NCT03471299

Brief Summary

This study assesses retrospectively the association of mortality on UFR assessments in our study population undergoing HD.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
759

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Apr 2017

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

April 1, 2017

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2018

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2018

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

March 13, 2018

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 20, 2018

Completed
Last Updated

March 20, 2018

Status Verified

March 1, 2018

Enrollment Period

10 months

First QC Date

March 13, 2018

Last Update Submit

March 13, 2018

Conditions

Hemodialysis

Keywords

Ultrafiltration rate

Outcome Measures

Primary Outcomes (1)

  • Ultrafiltration rate (ml/hr/kg)

    7 years

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

In this study, 759 patients who had undergone maintenance HD for \>1 year at Tojinkai Hospital, kyoto, Japan. The present study examined data from all individual with regular thrice weekly maintenance HD treatment.

You may qualify if:

  • Patients with stable undergoing hemodialysis for \>1 year.

You may not qualify if:

  • Patients with combined therapy with peritoneal dialysis and HD. Patients without records of laboratory investigations during this period. Patients with transferred hospital and those lost to follow-up.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Graduate School of Applied Informatics, University of Hyogo

Kobe, Hyōgo, 650-0047, Japan

Location

Study Officials

  • Yuko Mizuno-Matsumoto, Ph.D

    Graduate School of Applied Informatics, University of Hyogo

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
clinical engineer

Study Record Dates

First Submitted

March 13, 2018

First Posted

March 20, 2018

Study Start

April 1, 2017

Primary Completion

February 1, 2018

Study Completion

March 1, 2018

Last Updated

March 20, 2018

Record last verified: 2018-03

Locations

JP(1)