- Trials with a EudraCT protocol (331)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
331 result(s) found for: Endometrial.
Displaying page 8 of 17.
| EudraCT Number: 2012-003405-98 | Sponsor Protocol Number: dexFEMv2 | Start Date*: 2012-12-03 | |||||||||||
| Sponsor Name:ACCORD University of Edinburgh [...] | |||||||||||||
| Full Title: Developmental Clinical Studies - Reversing endometrial glucocorticoid deficiency in heavy menstrual bleeding | |||||||||||||
| Medical condition: Endometrial glucocorticoid deficiency in Heavy Menstrual Bleeding | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002662-12 | Sponsor Protocol Number: GINECO-EN203b | Start Date*: 2020-01-16 | ||||||||||||||||||||||||||
| Sponsor Name:ARCAGY-GINECO | ||||||||||||||||||||||||||||
| Full Title: A multicentric randomized phase II/III evaluating TSR-042 (anti-PD-1 mAb) in combination with Niraparib (parpi) versus Niraparib alone compared to chemotherapy in the treatment of metastatic or rec... | ||||||||||||||||||||||||||||
| Medical condition: metastatic or recurrent endometrial or ovarian carcinosarcoma | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-002689-68 | Sponsor Protocol Number: NL.23273.08 | Start Date*: 2009-03-10 | |||||||||||
| Sponsor Name:Isala Klinieken, location Sophia | |||||||||||||
| Full Title: Cryo-thawed embryo transfer: natural versus artificial cycle. A non inferiority trial. | |||||||||||||
| Medical condition: Subfertility in need of IVF and IVF-ICSI treatment. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017245-64 | Sponsor Protocol Number: OG09/9146 | Start Date*: 2010-09-07 |
| Sponsor Name:Leeds Teaching Hospitals NHS Trust | ||
| Full Title: The effect of metformin co-treatment in hormone-replacement frozen embryo replacement cycles in women with polycystic ovary syndrome. | ||
| Medical condition: Polycystic Ovary Syndrome | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004340-32 | Sponsor Protocol Number: 308961 | Start Date*: 2006-04-20 |
| Sponsor Name:Bayer Schering Pharma AG | ||
| Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group, Placebo-Controlled, 7 Cycle Duration (196 Days), Phase 3 Study of Oral Estradiol Valerate/Dienogest Tablets for the Treatment of Dysfunction... | ||
| Medical condition: Treatment of prolonged, excessive or frequent bleeding in women without organic pathology who desire oral contraception. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: GB (Completed) SE (Completed) DE (Completed) FI (Completed) HU (Completed) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-003645-16 | Sponsor Protocol Number: 2019_0012 | Start Date*: 2020-02-25 |
| Sponsor Name:Hopital Foch | ||
| Full Title: Benefit of the GnRH agonist before frozen embryo transfer in patients with endometriosis and / or adenomyosis: randomized prospective study | ||
| Medical condition: Frozen embryo transfer in patients with endometriosis and/or adenomyosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002536-32 | Sponsor Protocol Number: GREEN-EX | Start Date*: 2023-07-06 | |||||||||||||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||||||||||||
| Full Title: Indocyanine green to assess vascularity of ileal conduit anastomosis and regulate ureteral resection margins during pelvic exenteration for recurrent/persistent gynecological cancer. A pilot study | |||||||||||||||||||||||
| Medical condition: Patients with gynecological cancers undergoing pelvic exenteration | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2013-002109-73 | Sponsor Protocol Number: NiCCC2013 | Start Date*: 2013-11-14 | ||||||||||||||||
| Sponsor Name:Greater Glasgow Health Board | ||||||||||||||||||
| Full Title: A Randomised Phase II Study of Nintedanib (BIBF1120) Compared to Chemotherapy in Patients with Recurrent Clear Cell Carcinoma of the Ovary or Endometrium | ||||||||||||||||||
| Medical condition: Recurrent clear cell carcinoma of the ovary or endometrium | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: GB (Completed) FR (Completed) NL (Completed) DK (Prematurely Ended) FI (Prematurely Ended) NO (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-005474-11 | Sponsor Protocol Number: Pro.V.En | Start Date*: 2015-08-18 | |||||||||||
| Sponsor Name:USS Centro di Fisiopatologia della Riproduzione, A.O. Papa Giovanni XXIII | |||||||||||||
| Full Title: Pilot clinical study multicenter, prospective, randomized, open, non-profit to evaluate the efficacy of progesterone administered with different dose subcutaneously compared to progesterone adminis... | |||||||||||||
| Medical condition: Women undergoing assisted reproduction with autologous cryopreserved embryo transfer. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-003307-36 | Sponsor Protocol Number: LWH0606 | Start Date*: 2005-12-08 |
| Sponsor Name:University of Liverpool/Liverpool Women's Hospital | ||
| Full Title: A randomised controlled trial of prednisolone for women with recurrent miscarriage and high levels of uNK cells in the endometrium | ||
| Medical condition: Idopathic recurrent miscarriage | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2021-005005-28 | Sponsor Protocol Number: ADENOFERT | Start Date*: 2022-11-08 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA DI MODENA | |||||||||||||
| Full Title: Assisted reproductive technology (ART) and pregnancy outcomes in women with adenomyosis (internal endometriosis) according to stimulation protocol in relation to immunological and endometrial featu... | |||||||||||||
| Medical condition: Women with transvaginal ultrasound (TV-US)-based diagnosis of adenomyosis and women without adenomyosis but with similar baseline reproductive risks | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-002997-38 | Sponsor Protocol Number: BAY1002670/15787 | Start Date*: 2018-01-10 | |||||||||||||||||||||
| Sponsor Name:Bayer AG | |||||||||||||||||||||||
| Full Title: A randomized, parallel-group, double-blind and open-label, placebo-controlled, multicenter study to assess the efficacy and safety of vilaprisan in subjects with uterine fibroids | |||||||||||||||||||||||
| Medical condition: Leiomyoma | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||||||||||||
| Trial protocol: CZ (Completed) BG (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2016-003975-23 | Sponsor Protocol Number: IGX1-ENT-XS-16-01 | Start Date*: 2020-04-20 | |||||||||||
| Sponsor Name:Asherman Therapy S.L.U. | |||||||||||||
| Full Title: Efficacy and safety of autologous, mobilized, non-expanded CD133+ cells to treat Asherman´s Syndrome: A prospective, multi-center, phase I/II clinical trial. | |||||||||||||
| Medical condition: Asherman's syndrome also known as intrauterine synechiae | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000001-25 | Sponsor Protocol Number: OXO-001-201 | Start Date*: 2021-08-06 |
| Sponsor Name:Oxolife S.L. | ||
| Full Title: A phase II, randomised, double-blind, parallel-group, placebo-controlled trial to assess the ongoing pregnancy rate with OXO-001 (200 mg, 300 mg) or placebo at 10 weeks following fresh single blast... | ||
| Medical condition: Infertility treatment and fertility enhancer in women undergoing assisted reproductive techniques or natural reproduction | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: PL (Completed) ES (Ongoing) CZ (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-000172-38 | Sponsor Protocol Number: NP137-CT-02 | Start Date*: 2020-09-04 | |||||||||||||||||||||||||||||||
| Sponsor Name:NETRIS PHARMA | |||||||||||||||||||||||||||||||||
| Full Title: A randomised, multicentre, open label, Phase I/II study to evaluate the safety (Phase I - safety run in), clinical and biological activity (Phase II) of a humanized monoclonal antibody targeting Ne... | |||||||||||||||||||||||||||||||||
| Medical condition: Locally advanced/metastatic endometrial carcinoma or cervix carcinoma progressing/relapsing after at least one prior systemic chemotherapy. | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-000115-32 | Sponsor Protocol Number: EVE112-CT02-2015 | Start Date*: 2016-02-25 | |||||||||||
| Sponsor Name:Evestra GmbH | |||||||||||||
| Full Title: Characterization of ovulation inhibition of a new vaginal delivery system (EVE 112, Evestra/Germany) containing etonogestrel and ethinylestradiol – an open label, single centre, comparative, parall... | |||||||||||||
| Medical condition: Investigation of ovulation inhibition for indication of contraception. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2015-000206-18 | Sponsor Protocol Number: PM1183-B-005-14-QT | Start Date*: 2015-09-10 | |||||||||||
| Sponsor Name:PharmaMar S.A., Sociedad Unipersonal | |||||||||||||
| Full Title: Evaluation of the Effect of Lurbinectedin (PM01183) on Cardiac Repolarization (QTc Duration) in Patients with Selected Solid Tumors | |||||||||||||
| Medical condition: - small cell lung cancer (SCLC) - head and neck carcinoma (H&N) - neuroendocrine tumors (NETs) - biliary tract carcinoma - endometrial carcinoma - BRCA 1/2-associated metastatic breast carcinoma - ... | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-002540-26 | Sponsor Protocol Number: A/644/05 | Start Date*: 2006-02-16 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Evalutation of the effects of non pegylated liposomial doxorubicin MYOCET on the reduction of skin and cardiac toxicity in platinum resistant ovarian and endometrial cancer patients . A phase I... | |||||||||||||
| Medical condition: second line treatment in platinum resistant ovarian and endometrial cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-006069-34 | Sponsor Protocol Number: 1564 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Clinical efficacy and cell mobilization activity of pegfilgrastim in patients with gynaecological malignancies in therapy with topotecan. | |||||||||||||
| Medical condition: ovarian cancer, cervical cancer, endometrial cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-001789-13 | Sponsor Protocol Number: QUINA/2012 | Start Date*: 2012-11-16 |
| Sponsor Name:Instituto de Investigacion Sanitaria La e | ||
| Full Title: Double-blind, randomized, controlled contraceptives, parallel group, to assess the effect on nerve fibers in patients diagnosed with endometriosis grade III / IV symptomatic ascending-dose oral qui... | ||
| Medical condition: Endometriosis grade III/IV | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
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