NCT00990171

Brief Summary

A prospective long-term follow up of peritoneal dialysis patients' outcome correlates with nutritional status and body composition.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 5, 2009

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 6, 2009

Completed
2.2 years until next milestone

Study Start

First participant enrolled

December 1, 2011

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2016

Completed
Last Updated

April 14, 2014

Status Verified

April 1, 2014

Enrollment Period

5 years

First QC Date

October 5, 2009

Last Update Submit

April 11, 2014

Conditions

Peritoneal DialysisWasting and Malnutrition

Keywords

peritoneal Dialysiswasting and malnutritionnutrition statusbioelectrical impedance analysisbody composition

Outcome Measures

Primary Outcomes (1)

  • Measure BCM could be a nutrition status marker

    5 yrs

Study Arms (1)

PD-BCM

1. Patients at National Taiwan University Hospital (NTUH) 2. Patients who have received PD more than 3 months 3. Patients who sign the informed consents 4. Patients who aged between 20-90 years

Eligibility Criteria

Age20 Years - 90 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

PD patients

You may qualify if:

  • Patients at National Taiwan University Hospital
  • Patients who have received PD more than 3 months
  • Patients who sign the informed consents

You may not qualify if:

  • Patients who have received PD less than 3 months
  • Patients who refuse to sign informed consents
  • Patients who refuse to draw additional blood for research

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

National Taiwan University Hospital

Taipei, Taiwan, 10002, Taiwan

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

plasma dianeal

MeSH Terms

Conditions

CachexiaMalnutrition

Condition Hierarchy (Ancestors)

Weight LossBody Weight ChangesBody WeightSigns and SymptomsPathological Conditions, Signs and SymptomsThinnessNutrition DisordersNutritional and Metabolic Diseases

Central Study Contacts

Jenq-Wen Huang, MD

CONTACT

+886-2-23123456007378@ntuh.gov.tw

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 5, 2009

First Posted

October 6, 2009

Study Start

December 1, 2011

Primary Completion

December 1, 2016

Last Updated

April 14, 2014

Record last verified: 2014-04

Locations

TW(1)