*: Information not available in EudraCT |
Sponsor Name:Karolinska University Hospital | ||
Full Title: A phase III Randomized Double-Blinded Placebo-Controlled Study of Use of GnRHa during Chemotherapy for Fertility Protection of Young Women and Teenagers with Cancer - ProFertil | ||
Medical condition: Breast Cancer Acute Leukemia Lymphomas (Hodgkin and non-Hodgkin) Sarcomas (Osteo, Soft tissue and Ewing) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-009014-40 | Sponsor Protocol Number: W2009M | Start Date*: 2009-07-20 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Pre-treatment with Mifepristone prior to Mirena insertion for optimizing bleeding pattern in pre-menopausal women | ||
Medical condition: The main objective of the present study is to study the effect of pre-treatment with Mifegyne in pre-menopausal women requesting Mirena for contraception in order to imrpove bleeding pattern during... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-000247-58 | Sponsor Protocol Number: PKZW-NZW201301 | Start Date*: 2013-09-30 |
Sponsor Name:KU Leuven Departement Ontwikkeling en Regeneratie | ||
Full Title: Pharmacokinetics of drugs used by pregnant women (paracetamol/macrolide antibiotics): in vivo pharmacokinetic study of pregnant versus non-pregnant women. | ||
Medical condition: 1) Pregnant women who, due to medical indication, need to take one of the experimental drugs (paracetamol, azithromycin or erythromycin) in the second or third trimester of there pregnancy 2) The s... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000599-25 | Sponsor Protocol Number: 3010 | Start Date*: 2008-05-09 |
Sponsor Name:TweeSteden Hospital | ||
Full Title: Iron and Folic acid v.s. Iron solely in the treatment of post partum anaemia, effects on haemoglobin and health status | ||
Medical condition: post partum anemia is generally treated by ferrous fumarate. It is unclear whether the addition of folic acid to ferrous fumarate in the treatment of anaemia could accelerate the increase of haemog... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002854-66 | Sponsor Protocol Number: | Start Date*: 2013-10-08 |
Sponsor Name:University Hospital Southampton NHS Foundation Trust | ||
Full Title: Southampton Pregnancy Intervention for the Next Generation - a randomised controlled trial of vitamin D and nurse support in improving the diet and body composition of young women and their children. | ||
Medical condition: We are not investigating a medical condition as such, but the effect of vitamin D on offspring body composition and bone mass, which are risk factors for later ill health. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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: 2017-000145-40 | Sponsor Protocol Number: versión2.febrero2017 | Start Date*: 2017-09-20 |
Sponsor Name:montserrat zamora brito | ||
Full Title: Use of acupuncture for the reduction of hospital admissions in the induction of labor due to chronologically prolonged gestation. ACUPUNT STUDY | ||
Medical condition: This Clinical Trial will evaluate the efficacy and safety of acupuncture to promote labor in pregnant women who need an induction at birth and thus be able to give answers to all these women who a... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005090-13 | Sponsor Protocol Number: "Painstudy"1 | Start Date*: 2017-04-18 |
Sponsor Name:Cancer Registry of Norway | ||
Full Title: Reducing painful colonoscopies in women participating in a colorectal cancer screening program: A randomized controlled trial | ||
Medical condition: Many women are experiencing pain under colonoscopy. The present study aims to reduce pain in women undergoing colonoscopy in a bowel cancer screening program in Norway. | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-003628-29 | Sponsor Protocol Number: REGC-15-035.R1 | Start Date*: 2015-12-01 |
Sponsor Name:University of Brighton | ||
Full Title: The introduction and use of Entonox as an alternative method of pain relief for intrauterine contraception device insertions. | ||
Medical condition: This study is to investigate the efficacy of 2 methods of pain relief during the procedure of an intrauterine contraceptive device insertion (coil). There is no medical condition or disease under i... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005666-37 | Sponsor Protocol Number: PrefoDIP | Start Date*: 2012-10-17 | |||||||||||
Sponsor Name:ZAMBON ITALIA | |||||||||||||
Full Title: Evaluation of the effect exerted by 5-methyltetrahydrofolate (5-MTHF) and folic acid in postmenopausal women | |||||||||||||
Medical condition: The study evaluates the effects of different forms of folates on cardiovascular risk factors in postmenopausal patients | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000440-22 | Sponsor Protocol Number: Version17032021 | Start Date*: 2021-03-25 |
Sponsor Name:Universiteit Antwerpen | ||
Full Title: Vaccination against COVID-19 in Pregnant and Lactating Women in Belgium | ||
Medical condition: Vaccine responses to COVID19 vaccines administered in pregnant and lactating women | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004188-38 | Sponsor Protocol Number: PHX401-14 | Start Date*: 2017-12-14 | |||||||||||
Sponsor Name:LABORATOIRE INNOTECH INTERNATIONAL | |||||||||||||
Full Title: Contraceptive Efficacy, Tolerance and Acceptability of A Benzalkonium Chloride Spermicide Cream In Women Aged Over 40 Years of Age - PHASE IV, INTERNATIONAL, OPEN-LABEL, MULTICENTRE, PROSPECTIVE STUDY | |||||||||||||
Medical condition: The current study is conducted in adult women over 40 years of age who need a contraceptive method and who accept to use a spermicide, according to the following inclusion/exclusion criteria and af... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2021-004536-28 | Sponsor Protocol Number: 1 | Start Date*: 2021-11-15 |
Sponsor Name:Uppsala University, Department of Women's and Children´s Health | ||
Full Title: Vaginal administration of selective estrogen receptor modulator (Tamoxifen) treatment to improve sexual function for women with breast cancer. A randomized, double-blinded, placebo controlled longi... | ||
Medical condition: Most troublesome vulvovaginal atrophy symptom | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001587-29 | Sponsor Protocol Number: 02/04/2020-001 | Start Date*: 2020-04-08 | |||||||||||
Sponsor Name:Barcelona Institute for Global Health (ISGlobal) | |||||||||||||
Full Title: Hydroxychloroquine efficacy in preventing SARS-CoV-2 infection and CoVid-19 disease severity during pregnancy | |||||||||||||
Medical condition: SARS-SoV-2 infection and CoVid-19 disease | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005891-28 | Sponsor Protocol Number: CORICA | Start Date*: 2008-10-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Perspective evaluation on the role practiced by three different contraceptive hormonal on l I risk cardiovascular in young women: impact on the sensibility' insulinica | |||||||||||||
Medical condition: GIOVANI DONNE TRA 18 E 35 ANNI | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000003-16 | Sponsor Protocol Number: UPBEAT-TIF | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Prevention of Gestational Diabetes in Obese Pregnant Women; a Proof of Principle Study Targeting Early Pregnancy Intervention to Women at Risk | |||||||||||||
Medical condition: Gestational diabetes mellitus | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005892-83 | Sponsor Protocol Number: WCH/2008/001 | Start Date*: 2009-01-14 |
Sponsor Name:Epsom and St Helier University Hospitals NHS Trust | ||
Full Title: Does metformin improve pregnancy outcomes [ incidence of LGA (≥90% birth weight centile) babies onset of maternal Gestational Diabetes, hypertension, PET, shoulder dystocia, admission to SCBU) in o... | ||
Medical condition: Obesity in pregnancy. Obesity in pregnancy has been identified by Confidential Enquiry into Maternal And Child Health (CEMACH) (2008-2011) as a major health risk to mother and baby. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-003343-74 | Sponsor Protocol Number: PDS234 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:Academic Medical Center | |||||||||||||
Full Title: A methodological investigation to test acute changes in female sexual desire in healthy volunteersand pre- and postmenopausal women diagnosed with hypoactive sexual desiredisordersusing explicit me... | |||||||||||||
Medical condition: hypoactive sexual desire disorder in women (HSDD) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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 |
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