Clinical Trials Directory

Trials / Suspended

SuspendedNCT01132417

In Vitro Activity of Tigecycline Among Key Bacterial Pathogens Exhibiting Multidrug Resistance

Status
Suspended
Phase
Study type
Observational
Enrollment
500 (estimated)
Sponsor
King Faisal University · Academic / Other
Sex
All
Age
Healthy volunteers
Not accepted

Summary

Observational: studies in human beings in which biomedical and/or health outcomes are assessed in pre-defined groups of individuals. Subjects in the study may receive diagnostic, therapeutic, or other interventions, but the investigator does not assign specific interventions to the subjects of the study.

Detailed description

Study Phase Definition: Phase of investigation, as defined by the US FDA for trials involving investigational new drugs. Select only one. N/A: for trials without phases Observational Study Design Case-control: group of individuals with specific characteristics (e.g., conditions or exposures) compared to group(s) with different Time Perspective Cross-sectional: observations or measurements made at a single point in time, usually at subject enrollment Biospecimen Retention - select one Samples Without DNA - samples retained, with no potential for DNA extraction from any retained samples (e.g., fixed tissue, plasma) Biospecimen Description Sputum, whole blood, urine, tissue Enrollment Single group study Number of Groups/Cohorts Definition: Number of study groups/cohorts. Enter 1 for a single-group study. Many observational studies have one group/cohort; case control studies typically have two. One study group, anticipated samples in the rang of 400-500 samples 8. Arms, Groups and Interventions N/L Group/Cohort Label

Conditions

Interventions

TypeNameDescription
DRUGIn Vitro activity of Tigecycline among key bacterial pathogens exhibiting multidrug resistancestudies in human beings in which biomedical and/or health outcomes are assessed in pre-defined groups of individuals. Subjects in the study may receive diagnostic, therapeutic, or other interventions, but the investigator does not assign specific interventions to the subjects of the study.

Timeline

Start date
2009-09-01
Primary completion
2012-06-01
Completion
2012-07-01
First posted
2010-05-28
Last updated
2011-06-23

Locations

1 site across 1 country: Saudi Arabia

Source: ClinicalTrials.gov record NCT01132417. Inclusion in this directory is not an endorsement.