- Trials with a EudraCT protocol (140)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
140 result(s) found for: Physical stimulation.
Displaying page 1 of 7.
EudraCT Number: 2015-005762-28 | Sponsor Protocol Number: 1512-VLC-066-EB | Start Date*: 2016-04-06 |
Sponsor Name:IVI Valencia | ||
Full Title: Analysis of follicular steroid synthesis during controlled ovarian stimulation with recombinant FSH vs HMG in GnRH antagonist cycles | ||
Medical condition: Women undergoing ovarian stimulation for oocyte donation | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-005443-24 | Sponsor Protocol Number: Dex-PKPD/01 | Start Date*: 2013-03-05 |
Sponsor Name:UMCG | ||
Full Title: Development of a pharmacokinetic/pharmacodynamic model of dexmedetomidine, and the effect of repeated auditory stimulation on pharmacodynamics of dexmedetomidine | ||
Medical condition: To develop a PKPD dexmedetomidine model, and to assess the effect of continuous auditory stimulation on dexmedetomidine pharmacodynamics. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005687-97 | Sponsor Protocol Number: NoSIRS | Start Date*: 2013-06-20 |
Sponsor Name:Medtronic Inc. | ||
Full Title: Effects of Transvenous Vagus Nerve Stimulation on Immune Response: a pilot study | ||
Medical condition: Possible future indications: inflammatory conditions in general | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
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: 2012-004263-47 | Sponsor Protocol Number: EMR200104-011 | Start Date*: 2013-03-01 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: Open-label, single-arm, phase IV, multicenter trial to explore the immunogenicity of the liquid formulation of Saizen® in subjects with adult growth hormone deficiency (AGHD) of adult onset | |||||||||||||
Medical condition: Adult Growth Hormone Deficiency | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) SE (Completed) DE (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000804-14 | Sponsor Protocol Number: OPHT-070119 | Start Date*: 2019-05-10 |
Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | ||
Full Title: The effect of hyperoxia and hypoxia on fluorescence lifetime imaging ophthalmoscopy in healthy subjects | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001225-43 | Sponsor Protocol Number: IB-0121 | Start Date*: 2021-06-14 |
Sponsor Name:Instituto Bernabeu | ||
Full Title: Dual Stim comparison of triggers for the second egg collection: Is there any advantage using 3 different methods of trigger for the second egg collection in Dual Stim cycles in predicted low respon... | ||
Medical condition: Patients with predictive indicators of low ovarian response (according to Poseidon criteria) and who undergo double ovarian stimulation (Dual Stim). | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001683-29 | Sponsor Protocol Number: 114464 | Start Date*: 2015-06-03 | ||||||||||||||||
Sponsor Name:GlaxoSmithKline Biologicals | ||||||||||||||||||
Full Title: A Phase 2/3, randomized, controlled, observer-blind, multi-center trial to evaluate the safety and immunogenicity of a two-dose primary vaccination series of monovalent A/Indonesia/5/2005 (H5N1) va... | ||||||||||||||||||
Medical condition: Healthy volunteers (immunization against avian influenza virus A (H5N1) infection) | ||||||||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000013-10 | Sponsor Protocol Number: PR3042 | Start Date*: 2007-03-14 | |||||||||||
Sponsor Name:Pantarhei Bioscience B.V. | |||||||||||||
Full Title: A double-blind, placebo controlled, randomised, comparative 2-way crossover study to determine the effect of concomitant treatment with dehydroepiandrosterone (50 mg) on sexual arousability and the... | |||||||||||||
Medical condition: Sexual dysfunction caused by the use of oral contraceptives | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2023-000462-33 | Sponsor Protocol Number: 171-7151-202 | Start Date*: 2023-04-19 |
Sponsor Name:Intrepid Therapeutics, Inc. | ||
Full Title: An Open Label Evaluation of the Adrenal Suppression Potential and Pharmacokinetic Properties of Cortexolone 17α-Propionate (CB-03-01) Cream Applied Every 12 Hours for Two Weeks in Subjects with Acn... | ||
Medical condition: Facial Acne Vulgaris | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-015867-15 | Sponsor Protocol Number: DBS | Start Date*: 2010-02-18 |
Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | ||
Full Title: Different Anesthesiological Strategies Evaluation in Deep Brain Stimulation Neurosurgeries | ||
Medical condition: Parkinson Desease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004082-42 | Sponsor Protocol Number: OXY-2 | Start Date*: 2005-12-05 |
Sponsor Name:Søren Sindrup, Dept. of Neurology, University Hospital of Odense | ||
Full Title: The Pharmacogenetics of Oxycodone analgesia in human experimental pain models | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-003857-78 | Sponsor Protocol Number: D-CN-52014-244 | Start Date*: 2023-06-29 |
Sponsor Name:Ipsen Pharma | ||
Full Title: A phase III, open-label, multicentre, single arm study to assess the efficacy and safety of the triptorelin 6-month formulation in Chinese paediatric participants with central precocious puberty | ||
Medical condition: Central Precocious Puberty | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2016-000616-15 | Sponsor Protocol Number: CB-03-01/28 | Start Date*: 2016-05-25 | |||||||||||
Sponsor Name:Cassiopea S.P.A. | |||||||||||||
Full Title: An Open Label Evaluation of the Adrenal Suppression Potential and Trough Plasma Concentrations of Cortexolone 17α-Propionate (CB-03-01) Cream Applied Every 12 Hours for Two Weeks in Subjects 9 to <... | |||||||||||||
Medical condition: Acne vulgaris | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (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: 2016-002780-34 | Sponsor Protocol Number: 13VR3 | Start Date*: 2016-11-10 | |||||||||||
Sponsor Name:Versartis, Inc. | |||||||||||||
Full Title: An Open-Label, Long-Term Safety Study of A Long-acting Human Growth Hormone Somavaratan (VRS-317) in Children with Growth Hormone Deficiency The VISTA Study: Versartis Long-Term Safety Study of So... | |||||||||||||
Medical condition: Growth hormone deficiency | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) BE (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-005082-31 | Sponsor Protocol Number: MP-TAP-2016-01 | Start Date*: 2017-11-20 |
Sponsor Name:MRI Research Unit, Radiology Department. Hospital del Mar. | ||
Full Title: Assessment of Tapentadol effects on patients with pain central sensitization using functional MRI | ||
Medical condition: Patients suffering from pain due to knee osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-000137-19 | Sponsor Protocol Number: | Start Date*: 2007-08-07 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Metyrapone as additive treatment in patients with major depression | |||||||||||||
Medical condition: unipolar depressive episode without psychotic features according to DSM-IV-TR | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
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: 2019-002706-46 | Sponsor Protocol Number: DE-3.01_SII-Tdap | Start Date*: 2020-01-09 | |||||||||||
Sponsor Name:Vakzine Projekt Management GmbH | |||||||||||||
Full Title: A Phase II/III, Multicenter, Randomized, Observer-blinded, Active Controlled Clinical Study to Assess the Safety and Immunogenicity of the Tetanus, Diphtheria and Acellular Pertussis Vaccine SIIPL ... | |||||||||||||
Medical condition: Active booster immunization against tetanus, diphtheria and pertussis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
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