- Trials with a EudraCT protocol (42)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
42 result(s) found for: Antral.
Displaying page 1 of 3.
| EudraCT Number: 2009-012222-36 | Sponsor Protocol Number: 1.0 | Start Date*: 2009-07-23 |
| Sponsor Name:Medizinische Universität Wien, Bernhard Gottlieb Universitätszahnklinik | ||
| Full Title: Verification of an oro-antral communication after tooth extraction in the upper jaw. A Pilot-study | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001143-59 | Sponsor Protocol Number: IVFAFC1 | Start Date*: 2006-07-14 |
| Sponsor Name:School of Human Development | ||
| Full Title: A prospective, randomised study comparing two fixed daily doses (150 IU versus 225 IU) of recombinant FSH for ovarian stimulation during in-vitro fertilisation treatment in predicted low and interm... | ||
| Medical condition: Infertility needing In-Vitro fertilisation treatment | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-004075-41 | Sponsor Protocol Number: 2020-6941 | Start Date*: 2021-02-04 |
| Sponsor Name:Radboudumc | ||
| Full Title: Effectiveness of Somatostatin Analogues in patients with Gastric antral vascular ectasia and symptomatic gastrointestinal bleeding: SAGAVE-Pilot study | ||
| Medical condition: Gastric Antral Vascular Ectasia (also known as watermelon stomach) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-003492-35 | Sponsor Protocol Number: MED2-201301 | Start Date*: 2015-05-26 |
| Sponsor Name:University of Bonn | ||
| Full Title: Prevention of Silent Cerebral Thromboembolism by Oral Anticoagulation with Dabigatran after Pulmonary Vein Isolation for Atrial Fibrillation | ||
| Medical condition: atrial fibriallation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-002453-26 | Sponsor Protocol Number: 73908 | Start Date*: 2020-11-18 | |||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||
| Full Title: Eight weeks of androgen priming by hCG before IVF/ICSI in women with low ovarian reserve. | |||||||||||||
| Medical condition: Female Infertility | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019287-37 | Sponsor Protocol Number: FIN3001 | Start Date*: 2010-08-24 |
| Sponsor Name:Finox AG | ||
| Full Title: A phase III assessor-blinded randomised parallel group multi-centre study to compare efficacy adn safety of two r-hFSH formulations (AFOLIA and Gonal-f®) in women for assisted reproductive treatment | ||
| Medical condition: Stimulation of multifollicular develoment in patients undergoing assisted reproductivet treatment | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DE (Completed) AT (Completed) ES (Completed) GB (Prematurely Ended) DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-003104-11 | Sponsor Protocol Number: 1.0 | Start Date*: 2005-10-11 |
| Sponsor Name:Fertility clinic Odense University Hospital | ||
| Full Title: Androgen priming in the late luteal phase as a mean to improve the outcome of ovarian stimulation for IVF in normogonadotrophic women with a previously proven poor response | ||
| Medical condition: Hypothesis. By combining pituitary downregulation with aromatase inhibitor, and hCG injection during a late luteal phase a powerful stimulation of thecal androgen production is achieved. Thereby, i... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DK (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-002341-30 | Sponsor Protocol Number: 1705-VLC-030-JG | Start Date*: 2017-09-11 | |||||||||||
| Sponsor Name:INSTITUTO VALENCIANO DE INFERTILIDAD (IVI) | |||||||||||||
| Full Title: Usefulness of medroxyprogesterone acetate in the follicular phase for ovarian donors to prevent premature luteinization | |||||||||||||
| Medical condition: prevent premature luteinitation | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-001343-44 | Sponsor Protocol Number: IB-0319-002 | Start Date*: 2019-05-21 |
| Sponsor Name:Instituto Bernabeu | ||
| Full Title: Conventional ovarian stimulation vs. stimulation with single injection of Corifollitropin alfa in oocyte donors. Randomized clinical trial. Tail Studio | ||
| Medical condition: Oocyte donation | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000971-17 | Sponsor Protocol Number: 58335 | Start Date*: 2019-07-17 |
| Sponsor Name:UZ Brussel | ||
| Full Title: Double trigger and ovum retrieval vs. conventional antagonist ovarian stimulation protocol in poor prognosis women undergoing IVF/ICSI: A pilot study | ||
| Medical condition: infertility | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-000228-24 | Sponsor Protocol Number: MANA2016-1 | Start Date*: 2016-07-13 |
| Sponsor Name:UZ Brussel | ||
| Full Title: Eradication of H. pylori infection in Belgium: bismuth versus first line therapy | ||
| Medical condition: Patients with H. pylori infection, never treated before | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-004969-40 | Sponsor Protocol Number: RHFERAMH-0001 | Start Date*: 2012-11-27 | |||||||||||
| Sponsor Name:Fertility Clinic, Copenhagen University Hospital, Rigshospitalet | |||||||||||||
| Full Title: An AMH based indivdualised controlled ovarian stimulation regiment using Corifollitrophin or graded doses of rFSH versus a standard protocol. A randomised controlled trial | |||||||||||||
| Medical condition: In vitro fertilization include controlled ovarian stimulation (COS), where follicles are stimulated to full maturity. One of the main problems of the IVF treatment is still to some patients deve... | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2020-005914-16 | Sponsor Protocol Number: 2019COIMBRA001 | Start Date*: 2021-03-01 | |||||||||||
| Sponsor Name:Universitair Ziekenhuis Brussel | |||||||||||||
| Full Title: COmbining Interventions of fertility preservation to Mitigate fertility loss after BReAst cancer | |||||||||||||
| Medical condition: Female patients with breast cancer | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-002979-17 | Sponsor Protocol Number: MANCOR | Start Date*: 2014-01-27 |
| Sponsor Name:IVI Sevilla | ||
| Full Title: Comparative study between the usage of corifollitropin alfa and daily recombinant FSH in the ovarian stimulation of low responders | ||
| Medical condition: Low response to ovarian stimulation | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001743-20 | Sponsor Protocol Number: 1403-MAD-013-AR | Start Date*: 2015-07-30 |
| Sponsor Name:IVI Madrid | ||
| Full Title: A Multicentre, prospective, randomised clinical trial comparing the cost and efficacy of corifolitropina alfa vs Recombinant FSH and / or HP-hMG | ||
| Medical condition: The study is proposed to determine the level of compliance and pharmacoeconomic impact of three protocols for controlled ovarian stimulation in women participating in oocyte donation program | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-022151-32 | Sponsor Protocol Number: FUNDEX001 | Start Date*: 2011-02-03 |
| Sponsor Name:FUNDACION SANTIAGO DEXEUS FONT | ||
| Full Title: Ensayo clínico fase II aleatorizado de cotratamiento con hormona de crecimiento recombinante humana dentro de un protocolo largo de estimulación ovárica bajo agonista de GnRH en mujeres con pobre r... | ||
| Medical condition: Comprobar si la adición de rGH a un tratamiento estándar de estimulación ovárica controlada mejora la respuesta ovárica en mujeres con pobre respuesta previa. Los objetivos secundarios incluyen la... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-000201-11 | Sponsor Protocol Number: VLC-CB-090108-001 | Start Date*: 2008-05-30 | |||||||||||
| Sponsor Name:Instituto Valenciano de Infertilidad | |||||||||||||
| Full Title: Ensayo piloto randomizado, doble-ciego, en grupos paralelos, placebo-controlado, monocéntrico evaluando la tolerabilidad de la quinagolida 200mcg/día en un régimen de aumento de dosis en donantes d... | |||||||||||||
| Medical condition: Pacientes con riesgo del Sindrome de Hiperestimulación Ovárica (SHO) | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-002425-21 | Sponsor Protocol Number: 11054 | Start Date*: 2012-02-10 |
| Sponsor Name:University of Nottingham | ||
| Full Title: Efficacy of Dehydroepiandrosterone to overcome the effect of ovarian aging | ||
| Medical condition: Women having low ovarian reserve undergoing IVF/ICSI treatment | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-009429-26 | Sponsor Protocol Number: local 997 (P06034) | Start Date*: 2010-03-15 |
| Sponsor Name:FREE UNIVERSITY OF BRUSSELS | ||
| Full Title: A PILOT STUDY TO EVALUATE THE EFFECT OF TRIGGERING FINAL OOCYTE MATURATION WITH GnRHa OR hCG ON ENDOMETRIAL RECEPTIVITY PARAMETERS AND THE LUTEAL PHASE IN OOCYTE DONORS | ||
| Medical condition: Compare the endometrium of oocyte donors, who had final oocyte maturation with either hCG, Suprefact, followed by hCG 35 hours after triggering, Suprefact or Suprefact without luteal phase support.... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
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