- 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 1 of 4.
EudraCT Number: 2017-002936-17 | Sponsor Protocol Number: LIV001 | Start Date*: 2019-02-22 |
Sponsor Name:Livio Falun | ||
Full Title: Treatment with intralipid in assisted fertilization | ||
Medical condition: Infertility conditions that required IVF treatment Male infertility Endometrosis PCOS uNEXPLAINED INFERTILITY Tubal damage | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001708-39 | Sponsor Protocol Number: S54224 | Start Date*: 2012-06-07 | ||||||||||||||||
Sponsor Name:University Hospital Leuven | ||||||||||||||||||
Full Title: Prospective randomized trial concerning three different stimulation methods in IVF/ICSI treatment in poor responders | ||||||||||||||||||
Medical condition: Subfertility | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-009375-35 | Sponsor Protocol Number: rFSH+rhCG/rFSH+rLH | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:Regionshospital skive | |||||||||||||
Full Title: Den endokrine effekt af enten r-LH eller lav dosis r-hCG tilskud til r-FSH stimulering hos normogonadotrope kvinder som gennemgår IVF/ICSI behandling efter en lang GnRH agonist nedreguleringsprotocol | |||||||||||||
Medical condition: Fertilitetsbehandling. Sammenligne de endokrine effekter, specielt E2 niveau på hCG dagen hos normogonadatrope IVF/ICSI patienter, som får tilskud af LH aktivitet i form af enten rhCG eller rLH | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003304-39 | Sponsor Protocol Number: 13.010 | Start Date*: 2014-07-16 | |||||||||||
Sponsor Name:Fertilitycenter Odense | |||||||||||||
Full Title: Assisted reproduction and the early luteal phase The effect of ovulation induction on the endocrine profile | |||||||||||||
Medical condition: Infertility, particularly the luteal phase during IVF | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005409-22 | Sponsor Protocol Number: FRAGMIN | Start Date*: 2007-09-03 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA UNIVERSITARIA CAREGGI | |||||||||||||
Full Title: RANDOMIZED MULTICENTER STUDY ON DALTEPARIN TREATMENT IN IVF PATIENTS | |||||||||||||
Medical condition: couple infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000448-13 | Sponsor Protocol Number: Agonist6 | Start Date*: 2014-04-23 | |||||||||||
Sponsor Name:The Fertility Clinic, Skive Regional Hospital | |||||||||||||
Full Title: The exogenous progesterone free luteal phase after GnRHa trigger – a randomized controlled pilot study in high-responder IVF patients | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005208-24 | Sponsor Protocol Number: hCG-GR-001-2016 | Start Date*: 2017-07-12 | |||||||||||
Sponsor Name:Prof. Harry Siristatidis | |||||||||||||
Full Title: A prospective, multicenter, double-blind, randomized, placebo-controlled, two-parallel groups Phase IIIb clinical study, to assess the efficacy and safety of adding low doses of hCG at a short IVF ... | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001124-20 | Sponsor Protocol Number: PCOS-5 | Start Date*: 2005-04-18 |
Sponsor Name:Sigrun Kjøtrød | ||
Full Title: Metformin treatment before IVF/ICSI in normal weight women with polycystic ovarian syndrome. A European, prospective, randomised, double blind, multicenter study. | ||
Medical condition: Polycystic ovary syndrome (PCOS) is a disorder characterized by polycystic ovaries, oligo-amenorrhea and hyperandrogenism. It is the most common endocrine disorder in women of fertile age. PCOS wom... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) SE (Completed) FI (Completed) GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019411-37 | Sponsor Protocol Number: FE999906CS11 | Start Date*: 2010-08-30 | |||||||||||
Sponsor Name:FERRING Arzneimittel GmbH | |||||||||||||
Full Title: A Prospective, Open Label, Randomised, Parallel Group Trial Comparing the Effects of Highly Purified Menotrophin and Recombinant Follicle Stimulating Hormone (rFSH, Follitropin alpha) Administered ... | |||||||||||||
Medical condition: Controlled ovarian hyperstimulation to induce the development of multiple follicles for assisted reproductive technologies | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001622-10 | Sponsor Protocol Number: 000048 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, placebo-controlled, double-blind, parallel groups, multinational, multicentre trial assessing the effect of barusiban administered subcutaneously on the day of transfer on implantatio... | |||||||||||||
Medical condition: Infertility female | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001248-22 | Sponsor Protocol Number: 95576471 | Start Date*: 2006-02-21 |
Sponsor Name:Fertilitetsklinikken Nordica | ||
Full Title: A prospective randomized multicentre study to compare Crinone 8% once daily versus other vaginal progesterone. | ||
Medical condition: Luteal support in connnection with IVF treatment. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-003451-42 | Sponsor Protocol Number: 19642021 | Start Date*: 2021-12-23 | |||||||||||
Sponsor Name:Dept. of Growth and Reproduction | |||||||||||||
Full Title: FITMI - First In Treating Male Infertility | |||||||||||||
Medical condition: Male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005682-24 | Sponsor Protocol Number: RIOTA2015 | Start Date*: 2016-03-16 | |||||||||||||||||||||
Sponsor Name:Sven Olaf Skouby, Professor, MD, DMSc. Unit of Reproductive Medicine, Herlev/Gentofte Hospital | |||||||||||||||||||||||
Full Title: REDUCING THE IMPACT OF OVARIAN STIMULATION - THE RIOT PROJECT STUDY RIOT A: THE ROLE OF AROMATASE INHIBITOR IN REDUCING THE DETRIMENTAL EFFECTS OF OVARIAN STIMULATION TO OPTIMIZE OUTCOMES IN FRESH... | |||||||||||||||||||||||
Medical condition: Infertility | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-005145-23 | Sponsor Protocol Number: 53736 | Start Date*: 2017-08-29 | |||||||||||||||||||||
Sponsor Name:DIPARTIMENTO DI SCIENZE CHIRURGICHE - UNIVERSITà DEGLI STUDI DI TORINO | |||||||||||||||||||||||
Full Title: Prospective randomized trial comparing corifollitropin alfa (CF-alfa) late start (day 4) vs. CF-alfa standard start (day2) in poor, normal and potential high-responders undergoing IVF/ICSI | |||||||||||||||||||||||
Medical condition: Women with low reproductive capacity | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004954-27 | Sponsor Protocol Number: | Start Date*: 2012-12-07 | |||||||||||
Sponsor Name:Clinical Trials and Research Governance, University of Oxford | |||||||||||||
Full Title: A single centre open-label randomised controlled trial of long term pituitary down-regulation before in vitro fertilisation for women with endometriosis: a pilot study | |||||||||||||
Medical condition: Sub-infertility due to endometriosis | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005683-41 | Sponsor Protocol Number: RIOTB2015 | Start Date*: 2016-03-16 | |||||||||||||||||||||
Sponsor Name:Sven O. Skouby, Professor, MD, DMSc. Unit of reproductive Medicine, Herlev/Gentofte Hospital | |||||||||||||||||||||||
Full Title: REDUCING THE IMPACT OF OVARIAN STIMULATION - THE RIOT PROJECT RIOT STUDY B: MAPPING THE ENDOCRINE DETERMINANTS OF OVARIAN STIMULATION TO OPTIMIZE OUTCOMES IN FRESH EMBRYO TRANSFER CYCLES ... | |||||||||||||||||||||||
Medical condition: Infertility | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-008355-42 | Sponsor Protocol Number: 2008-257 | Start Date*: 2009-01-27 | |||||||||||
Sponsor Name:Fertilitetsklinikken | |||||||||||||
Full Title: Supplering med hCG ved kontrolleret ovariel stimulering med rekombinant FSH for in vitro fertilisering Et randomiseret kontrolleret klinisk studie Kliniske, embryonale, endokrine og genetiske aspek... | |||||||||||||
Medical condition: Dette studie er et investigator initieret randomiseret og kontrolleret hCG ”dose-finding” studie, hvor Predalon (hCG) vil blive anvedt som supplering i forskellige doser til stimulationsbehandling... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000447-32 | Sponsor Protocol Number: Agonist5 | Start Date*: 2014-04-23 | |||||||||||
Sponsor Name:The Fertility Clinic, Skive regional Hospital | |||||||||||||
Full Title: The exogenous progesterone free luteal phase after GnRHa trigger – a randomized controlled pilot study in normo-responder IVF patients | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001174-33 | Sponsor Protocol Number: 28612 | Start Date*: 2008-12-30 | |||||||||||
Sponsor Name:Merck Serono International S.A., A branch of Laboratoires Serono S.A. | |||||||||||||
Full Title: A mulitnational, multicenter, exploratory pharmacogenomics trial to test the importance of identified genetic markers, and potentially identify new markers of various ovarian responses to GONAL-f® ... | |||||||||||||
Medical condition: Females undergoing assisted reproductive technology (ART), in vitro fertilisation (IVF) or intra cytoplasmic sperm injection (ICSI) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) FR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-003810-13 | Sponsor Protocol Number: 000289 | Start Date*: 2018-05-21 | |||||||||||||||||||||||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||||||||||||||||||||||
Full Title: A randomised, double-blind, placebo-controlled, parallel-group, dose-range trial to investigate the efficacy and safety of FE 999302 as add-on treatment to follitropin delta (REKOVELLE) in women un... | |||||||||||||||||||||||||||||||||
Medical condition: Women diagnosed with tubal infertility or unexplained infertility or endometriosis stage I/II or having partners diagnosed with male factor infertility, eligible for IVF and/or ICSI. | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: CZ (Completed) DK (Completed) BE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
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