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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00257504
Other study ID # CBV estimation
Secondary ID
Status Completed
Phase N/A
First received November 21, 2005
Last updated September 11, 2006
Start date November 2005
Est. completion date May 2006

Study information

Verified date September 2006
Source Danish State Hospital
Contact n/a
Is FDA regulated No
Health authority Denmark: National Board of Health
Study type Observational

Clinical Trial Summary

The purpose of the study is to test whether hypotensive episodes during dialysis - caused by withdrawal of fluid drom the circulation - can be predicted by means of two harmless monitoring techniques.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date May 2006
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Chronic hemodialysis patients with central vascular access

Exclusion Criteria:

- Patients below 18 years of age

- Patients unable to give informed consent

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Danish State Hospital Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Danish State Hospital

Country where clinical trial is conducted

Denmark, 

See also
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Completed NCT03504943 - Timing of Intradialytic Exercise and Its Impact on Intradialytic Hypotension N/A
Completed NCT02719223 - The Effect of On-Line Hemodiafiltration Versus High Flux Hemodialysis on Hemodynamic Parameters in Patients With Intra-Dialytic Hypotension N/A
Recruiting NCT04163614 - Blood Pressure Slopes and Ultrafiltration in Hemodialysis Patients N/A
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Completed NCT00657046 - Safety and Benefit Study of Droxidopa to Treat Patients With Intradialytic Hypotension Phase 2