The aim of this study is to conduct an Asia-Pacific, multi-center, prospective observational study to characterize patients with CDI as well as to understand treatment and management of the disease.
Study Type
OBSERVATIONAL
Enrollment
600
Unnamed facility
Kanto Region, Japan
Patient Demographics
Medical history is information which was collected at the CDI diagnosis in this study. The items of the Medical history are indicated below. Concomitant diseases at the CDI diagnosis were included in the Medical history.
Time frame: At the study at the time of CDI diagnosis enrollment
Status at the End of CDI Episode
The patients were observed from the diagnosis to the end of the treatment and got a telephone follow up call after two month from the end of treatment. The categories of the status indicating below are at the end of the treatment, not at the follow up call. Lost to follow-up means the patient number who were lost during the treatment course.
Time frame: From the time of CDI diagnosis to the end of the treatment
Clinical Complication
This study was non-interventional observational study. There were no restriction on the CDI treatment and we did not define to collect AE data. We just defined to collect the data for complications with CDI treatments indicating below. The complications to be checked were defined in the protocol. The information of other complications and AEs were not collected.
Time frame: From the time of CDI diagnosis to recovery or recurrence
Recurrence or Not After 2 Months Follow-up
The patients were observed from the diagnosis to the end of the treatment and got a telephone follow up call after two month from the end of treatment. Unknown includes patient lost, data missing
Time frame: From the time of CDI diagnosis to 2 months follow-up
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