- Trials with a EudraCT protocol (1,708)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
1,708 result(s) found for: Sperm.
Displaying page 1 of 86.
EudraCT Number: 2009-017940-15 | Sponsor Protocol Number: P081227 | Start Date*: 2010-04-20 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Devenir de la spermatogénèse chez les hommes drépanocytaires traités médicalement (HYDREP). | |||||||||||||
Medical condition: Drépanocytose | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
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: 2007-002859-16 | Sponsor Protocol Number: BXL628 02 17 | Start Date*: 2007-10-10 | |||||||||||
Sponsor Name:BIOXELL SPA | |||||||||||||
Full Title: A randomized, double blind, placebo controlled, parallel group study to determine the effect of Elocalcitol on sperm parameters in infertile male patients | |||||||||||||
Medical condition: male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000402-38 | Sponsor Protocol Number: GS-US-418-4279 | Start Date*: 2018-01-19 | ||||||||||||||||
Sponsor Name:Gilead Sciences, Inc. | ||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Study to Evaluate the Testicular Safety of Filgotinib in Adult Males with Moderately to Severely Active Inflammatory Bowel Disease | ||||||||||||||||||
Medical condition: To evaluate the testicular safety of filgotinib in adult males with moderately to severely Active Inflammatory Bowel Disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) AT (Completed) PT (Prematurely Ended) NL (Prematurely Ended) SE (Prematurely Ended) BE (Prematurely Ended) ES (Prematurely Ended) RO (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-000315-91 | Sponsor Protocol Number: RG_18-236 | Start Date*: 2019-09-09 | |||||||||||
Sponsor Name:University of Birmingham | |||||||||||||
Full Title: The pAToMiUM Trial: pilot trial of Antioxidant Therapy of Men in Unexplained Miscarriage | |||||||||||||
Medical condition: Unexplained miscarriage and how this may relate to the quality of the sperm DNA at conception, with particular emphasis on chromatin structure and DNA fragmentation and whether this may be improved... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003933-14 | Sponsor Protocol Number: GLPG0634-CL-227 | Start Date*: 2019-05-27 | ||||||||||||||||||||||||||
Sponsor Name:Galapagos NV | ||||||||||||||||||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Study to Evaluate the Effect of Filgotinib on Semen Parameters in Adult Males with active Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosin... | ||||||||||||||||||||||||||||
Medical condition: Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis and Non-radiographic Axial Spondyloarthritis | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: LV (Completed) EE (Completed) BG (Completed) BE (Completed) CZ (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000655-24 | Sponsor Protocol Number: CBG-study2 | Start Date*: 2015-04-28 | |||||||||||
Sponsor Name:rigshospitalet | |||||||||||||
Full Title: Denosumab and male infertility: a prospective intervention study | |||||||||||||
Medical condition: Male infertility especially low sperm count | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000722-19 | Sponsor Protocol Number: M12-919 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Single-Arm Study of the Effects of Atrasentan on Spermatogenesis and Testicular Function | |||||||||||||
Medical condition: Diabetic Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020196-23 | Sponsor Protocol Number: EMR 700623-521 | Start Date*: 2011-04-14 | |||||||||||
Sponsor Name:MERCK SERONO SPA | |||||||||||||
Full Title: A phase II, multicentre, open label, prospective, interventional study to evaluate the sperm DNA fragmentation in idiopathic male infertility before and after treatment with Gonal-f PEN 900 IU. | |||||||||||||
Medical condition: Idiophatic male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005315-26 | Sponsor Protocol Number: A25165 | Start Date*: 2008-07-01 | |||||||||||
Sponsor Name:CONRAD, Eastern Virgina Medical School | |||||||||||||
Full Title: Sperm Suppression and Contraceptive Protection provived by Norethisterone Enantate (NET-EN) combined with Testosterone Undecanoate (TU) in healthy men. | |||||||||||||
Medical condition: The proposed study is designed to evaluate whether the combination of a progestin, norethisterone enantate (NET-EN), and an androgen, testosterone undecanoate (TU), represents a safe and effective ... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) IT (Temporarily Halted) GB (Temporarily Halted) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001258-25 | Sponsor Protocol Number: MK8962-031-00 | Start Date*: 2012-11-29 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A phase III, multi-center, open label, uncontrolled trial to investigate the efficacy and safety of MK-8962 (corifollitropin alfa) in combination with human Chorionic Gonadotropin (hCG) in inducing... | |||||||||||||
Medical condition: Hypogonadotropic hypogonadism (HH) in males may result from either absent or inadequate gonadotropin-releasing hormone (GnRH) secretion by the hypothalamus or failure of pituitary gonadotropin secr... | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) IT (Completed) GB (Completed) PL (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-006105-40 | Sponsor Protocol Number: COQ10INF | Start Date*: 2006-06-05 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERO UNIVERSITARIA OSPEDALI RIUNITI UMBERTO I - G.M.LANCISI - G.SALESI | |||||||||||||
Full Title: TREATMENT OF IDIOPATHIC ASTHENOZOOSPERMIE WITH COENZYME Q10. A DOUBLE BLIND CONTROLLED STUDY | |||||||||||||
Medical condition: IDIOPATHIC ASTHENOZOOSPERMIA | |||||||||||||
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Population Age: | Gender: Male | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002521-19 | Sponsor Protocol Number: FSH_IMEN | Start Date*: 2015-10-19 | |||||||||||
Sponsor Name:Instituto de Investigación Sanitaria La Fe | |||||||||||||
Full Title: "Pilot study on the effect of FSH treatment in epigenetic characteristics of sperm in infertile patients with severe oligozoospermia" | |||||||||||||
Medical condition: Male infertility | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004391-36 | Sponsor Protocol Number: AC-052-402 | Start Date*: 2005-05-23 |
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
Full Title: A multicenter, open-label, single-arm safety study to investigate the effects of chronic TRACLEER® treatment on testicular function in male patients with pulmonary arterial hypertension | ||
Medical condition: Many endothelin receptor antagonists have profound effects on the histology and function of the testes in animals. These drugs have been shown to induce atrophy of the seminiferous tubules of the t... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: HU (Completed) CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002498-36 | Sponsor Protocol Number: CCN017 | Start Date*: 2018-10-12 | |||||||||||
Sponsor Name:National Institutes of Health - Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) | |||||||||||||
Full Title: Clinical Evaluation of Daily Application of Nestorone® (NES) and Testosterone (T) Combination Gel for Male Contraception | |||||||||||||
Medical condition: As the clinical trial is intended to investigate a new contraceptive medicinal product, the trial subjects included are not characterized by a specific medical condition. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
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: 2006-003811-36 | Sponsor Protocol Number: 107012 | Start Date*: 2007-01-03 |
Sponsor Name:NV Organon | ||
Full Title: A phase III, randomized, double-blind, active-controlled, equivalence clinical trial to investigate the efficacy and safety of a single injection of 100 µg Org 36286 (corifollitropin alfa) to induc... | ||
Medical condition: Controlled Ovarian Stimulation (COS) to induce the development of multiple follicles in patients participating in an Assisted Reproductive Technology (ART) program | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) AT (Completed) DK (Completed) CZ (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-003006-27 | Sponsor Protocol Number: GEXGP24201 | Start Date*: 2012-11-27 | |||||||||||
Sponsor Name:Glycotope GmbH | |||||||||||||
Full Title: A Phase II, Multicentre, Multinational, Randomised, Assessor-Blind Trial to Investigate the Efficacy and Safety of Various Dosages of FSH-GEX™ in Comparison With 150 IU Gonal-f® in Women Undergoing... | |||||||||||||
Medical condition: women undergoing intracytoplasmatic sperm injection (ICSI) as part of assisted reproduction | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: HU (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
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: 2006-000481-37 | Sponsor Protocol Number: 142003 | Start Date*: 2006-09-07 |
Sponsor Name:NV Organon | ||
Full Title: A randomized, open-label clinical trial to identify predictive factors for controlled ovarian stimulation using a fixed daily dose of 200 IU of recombinant FSH in a GnRH antagonist regimen with or ... | ||
Medical condition: Controlled Ovarian Stimulation (COS) to induce the development of multiple follicles in patients participating in an Assisted Reproductive Technology (ART) program | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: DK (Completed) DE (Completed) FR (Prematurely Ended) ES (Completed) | ||
Trial results: View results |
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