- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Abdominal guarding.
Displaying page 1 of 1.
EudraCT Number: 2005-000448-99 | Sponsor Protocol Number: 3074A1-315-WW | Start Date*: 2005-12-12 |
Sponsor Name:Wyeth Pharmaceuticals, Inc., Global Medical Affairs | ||
Full Title: A Multicenter, Open-Label, Randomized Comparative Study of Tigecycline vs Ceftriaxone Sodium Plus Metronidazole for the Treatment of Hospitalized Subjects With Complicated Intra-abdominal Infection. | ||
Medical condition: Complicated Intra-Abdominal Infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) GB (Completed) ES (Completed) FI (Completed) DK (Completed) GR (Completed) PT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-015578-37 | Sponsor Protocol Number: BAY12-8039/11643 | Start Date*: 2010-05-10 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A randomized, double-blind, multicenter trial to evaluate the safety and efficacy of sequential (intravenous, oral) moxifloxacin versus comparator in pediatric subjects with complicated intraabdomi... | |||||||||||||
Medical condition: Complicated intra-abdominal infections (cIAI) | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) ES (Prematurely Ended) LV (Completed) LT (Completed) CZ (Completed) BE (Prematurely Ended) HU (Completed) BG (Completed) GR (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000874-56 | Sponsor Protocol Number: BAY12-8039/11976 | Start Date*: 2006-06-12 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A prospective, randomized, double dummy, double blind, multi-center trial comparing the safety and efficacy of moxifloxacin 400 mg IV QD 24 hours to that of ertapenem 1.0 g IV QD 24 hours for 5 to ... | |||||||||||||
Medical condition: Complicated intra-abdominal Infections | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Completed) BE (Completed) EE (Completed) DE (Completed) ES (Completed) LV (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004495-12 | Sponsor Protocol Number: KCA2011/APAC | Start Date*: 2017-05-18 |
Sponsor Name:VU University Medical center | ||
Full Title: Antibiotic treatment alone for children with acute appendicitis; a prospective cohort study part of the Antibiotic versus Primary Appendectomy for Children with acute appendicitis; the APAC trial. | ||
Medical condition: Radiologically confirmed simple appendicitis, defined as: a. Clinical findings: Unwell, but not generally ill, Localized tenderness in the right iliac fossa region, Normal/hyperactive bowel sound... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001747-69 | Sponsor Protocol Number: GEMII-1 | Start Date*: 2011-10-28 | |||||||||||
Sponsor Name:Monash University [...] | |||||||||||||
Full Title: Combination gefitinib and methotrexate to treat ectopic pregnancies II | |||||||||||||
Medical condition: Ectopic pregnancy or pregnancy of unknown location. | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003052-70 | Sponsor Protocol Number: APAC2016 | Start Date*: 2016-11-10 | |||||||||||
Sponsor Name:Academic Medical Center of Amsterdam | |||||||||||||
Full Title: Initial non-operative treatment strategy versus appendectomy treatment strategy for simple appendicitis in children aged 7-17 years old. APAC study | |||||||||||||
Medical condition: Acute uncomplicated (simple) appendicitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
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