- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01195519
The Assessment of Quality of Life in Patients With Peritoneal Dialysis and Hemodialysis
April 22, 2011 updated by: Taipei Medical University WanFang Hospital
The Study Will Investigate the Quality of Life in PD or HD Patients
Currently, lots of researches aimed at quality of life of patients with peritoneal dialysis and hemodialysis related issues.
There is no study related to establish the predictive model of quality of life.
This study will investigate the predictive model of quality of life in terms of peritoneal dialysis (PD) or hemodialysis (HD) patients.
These results will offer the further evidence to the government to develop the effective interventions for dialysis patients.
The optimal goal is to promote the quality care.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
95
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: Wan Fang, hospital
- Phone Number: 8117 02-29307930
- Email: huiyi072@yahoo.com.tw
Study Locations
-
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NO.111, Section 3, Hsing-Long Rd, Taipei
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Taipei, NO.111, Section 3, Hsing-Long Rd, Taipei, Taiwan
- Recruiting
- Taipei Medical University WanFang Hospital
-
Contact:
- Tso-Hsiao Chen, Dean
- Phone Number: 8117 02-29307930
- Email: tsohsiao@tmu.edu.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 to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
peritoneal dialysis and hemodialysis patients
Description
Inclusion Criteria:
- above 20 years old PD or HD patients
- conscious clear and no psychosis
- literate and can communicate
- willing to participate and sign informed consent
Exclusion Criteria:
- Not volunteer
- subject felt weak or uncomfortable and patients decision to withdraw from the study
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
Cohorts and Interventions
Group / Cohort |
---|
peritoneal dialysis and hemodialysis patients
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Tso-Hsiao Chen, Taipei Medical University WanFang Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
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
September 1, 2010
Study Completion (ANTICIPATED)
September 1, 2011
Study Registration Dates
First Submitted
September 3, 2010
First Submitted That Met QC Criteria
September 3, 2010
First Posted (ESTIMATE)
September 6, 2010
Study Record Updates
Last Update Posted (ESTIMATE)
April 26, 2011
Last Update Submitted That Met QC Criteria
April 22, 2011
Last Verified
April 1, 2011
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 99039
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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