- Trials with a EudraCT protocol (630)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
630 result(s) found for: Affection.
Displaying page 1 of 32.
EudraCT Number: 2016-002835-14 | Sponsor Protocol Number: SCCCSH01 | Start Date*: 2016-10-07 | |||||||||||
Sponsor Name:Nordsjællands Hospital Hillerød | |||||||||||||
Full Title: Supraclavicular catheter for regional anesthesia of the shoulder - an explorative study in healthy volunteers. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012398-36 | Sponsor Protocol Number: a003c | Start Date*: 2009-06-18 | |||||||||||||||||||||
Sponsor Name:Helsinki University Hospital | |||||||||||||||||||||||
Full Title: Patient-controlled sedation with propofol in ERCP:alfentanyl vs remifentanyl | |||||||||||||||||||||||
Medical condition: Billiar tract and pancreatic disoderes | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000271-42 | Sponsor Protocol Number: 11012007 | Start Date*: 2007-05-08 | |||||||||||
Sponsor Name:Matti Eskelinen | |||||||||||||
Full Title: OKSIKODONIN ANALGEETTINEN PITOISUUS PLASMASSA YHDESSÄ PARASETAMOLIN 1g TAI 2g IV KANSSA ANNETTUNA MAHAKIRURGISILLA POTILAILLA | |||||||||||||
Medical condition: Tutkimukseen otetaan 24 sappileikkaukseen tulevaa perustervettä aikuispotilasta. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000810-44 | Sponsor Protocol Number: FSJD-PMM2-2016 | Start Date*: 2017-05-31 | |||||||||||
Sponsor Name:Fundació Sant Joan de Déu | |||||||||||||
Full Title: Phase II clinical trial to evaluate the effectiveness and safety of acetazolamide in the treatment of cerebellar syndrome in patients with PMM2-CDG deficiency. | |||||||||||||
Medical condition: Cerebellar syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002398-22 | Sponsor Protocol Number: CL-070-II-01 | Start Date*: 2005-01-27 | |||||||||||
Sponsor Name:IDEA AG | |||||||||||||
Full Title: Double-blind, placebo-controlled study to investigate the efficacy and safety of IDEA-070 (ketoprofen in Transfersome®) in different dermatological diseases | |||||||||||||
Medical condition: Patients with different dermatological diseases Atopic eczema (MedDRA 6.0, LLT: 10003641) Dishydrotic hand eczema (MedDRA 6.0, LLT: 10013913) Plaque type psoriasis (MedDRA 6.0, LLT: 10050576)... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004316-23 | Sponsor Protocol Number: CLOMG | Start Date*: 2004-11-12 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Randomised, controlled , double blind trial on emodinamic, analgesic, pharmacoeconomic effects of clonidine and magnesium in premedication of laparoscopic surgery for colecitis ablation. | |||||||||||||
Medical condition: Post operative analgesia. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004601-32 | Sponsor Protocol Number: SM4-UG-14 | Start Date*: 2015-01-07 | |||||||||||
Sponsor Name:Gentofte Hospital | |||||||||||||
Full Title: The Effect of Local Anesthetic Volume within the Adductor Canal on Quadriceps Function Evaluated by Electromyography: A Randomized, Observer-Masked, Placebo-Controlled Study in Volunteers. | |||||||||||||
Medical condition: Healthy volunteers. Results will be used for optimizing the treatment of post-operative pain after total knee arthroplasty | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002184-26 | Sponsor Protocol Number: 2012/176/HP | Start Date*: 2014-01-20 | |||||||||||
Sponsor Name:CHU de Rouen | |||||||||||||
Full Title: Efficacy of parietal continous infiltration of local anesthesic on diaphragmatic function after upper abdominal surgery through a subcostal incision | |||||||||||||
Medical condition: Diaphragmatic function after upper abdominal surgery through a subcostal incision | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007968-42 | Sponsor Protocol Number: a001c | Start Date*: 2009-02-13 | |||||||||||||||||||||||||||||||
Sponsor Name:Helsinki University Central Hospital | |||||||||||||||||||||||||||||||||
Full Title: Patient-controlled sedation vs propofol infusion for ERCP | |||||||||||||||||||||||||||||||||
Medical condition: ERCP (Endoscopic Retrograde Cholangiopancreatography) | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001464-30 | Sponsor Protocol Number: 1 | Start Date*: 2006-06-28 |
Sponsor Name:Institut Universitari de Neurorehabiltació Guttmann | ||
Full Title: "Evaluación clínica de los efectos de un agonista colinérgico (Donezepilo) en la rehabilitación de la memoria en pacientes con traumatismo craneoencefálico" | ||
Medical condition: Traumatic Brain Injury (TBI) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006558-17 | Sponsor Protocol Number: | Start Date*: 2010-01-21 |
Sponsor Name:cliniques universitaire de mont godinne | ||
Full Title: | ||
Medical condition: major depression | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003910-33 | Sponsor Protocol Number: -- | Start Date*: 2007-11-19 | |||||||||||
Sponsor Name:OSPEDALE MAGGIORE DI MILANO (IRCCS) | |||||||||||||
Full Title: Randomized controlled study of rituximab and steroid treatment in thyroid-associeted ophthalmopathy (TAO) | |||||||||||||
Medical condition: Thyroid associeted ophthalmopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005583-14 | Sponsor Protocol Number: ART-OFT-RTB-SI-2008 | Start Date*: 2008-09-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: NEW CONSERVATIVE THERAPIES IN RETINOBLASTOMA: DIRECT INTRAARTERIAL (OPHTALMIC ARTERY) CHEMOTHERAPY WITH MELPHALAN FOR INTRAOCULAR RETINOBLASTOMA | |||||||||||||
Medical condition: patients with retinoblastoma | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000983-27 | Sponsor Protocol Number: CLCZ696B2203 | Start Date*: 2012-09-07 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A single-dose, open-label parallel-group study to assess the pharmacokinetics of LCZ696 in subjects with hepatic impairment compared to matched healthy subjects | |||||||||||||
Medical condition: Mild and moderate hepatic impairment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000780-42 | Sponsor Protocol Number: Latanoprost 1/2007 | Start Date*: 2008-02-20 | |||||||||||
Sponsor Name:PH&T SPA | |||||||||||||
Full Title: Evaluation of the therapeutic equivalence of latanoprost PK and Xalatan. Double blind randomized clinical trial in subjects affected by open angle glaucoma or intraocular hypertension. | |||||||||||||
Medical condition: Subjects affected by glaucoma or intraocular hypertension. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004320-36 | Sponsor Protocol Number: DMS/AVASTIN 2006 | Start Date*: 2006-07-25 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: Intravitreal Bevacizumab (Avastin) for neovascular age-related macular degeneration | |||||||||||||
Medical condition: Viasual acuity loss | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001468-34 | Sponsor Protocol Number: HLS01/2008 | Start Date*: 2008-11-20 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA L. SACCO (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: Phase III clinical trial multicenter randomized for the evaluation of the safety and efficacy of the combined treatment of intravitreal triamcinolone and photodynamic therapy versus intravitreal Be... | |||||||||||||
Medical condition: Choroideal neo-vascularization type RAP. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004649-18 | Sponsor Protocol Number: 13001 | Start Date*: 2014-02-21 | |||||||||||
Sponsor Name:Jens Hilligsø | |||||||||||||
Full Title: The effect of phrenic nerve block on postoperative shoulder pain in patients for liver resection – a double blinded randomised controlled trial. | |||||||||||||
Medical condition: Posteoperative shoulder pain following open liver resection surgery . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001502-17 | Sponsor Protocol Number: FARM6FYZB3 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MEYER | |||||||||||||
Full Title: MULTICENTRIC COMPARATIVE RANDOMIZED DOUBLE BLIND CROSS OVER STUDY WITH TACROLIMUS (FK506)0.1% EYEDROPS AND CYCLOSPORINE 1% EYEDROPS IN CHILDREN WITH SEVERE ACTIVE VERNAL KERATOCONJUNCTIVITIS, LASTI... | |||||||||||||
Medical condition: Vernal Keratoconjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001971-36 | Sponsor Protocol Number: RETAANE PED | Start Date*: 2005-05-25 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: PILOT, OPEN NON COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICAY AND SAFETY OF RETAANE (ANECORTAVE ACETATO 15 MG, 0.5 ML DI 30 MG/ML ANECORTAVE ACETATO STERILE SUSPENSION) IN PATIENTS WITH COROID... | |||||||||||||
Medical condition: RETAANE TREATMENT OF COROIDEAL NEOVASCULARIZATION FORMS SECONDARY TO SENILE MACULAR DEGENERATION | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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