- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04061889
Clinical Epidemiology Cohort Study for Patient Living With HIV
August 17, 2019 updated by: Hung Chin Tsai, Kaohsiung Veterans General Hospital.
This is a retrospective observational cohort study for the patient living with HIV aiming to understand more in disease progress, resistant mutation, comorbidity, and common coinfection.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
2000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hung Chin Tsai, MD, PhD
- Phone Number: +886-7-3468299
- Email: hctsai1011@yahoo.com.tw
Study Contact Backup
- Name: Che Chan Chou
- Phone Number: +886-7-3468299
Study Locations
-
-
Kaohsiung City
-
Kaohsiung, Kaohsiung City, Taiwan
- Recruiting
- Kaohsiung veteran general hospital
-
Contact:
- Hung Chin Tsai, MD, PhD
- Phone Number: +886-7-3468299
- Email: hctsai1011@yahoo.com.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
HIV-1 infected adult
Description
Inclusion Criteria:
- Patient living with HIV receiving follow-up in Kaohsiung VGH
Exclusion Criteria:
- not applicable
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Hazard ratio of cohort epidemiology characteristics in treatment failure, renal failure and hepatitis D coinfection
Time Frame: on average of 3 year
|
on average of 3 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Hung Chin Tsai, MD,PhD, Kaohsiung veteran general hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2019
Primary Completion (Anticipated)
March 31, 2022
Study Completion (Anticipated)
March 31, 2022
Study Registration Dates
First Submitted
August 15, 2019
First Submitted That Met QC Criteria
August 17, 2019
First Posted (Actual)
August 20, 2019
Study Record Updates
Last Update Posted (Actual)
August 20, 2019
Last Update Submitted That Met QC Criteria
August 17, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- VGHKS19-CT4-02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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