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NCT00939445 Clinical Trial

Short Daily Hemodialysis and Online HDF: Which One is Better?

End Stage Renal Disease Clinical Trial

— SHD  

Official title:
Short Daily Hemodialysis and Online HDF: Which One is Better?

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00939445
Other study ID # VJR-NEPHRO001
Secondary ID
Status Completed
Phase Phase 3
First received July 14, 2009
Last updated December 13, 2015
Start date June 2009
Est. completion date September 2011

Study information
Verified date December 2015
Source Bangkok Metropolitan Administration Medical College and Vajira Hospital
Contact n/a
Is FDA regulated No
Health authority Thailand: Bangkok Metropolitan Administration
Study type Interventional

Clinical Trial Summary

1. To compare the efficacy of

1. Short Daily Hemodialysis

2. Online HDF in term of adequacy of dialysis.

Description:

The investigators intend to compare the efficacy between these modalities of treatment in terms of adequacy and also other parameters such as calcium-phosphorus balance and hematocrit

Recruitment information / eligibility
Status Completed
Enrollment 10
Est. completion date September 2011
Est. primary completion date September 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- stable ESRD

- KT/V > 1.2 for thrice weekly or > 1.8 for twice weekly

Exclusion Criteria:

- Inadequate vascular access flow rate

- Concurrent medical illnesses

- History of non-compliance

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Procedure:
• Online HDF
Online HDF
• Short Daily Hemodialysis
Short Daily Hemodialysis

Locations
Country Name City State
Thailand Renal Unit, BMA Medical College and Vajira Hospital Bangkok

Sponsors (1)
Lead Sponsor Collaborator
Bangkok Metropolitan Administration Medical College and Vajira Hospital

Country where clinical trial is conducted

Thailand, 

Outcome
Type Measure Description Time frame Safety issue
Primary Adequacy 3 months Yes
Secondary Hematocrit, calcium, phosphorus 3 months No
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