- Trials with a EudraCT protocol (529)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
529 result(s) found for: Light therapy.
Displaying page 1 of 27.
EudraCT Number: 2005-004640-31 | Sponsor Protocol Number: TUD-Akne02-003 | Start Date*: 2006-02-15 |
Sponsor Name:Technische Universität Dresden | ||
Full Title: Control of therapy of acne papulopustulosa by visible light with waterfiltered infrared and / or Adapalen (Differin Gel) | ||
Medical condition: Acne papulopustulos | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2008-006497-15 | Sponsor Protocol Number: LD | Start Date*: 2009-10-14 |
Sponsor Name:Wilhelminen Krebsforschung GmbH | ||
Full Title: Lenalidomide and Dexamethasone for treatment of patients with acute myeloma (light chain)-induced renal failure | ||
Medical condition: There are two patient groups to be included into the study: 1) Patients with previously unknown MM and acute light chain induced renal failure 2) Patients with previously diagnosed MM, normal or... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) CZ (Completed) SK (Completed) DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000220-18 | Sponsor Protocol Number: C.2524.0472.01 | Start Date*: 2013-03-25 |
Sponsor Name:University of Amsterdam | ||
Full Title: Effects of melatonin treatment, light therapy, and sleep improvement on psychosocial, cognitive, and behavioural outcomes in children with Delayed Sleep Phase Syndrome and their parents | ||
Medical condition: Delayed Sleep Phase Syndrome | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003473-42 | Sponsor Protocol Number: 14086 | Start Date*: 2016-06-16 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: Home Interventions and Light therapy for the treatment of vitiligo | |||||||||||||
Medical condition: Vitiligo | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006012-31 | Sponsor Protocol Number: 29-11-2011version1 | Start Date*: 2012-02-06 | |||||||||||
Sponsor Name:Bispeberg Hospital | |||||||||||||
Full Title: Reducing light sensitivity after photodynamic therapy | |||||||||||||
Medical condition: Sun damage skin | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005986-36 | Sponsor Protocol Number: 7977 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:University of Bergen | |||||||||||||
Full Title: DELAYED SLEEP PHASE SYNDROME. SLEEP, PERSONALITY, DEVELOPMENTAL HISTORY, CIRCADIAN RHYTHM AND TREATMENT | |||||||||||||
Medical condition: Delayed sleep phase syndrome - DSPS. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005483-10 | Sponsor Protocol Number: DPIP-2012-02 | Start Date*: 2013-05-01 | |||||||||||
Sponsor Name:University College Dublin | |||||||||||||
Full Title: Dipeptidyl peptidase-4 Inhibition and Narrow-band Ultraviolet-B light in Psoriasis (DINUP): A Randomised Clinical Trial. | |||||||||||||
Medical condition: Psoriasis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004633-15 | Sponsor Protocol Number: BAY38-9456/12496 | Start Date*: 2007-01-24 | |||||||||||
Sponsor Name:BAYER Vital GmbH | |||||||||||||
Full Title: A randomized, double-blind, parallel group prospective pilot study to assess the effect of vardenafil on clinical outcome and on procedure duration after green light laser-ablation of the prostate ... | |||||||||||||
Medical condition: The objective of this study is to compare the impact of vardenafil application vs. placebo on green light laser ablation of the prostate in patients presenting with benign prostate hyperplasia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002663-42 | Sponsor Protocol Number: TFDTRASP | Start Date*: 2015-11-13 |
Sponsor Name:ClĂnica Universidad de Navarra/Universidad de Navarra | ||
Full Title: RANDOMISED PILOT STUDY TO ASSESS THE CLINICAL EFFICACY OF DAYLIGHT PHOTODYNAMIC THERAPY WITH METHYL AMINOLEVULINATE CREAM (METVIX?), (MAL-PDT), IN THE PREVENTION OF ACTINIC KERATOSIS AND NON MELANO... | ||
Medical condition: Actinic Keratosis (AK) are histologically characterized by the proliferation of keratinocytes with atypical cytology in the epidermis. One of the main risk factors for its occurrence is immunosuppr... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002976-32 | Sponsor Protocol Number: unknown | Start Date*: 2007-09-06 |
Sponsor Name:TIPharma | ||
Full Title: COBRA-light study, an open randomised trial comparing a modified COBRA therapy with the COBRA therapy according to BeSt in early rheumatoid arthritis. | ||
Medical condition: Patients with early rheumatoid arthritis wil be treated with a combination therapy: COBRA according to BEST or a modified COBRA schedule (COBRA-light). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-018313-29 | Sponsor Protocol Number: PPA/904A/001 | Start Date*: 2010-03-23 | |||||||||||
Sponsor Name:Photopharmica | |||||||||||||
Full Title: Open-label, within-subject controlled, Phase IIa study to investigate repeat dose antimicrobial photodynamic therapy in patients with acne vulgaris. | |||||||||||||
Medical condition: Acne vulgaris | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-004318-14 | Sponsor Protocol Number: NEOD001-201 | Start Date*: 2016-06-13 | |||||||||||
Sponsor Name:Prothena Therapeutics Limited | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-blind, Placebo-controlled Study of NEOD001 in Previously Treated Subjects with Light Chain (AL) Amyloidosis who have Persistent Cardiac Dysfunction | |||||||||||||
Medical condition: Light chain (AL) amyloidosis involves a hematologic disorder caused by clonal plasma cells that produce misfolded immunoglobulin light chains. Overproduction of misfolded light chains results in bo... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) GB (Completed) GR (Completed) ES (Prematurely Ended) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000459-88 | Sponsor Protocol Number: PDT08 | Start Date*: 2008-12-09 |
Sponsor Name:Univ.-Prof. Dr. Hans F. Merk, Dept. of Dermatology, University Hospital, RWTH Aachen University | ||
Full Title: Prospective, randomized study of the efficacy of photodynamic therapy in actinic keratosis | ||
Medical condition: We treat patients with superficial actinic keratosis grade I-II on the face or scalp. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002746-50 | Sponsor Protocol Number: Q272dnro47/2014 | Start Date*: 2014-09-19 |
Sponsor Name:Mari Salmivuori | ||
Full Title: Superficial basal cell cancer's photodynamic therapy: comparing three photosensitises: hexylaminolevulinate versus methylaminolevulinate and aminolevulinic acid nano emulsion versus methylaminolev... | ||
Medical condition: Superficial basal cell carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000475-25 | Sponsor Protocol Number: SPON489-07 | Start Date*: 2009-11-10 |
Sponsor Name:Cardiff University | ||
Full Title: Randomised, controlled, double-blind, parallel group clinical trial evaluating the efficacies and safety of methyl-aminolevulinate photodynamic therapy and intense pulsed light, administered as pl... | ||
Medical condition: Mild to moderate acne vulgaris in adult patients. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004796-40 | Sponsor Protocol Number: 2018_58 | Start Date*: 2020-06-11 |
Sponsor Name:CHU de Lille | ||
Full Title: Multicenter Phase II study with dose-light escalation, intraoperative glioblastoma photodynamic therapy | ||
Medical condition: Glioblastoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) BE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003949-32 | Sponsor Protocol Number: A6281287 | Start Date*: 2007-12-21 | |||||||||||
Sponsor Name:Pfizer Ltd. Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK | |||||||||||||
Full Title: A two-year multi-centre, randomized two arm study of Genotropin treatment in very young children born small for gestational age: Early Growth and Neurodevelopment (EGN) | |||||||||||||
Medical condition: Short Stature children born small for Gestational Age (SGA) | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) BE (Completed) ES (Completed) AT (Completed) GB (Completed) FR (Completed) IT (Completed) DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005017-12 | Sponsor Protocol Number: EyeADHD-01 | Start Date*: 2014-03-31 | |||||||||||
Sponsor Name:Parnassia Bavo Groep - PsyQ | |||||||||||||
Full Title: Looking into the eye of ADHD. Investigating the relationship between ADHD, the delayed circadian rhythm and the functioning of the eye. | |||||||||||||
Medical condition: Adults with ADHD and suboptimal eye functioning. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004304-39 | Sponsor Protocol Number: A6281283 | Start Date*: 2008-03-12 | |||||||||||
Sponsor Name:Pfizer Pharma GmbH | |||||||||||||
Full Title: NEUROMUSCULAR CHANGES IN SMALL FOR GESTATIONAL AGE (SGA-) CHILDREN DURING SOMATROPIN THERAPY - A PROSPECTIVE, RANDOMIZED, CONTROLLED, OPEN-LABEL, MULTICENTER TRIAL (SGA-POWER STUDY) | |||||||||||||
Medical condition: Growth disturbance (current height SDS < -2.5 and parental adjusted height SDS < -1) in short children born small for gestational age (SGA), with a birth weight and/or length below -2 SD, who faile... | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004089-33 | Sponsor Protocol Number: CHDR1317 | Start Date*: 2013-11-26 |
Sponsor Name:Centre for Human Drug Research | ||
Full Title: A Phase 1, Open Label, Exploratory Study for the Intra-operative Imaging of Folate Receptor Alpha Positive Ovarian and Lung Cancer using the Tumor Specific Imaging Agent EC17 | ||
Medical condition: primary ovarian carcinoma and primary non small cell lung carcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
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