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                   89 records for 55 trials found!
Trials are sometimes recorded in more than one registry. These records can refer to each other using the 'Secondary ID' field. The search portal uses these Secondary IDs to group records about the same trial together in the search results.
Each group of records referring to a trial is displayed in table that is seen by pressing the + symbol. The record with the earliest date of registration is always shown first.
 
 
 
 
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Recruitment statusMain ID Public TitleDate of Registration
Not recruitingNCT02486237
Complications in Central American Diabetic Patients: Historic Cohort
22/06/2015
Not AvailableEUCTR2015-001540-10-Outside-EU/EEA
A phase III study to assess the efficacy, immunogenicity and safety of GSK Biologicals’ human rotavirus (HRV) vaccine given concomitantly with routine expanded program on immunisation (EPI) vaccinations including oral poliovirus vaccine (OPV) in healthy infants across 6 countries in Latin America.
11/06/2015
Not AvailableEUCTR2013-003155-38-Outside-EU/EEA
Study to evaluate immunogenicity and safety of GlaxoSmithKline (GSK) Biologicals’ quadrivalent influenza vaccine GSK2282512A when administered to children 6 to 35 months of age
27/05/2015
Not AvailableEUCTR2015-001514-97-Outside-EU/EEA
Study to evaluate the efficacy of GSK Biologicals’ quadrivalent influenza vaccine, GSK2282512A, (FLU Q-QIV) when administered in children 3 to 8 years of age
27/05/2015
RecruitingRBR-6gphkr
CQAB149BAR01 - 24-week study to assess which treatment is safer and bring more benefits to patients with COPD (Chronic Obstructive Pulmonary Disease) combination budesonide / indacaterol vs fluticasone / salmeterol
04/03/2015
RecruitingNCT02307201
Magnesium Sulfate During the Postpartum in Women With Severe Preeclampsia
24/11/2014
RecruitingNCT02466867
An Open Label Pharmacokinetic Study of Naftin for Tinea Corporis
29/10/2014
RecruitingNCT02227290
Pediatric Subjects With Tinea Corporis
25/08/2014
AuthorisedEUCTR2012-002862-11-EE
Assessment of the Safety Profile and Efficacy of Ceftolozane/Tazobactam
Recruitment statusMain IDPublic titleDate of registration
AuthorisedEUCTR2012-002862-11-HUNA07/10/2014
AuthorisedEUCTR2012-002862-11-BE-11/08/2014
AuthorisedEUCTR2012-002862-11-CZAssessment of the Safety Profile and Efficacy of Ceftolozane/Tazobactam09/09/2014
AuthorisedEUCTR2012-002862-11-SKAssessment of the Safety Profile and Efficacy of Ceftolozane/Tazobactam13/10/2014
AuthorisedEUCTR2012-002862-11-LVAssessment of the Safety Profile and Efficacy of Ceftolozane/Tazobactam in Nosocomial Pneumonia26/08/2014
AuthorisedEUCTR2012-002862-11-AT-08/01/2015
06/08/2014
AuthorisedEUCTR2013-001231-51-IT
Efficacy and Immunogenicity Study of Quadrivalent Influenza Vaccine Administered via the Intramuscular Route in Healthy Children Aged 6 to 35 Months 13/03/2014
    
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Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
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