- Trials with a EudraCT protocol (435)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (32)
435 result(s) found for: General practice.
Displaying page 1 of 22.
EudraCT Number: 2014-004621-40 | Sponsor Protocol Number: NL50760 | Start Date*: 2015-09-07 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The effect of oral ondansetron on referral rate in children aged 6 months to 6 years attending in primary care out of hours service with acute gastro-enteritis and vomiting. | ||
Medical condition: Gastroenteritis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003582-25 | Sponsor Protocol Number: NL59128 | Start Date*: 2017-01-23 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: The added effect of oral ondansetron to care-as-usual on persisting vomiting in children aged 6 months to 6 years, presenting at primary care out of hours service with acute gastro-enteritis and co... | ||
Medical condition: Gastroenteritis | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000574-69 | Sponsor Protocol Number: D9612L00076 | Start Date*: 2006-04-07 |
Sponsor Name:AstraZeneca A/S | ||
Full Title: Development of an algorithm for identification of responders to short term treatment with esomeprazol (Nexium) in primary care. | ||
Medical condition: acid related disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-001591-11 | Sponsor Protocol Number: 3.4.11.049 | Start Date*: 2012-12-21 |
Sponsor Name:Erasmus MC | ||
Full Title: Symptomatic treatment of pollen related allergic rhinoconjunctivitis and the relation with asthma with children in the General practice | ||
Medical condition: Allergic Rhinitis Asthma | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002214-13 | Sponsor Protocol Number: IIBSP-OXI-2013-62 | Start Date*: 2013-10-28 |
Sponsor Name:Institut de Recerca de l?Hospital de la Santa Creu i Sant Pau ? IIB Sant Pau | ||
Full Title: Evaluation of oxidative stress associated with the administration of two different concentrations of oxygen for the maintenance of general anesthesia | ||
Medical condition: General anesthesia and oxidative stress | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004114-28 | Sponsor Protocol Number: 0801-38 | Start Date*: 2009-04-01 | |||||||||||
Sponsor Name:Erasmus Medical Center; Department of general practice [...] | |||||||||||||
Full Title: Effectiveness of Diclofenac versus Paracetamol in primary care patients with knee osteoarthritis. | |||||||||||||
Medical condition: Knee Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001567-37 | Sponsor Protocol Number: KUKIDEX-2 | Start Date*: 2016-11-24 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Efficacy of single dose intranasal dexmedetomidine for conscious sedation in dental practice in dentophobic uncooperative patients with intellectual disability. | ||
Medical condition: dentophobia intellectual disability | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002323-28 | Sponsor Protocol Number: prop01 | Start Date*: 2016-06-28 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Blood concentration and pharmacokinetic analysis of propofol following administration of single induction dose in small children | ||
Medical condition: Children scheduled for elective surgery | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000477-21 | Sponsor Protocol Number: 01579 | Start Date*: 2017-03-27 | |||||||||||
Sponsor Name:Georg-August-Universität Göttingen, Stiftung Öffentlichen Rechts, Universitätsmedizin Göttingen | |||||||||||||
Full Title: Reducing antibiotic use for uncomplicated urinary tract infection in gen-eral practice by treatment with Uva ursi - a comparative effectiveness trial | |||||||||||||
Medical condition: uncomplicated urinary tract infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000961-22 | Sponsor Protocol Number: 16/009U | Start Date*: 2016-11-14 |
Sponsor Name:Ziekenhuis Oost-Limburg | ||
Full Title: Quality of analgesia after ultrasound-guided specific blocks of the distal tibial and deep peroneal nerves with 15 mL of a 50:50 mixture bupivacaine 0.5% and liposome bupivacaine (Exparel®) )1.3% ... | ||
Medical condition: Hallux valgus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000864-28 | Sponsor Protocol Number: DAP-PEDOST-11-03 | Start Date*: 2014-01-02 | |||||||||||||||||||||
Sponsor Name:Cubist Pharmaceuticals, LLC | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blinded Comparative Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Daptomycin Versus Active Comparator in Pediatric Subjects With Acute Hematogeno... | |||||||||||||||||||||||
Medical condition: Acute Hematogenous Osteomyelitis Due to Gram-Positive Organisms | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) HU (Completed) IT (Completed) ES (Completed) GR (Completed) LV (Completed) GB (Completed) EE (Completed) BG (Completed) FR (Completed) SI (Completed) Outside EU/EEA | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012210-48 | Sponsor Protocol Number: 20407 | Start Date*: 2009-08-06 | ||||||||||||||||
Sponsor Name:Leiden University Medical Centre | ||||||||||||||||||
Full Title: Monochloroacetic acid versus cryotherapy in the treatment of warts: A Randomised Clinical Trial (WARTS-2) | ||||||||||||||||||
Medical condition: All patients from the age of 4 onward, who present themselves to their practice with one or more new warts of the type vulgaris on hands or feet. | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002660-13 | Sponsor Protocol Number: FEHD | Start Date*: 2016-11-21 |
Sponsor Name:Consorcio Hospital General Universitario de Valencia | ||
Full Title: Treatment of Ferropenic Anaemia due to acute gastrointestinal bleeding: oral vs intravenous iron therapy | ||
Medical condition: FERROPENIC ANAEMIA DUE TO ACUTE GASTROINTESTINAL BLEEDING | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000381-11 | Sponsor Protocol Number: NL42823.018.13 | Start Date*: 2013-05-17 | ||||||||||||||||||||||||||
Sponsor Name:Academisch Medisch Centrum | ||||||||||||||||||||||||||||
Full Title: Paracetamol or NSAID's in acute musculoskeletal syndromes | ||||||||||||||||||||||||||||
Medical condition: acute musculoskeletal syndromes | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019513-24 | Sponsor Protocol Number: 10_022 | Start Date*: 2011-03-03 |
Sponsor Name:London School of Hygiene & Tropical Medicine | ||
Full Title: Antibiotics for exacerbations of chronic obstructive pulmonary disease: a pilot randomised trial within the General Practice Research Database | ||
Medical condition: Diagnosed at a GP visit as suffering from acute exacerbation of COPD a. Medical history of COPD b. Increase in dyspnoea AND increase of (non-purulent) sputum volume | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-014913-28 | Sponsor Protocol Number: 09_056R | Start Date*: 2011-02-03 |
Sponsor Name:London School of Hygiene & Tropical Medicine | ||
Full Title: RETRO-PRO: The effectiveness of simvastatin compared to atorvastatin: an e-clinical randomised trial within a research database in routine clinical practice - a feasibility study | ||
Medical condition: subjects who in the opinion of the GP investigator would require a statin for primary prevention according to the 2008 NICE guideline on lipid modification: adults over 40 who have a 20% or greater... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004160-22 | Sponsor Protocol Number: LUMC_IEMO80PLUS_1.0 | Start Date*: 2013-06-18 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: IEMO 80-plus thyroid trial | ||
Medical condition: Subclinical hypothyroidism | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003766-27 | Sponsor Protocol Number: 848015011 | Start Date*: 2018-07-18 | |||||||||||
Sponsor Name:VU University Medical Centre | |||||||||||||
Full Title: The DREAMING study: Efficacy of low dose amitriptyline and mirtazapine for insomnia disorder: a double-blind, randomized, placebo-controlled trial in general practice | |||||||||||||
Medical condition: Insonnia disorder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000834-36 | Sponsor Protocol Number: 43806 | Start Date*: 2013-09-26 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Simvastatin addition to improve symptoms, cognition and metabolic syndrome in patients with recent-onset schizophrenia. | ||
Medical condition: Schizophrenia, schizoaffective or schizophreniform disorder (DSM-IV 295.*) or psychosis NOS (not otherwise specified) (298.9) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-002474-30 | Sponsor Protocol Number: 2019-002474-30 | Start Date*: 2019-12-20 | |||||||||||
Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
Full Title: PERSONALIZED MOLECULAR DRIVEN SURGERY ACCORDING TO BRCA MUTATIONAL STATUS IN ADVANCED EPITHELIAL OVARIAN CANCER PATIENTS WITH HIGH TUMOR LOAD | |||||||||||||
Medical condition: ADVANCED OVARIAN CARCINOMA | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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