- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03417791
Recovery of Serum Creatinine at Discharge Impacts Mortality (RECOST)
January 24, 2018 updated by: Guangdong Provincial People's Hospital
Recovery of Serum Creatinine at Discharge Impacts Mortality, Long-term and Short-term
The aim of our study is to assess the mortality in the in-hospital patients who have elevated serum creatinine.
A registry of patients with increased serum creatinine during hospital was conducted at the Guangdong General Hospital from January 1st, 2007 to December 30th, 2013.
The primary clinical outcome is all-cause mortality, followed from the date of hospital discharge to Dec 30th 2018.
Patients were divided into three groups, according to the serum creatinine recovery ratio (discharge/max serum creatinine).
All-cause mortality, including the date of death, was identified from the electronic hospitalization data, phone follow-up, and confirmed by the household registration (HUKOU) system, a record of registration required by law in China.
Baseline characteristics, including primary disease diagnosis, blood pressure, major treatment, drug use and et al, were collected.
Demographic data were collected from the electronic hospitalization data and electronic hospital discharge records.
All co-morbid conditions were identified using International Statistical Classification of Diseases, Tenth Revision (ICD-10), coding algorithms applied to electronic physician claims and electronic hospital discharge records.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
20000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510080
- Guangdong General Hospital
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
the registry and follow up of consecutive patients with increased serum creatinine during hospital in 2007
Description
Inclusion Criteria:
- In-hospital patients in Guangdong General Hospital in 2007
- Age>=18y
- Patients with increased serum creatinine during hospital
Exclusion Criteria:
- Death during hospital
- Diagnosed with End-stage renal disease
- given the renal replace therapy during hospital
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
kidney function recovery
the registry and follow up of consecutive patients with increased serum creatinine during hospital in 2007
|
no intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
all-cause mortality
Time Frame: 10 years
|
all-cause mortality
|
10 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Liming Yao, M.D., Guangdong Provincial People's 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)
January 1, 2007
Primary Completion (Anticipated)
December 30, 2018
Study Completion (Anticipated)
December 30, 2018
Study Registration Dates
First Submitted
January 17, 2018
First Submitted That Met QC Criteria
January 24, 2018
First Posted (Actual)
January 31, 2018
Study Record Updates
Last Update Posted (Actual)
January 31, 2018
Last Update Submitted That Met QC Criteria
January 24, 2018
Last Verified
November 1, 2017
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- GDREC2017296H
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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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