- Trials with a EudraCT protocol (83)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
83 result(s) found for: Infertility, Female Infertility, Male Infertility AND Infertility.
Displaying page 1 of 5.
EudraCT Number: 2021-000941-42 | Sponsor Protocol Number: FSD-IEQ-2021-03 | Start Date*: 2021-07-06 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Fundacion Santiago Dexeus Font | ||||||||||||||||||||||||||||||||||||||
Full Title: The impact of the intensity of ovarian stimulation on embryo quality in predicted suboptimal responders. A randomized controlled trial. | ||||||||||||||||||||||||||||||||||||||
Medical condition: To compare the number of GQB and the morphokinetic parameters of early embryo development in infertile suboptimal patients undergoing two different intensities of ovarian stimulation, a milder appr... | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004254-37 | Sponsor Protocol Number: 000400 | Start Date*: 2022-06-27 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled trial to assess the efficacy and safety of FE 999049 for treatment of men with idiopathic infertility | |||||||||||||
Medical condition: Idiopathic male infertility (including oligoasthenozoospermia) | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: SE (Trial now transitioned) DE (Trial now transitioned) ES (Trial now transitioned) DK (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 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 |
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: 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: 2010-023534-23 | Sponsor Protocol Number: EMR 200061-504 | Start Date*: 2011-05-09 | ||||||||||||||||
Sponsor Name:Merck Serono S.A. - Geneva | ||||||||||||||||||
Full Title: A phase IIIB, multicentre, multinational, randomized, open-label trial to compare the efficacy and safety of ovarian stimulation with GONAL-f® day 1 to day 5 followed by Pergoveris® starting day 6 ... | ||||||||||||||||||
Medical condition: Fertility disorders | ||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||
Trial protocol: NL (Completed) SK (Completed) DE (Completed) FI (Completed) GB (Completed) DK (Completed) GR (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-020240-35 | Sponsor Protocol Number: 2010-020240-35 | Start Date*: 2010-07-09 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | ||||||||||||||||||
Full Title: Significance of the FSH receptor polymorphism p.N680S for the efficacy of FSH therapy of idiopathic male infertility: a pharmacogenetic approach. | ||||||||||||||||||
Medical condition: Idiopathic male infertility | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: IT (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
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: 2022-000753-80 | Sponsor Protocol Number: 000298 | Start Date*: 2022-08-04 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, assessor-blind, active-controlled, parallel-group, dose-finding trial to investigate the efficacy and safety of FE 999302 for triggering of final follicular maturation in women underg... | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) CZ (Prematurely Ended) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001785-38 | Sponsor Protocol Number: 000401 | Start Date*: 2021-10-05 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, parallel groups, multicentre, multinational trial comparing the ovarian response of a starting dose of 15 µg follitropin delta (REKOVELLE) to a starting do... | |||||||||||||
Medical condition: Infertility in women undergoing assisted reproductive technologies (ART) such as an in vitro fertilisation (IVF) or intracytoplasmic sperm injection (ICSI) cycle | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) IT (Completed) FR (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002783-40 | Sponsor Protocol Number: 000304 | Start Date*: 2019-07-04 | |||||||||||||||||||||||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||||||||||||||||||||||
Full Title: A randomised, controlled, open label, parallel group, multicentre trial comparing the efficacy and safety of individualised FE 999049 (follitropin delta) dosing, using a long GnRH agonist protocol ... | |||||||||||||||||||||||||||||||||
Medical condition: Infertility in women undergoing assisted reproductive technologies (ART) such as an in vitro fertilisation (IVF) or intracytoplasmic sperm injection (ICSI) cycle | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||||||||||||
Trial protocol: AT (Completed) DK (Completed) NO (Completed) NL (Completed) IT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001950-16 | Sponsor Protocol Number: ISI-2015-1 | Start Date*: 2017-03-03 |
Sponsor Name:Isifer AB | ||
Full Title: A randomized, double blind, controlled, parallel group, multi-centre phase II clinical study of lidocaine pertubation as a treatment for couples with unexplained infertility | ||
Medical condition: Unexplained infertility | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: PL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003788-67 | Sponsor Protocol Number: FS1306 | Start Date*: 2014-01-29 | |||||||||||
Sponsor Name:Watson Laboratories, Inc. - A subsidiary of Actavis, Inc. | |||||||||||||
Full Title: A Randomised, Parallel Group, Assessor-Blind, Multicentre Study to Compare the Safety and Efficacy of Watson rhFSH with Follitropin Alfa (GONAL-f) in Stimulating Multiple Follicular Development in ... | |||||||||||||
Medical condition: Stimulation of multifollicular development in women undergoing superovulation for assisted reproductive technologies (ART) such as in vitro fertilisation (IVF), gamete intra-fallopian transfer and... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) GB (Prematurely Ended) ES (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-001137-41 | Sponsor Protocol Number: 666 | Start Date*: 2018-06-26 |
Sponsor Name:Hvidovre Hospital. Dep of Respiratory Medicine | ||
Full Title: Use of Omalizumab will increase the pregnancy rate, proof of concept study, where women with asthma and infertility will be treated three times with weight and IgE balanced dosis at the sixth day o... | ||
Medical condition: infertility within female asthma patients as a result of systemic inflamation. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000633-36 | Sponsor Protocol Number: 000009 | Start Date*: 2011-08-09 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, parallel groups, multinational, multicentre trial assessing the dose-response relationship of FE 999049 in controlled ovarian stimulation in women undergoi... | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) CZ (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001034-18 | Sponsor Protocol Number: NL43131-018-13 | Start Date*: 2013-09-05 | |||||||||||
Sponsor Name:AMC Amsterdam | |||||||||||||
Full Title: Super ovulation in intrauterine insemination: FSH or Clomifene citrate | |||||||||||||
Medical condition: Women diagnosed with unexplained subfertility or mild male factor subfertility with an indication for intra uterine insemination | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001259-22 | Sponsor Protocol Number: 28613 | Start Date*: 2008-09-01 | |||||||||||
Sponsor Name:Merck Serono International S.A. | |||||||||||||
Full Title: A phase IV prospective, multicentre, randomized, open-label trial to assess the efficacy and safety of GONAL f® at a dose based on subject baseline characteristics determined according to the CONSO... | |||||||||||||
Medical condition: Ovarian stimulation in women undergoing assisted reproductive technology | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) SE (Completed) ES (Completed) DE (Completed) DK (Completed) GB (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001669-17 | Sponsor Protocol Number: 000004 | Start Date*: 2013-09-17 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, controlled, assessor-blind, parallel groups, multicentre, multinational trial comparing the efficacy and safety of FE 999049 with follitropin alfa (GONAL-F) in controlled ovarian stim... | |||||||||||||
Medical condition: Infertility | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) CZ (Completed) DK (Completed) PL (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001590-32 | Sponsor Protocol Number: MMC-2016-01 | Start Date*: 2018-04-19 | |||||||||||
Sponsor Name:Manuel Macía Cortiñas | |||||||||||||
Full Title: Comparison of two protocols of controlled ovarian stimulation with highly purified menotropin in low-responder patients according to Bologna criteria treated in Spanish public hospitals. | |||||||||||||
Medical condition: PRIMARY INFERTILITY | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
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