- Trials with a EudraCT protocol (74)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
74 result(s) found for: Infertility AND IVF.
Displaying page 4 of 4.
EudraCT Number: 2004-001503-36 | Sponsor Protocol Number: PROT25186 | Start Date*: 2004-11-03 | |||||||||||
Sponsor Name:SERONO ESPAÑA, S.A. | |||||||||||||
Full Title: Lutropin alfa (Luveris) in mid follicular phase for controlled ovarian stimulation (COS) in ovarian ageing: a randomised, comparative with parallel control group, phase II clinical trial. | |||||||||||||
Medical condition: Controlled ovarian stimulation in women with ovarian ageing PT: Assisted Fertilisation | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002993-29 | Sponsor Protocol Number: M13-625 | Start Date*: 2015-07-15 | |||||||||||
Sponsor Name:Abbott Laboratories GmbH | |||||||||||||
Full Title: A Randomized, Open-label, Two-arm, Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg daily versus Crinone 8% intravaginal progesterone gel 90 mg daily ... | |||||||||||||
Medical condition: Treatment for the luteal support in in-vitro fertilization (IVF). | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000105-23 | Sponsor Protocol Number: DYDRA001 | Start Date*: 2019-03-01 |
Sponsor Name:UZ Brussel | ||
Full Title: Oral dydrogesterone (OD) versus micronized vaginal progesterone (MVP) for luteal phase support (LPS) in IVF/ICSI: pharmacokinetics and the impact on the endometrium, the microbiota of the genital t... | ||
Medical condition: Female infertility | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
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: 2022-002310-16 | Sponsor Protocol Number: LHinPOR001 | Start Date*: 2023-02-01 |
Sponsor Name:UZ Brussel | ||
Full Title: Endometrial gene expression profiles during ovarian stimulation with recombinant human FSH with or without the addition of recombinant human LH in genuine poor responders. | ||
Medical condition: Infertility | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002027-42 | Sponsor Protocol Number: POR-ELONVA | Start Date*: 2013-08-14 |
Sponsor Name:INSTITUTO DE INVESTIGACION SANITARIA LA FE | ||
Full Title: PROSPECTIVE AND RANDOMIZED STUDY FOR ASSESSMENT OF CONTROLLED OVARIAN STIMULATION WITH ALFA Corifollitropin IN PATIENTS WITH OVARIAN RESPONSE EXPECTED OR POOR IN VITRO FERTILIZATION CYCLE. | ||
Medical condition: Women who meet the criteria for infertility Bologna | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004669-28 | Sponsor Protocol Number: 1704-GINFER-01-BMEC | Start Date*: 2019-04-04 |
Sponsor Name:CENTRO GINECOLOGICO GINFER | ||
Full Title: A clinical tryal of the utility of ozone in patients with implantation failures | ||
Medical condition: Evaluate the action of ozone in the regulation, concentration and activation of uterine NK. Quantify the cytokines present in the uterine decidua pre and post ozone exposure in the uterus. Quantify... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004966-34 | Sponsor Protocol Number: 38825 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:NV Organon | |||||||||||||
Full Title: A phase III, uncontrolled trial to assess the non-immunogenicity and safety of Org 36286 in patients undergoing repeated controlled ovarian stimulation cycles using a multiple dose GnRH antagonist ... | |||||||||||||
Medical condition: Controlled Ovarian Stimulation (COS) to induce the development of multiple follicles in patients participating in an Assisted Reproductive Technology (ART) program | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) SE (Completed) HU (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004491-17 | Sponsor Protocol Number: REMODEL | Start Date*: 2021-03-31 |
Sponsor Name:UZ Brussel | ||
Full Title: Dydrogesterone versus micronized vaginal progesterone (MVP) for luteal phase support (LPS) in hormone replacement therapy (HRT) frozen embryo transfer (FET) cycles. | ||
Medical condition: progesterone as luteal phase supplementation in frozen embryo transfer cycles | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001105-81 | Sponsor Protocol Number: ACT-CYC-300-2013-01 | Start Date*: 2013-07-31 |
Sponsor Name:Actavis Group PTC ehf. | ||
Full Title: Randomized Clinical Trial to Compare the Pregnancy Rates of Vaginally Applied Cyclogest® Pessary and Crinone® 8% Gel After In-vitro Fertilization | ||
Medical condition: Luteal phase support after IVF | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: HU (Completed) BE (Completed) BG (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-002215-26 | Sponsor Protocol Number: M13-563 | Start Date*: 2013-07-18 | |||||||||||
Sponsor Name:Abbott Laboratories GmbH | |||||||||||||
Full Title: A Double-Blind, Double-Dummy, Randomized, Two-arm, Multicenter Study Comparing the Efficacy, Safety and Tolerability of Oral Dydrogesterone 30 mg daily versus Intravaginal Micronized Progesterone C... | |||||||||||||
Medical condition: Female infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) AT (Completed) ES (Completed) FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003484-56 | Sponsor Protocol Number: BOLDOS-18 | Start Date*: 2019-12-26 | |||||||||||
Sponsor Name:Miguel Caballero Campo | |||||||||||||
Full Title: Efficacy of corifolitropin alfa in double ovarian stimulation compared with two conventional ovarian stimulation cycles for embryo accmulation in low responder patients. Multicenter randomized cont... | |||||||||||||
Medical condition: Infertility in patients requiring in vitro fertilization treatment with poor ovarian response profile, defined by Bologna Criteria. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000993-32 | Sponsor Protocol Number: S55300 | Start Date*: 2013-05-07 | ||||||||||||||||
Sponsor Name:University Hospital Leuven | ||||||||||||||||||
Full Title: Does prolonged GnRH downregulation prior to ART improve the clinical pregnancy rate in postoperative endometriosis patients? A RCT | ||||||||||||||||||
Medical condition: endometriosis, subfertility | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-001045-21 | Sponsor Protocol Number: FSD-MIC-2022-03 | Start Date*: 2023-04-10 |
Sponsor Name:FUNDACION SANTIAGO DEXEUS FONT | ||
Full Title: A Phase III randomized controlled trial comparing the efficacy, safety and tolerability of two formulations of vaginal micronized progesterone. | ||
Medical condition: Infertility | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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