Body-fluid Balance and Drinking Habits in Patients With Retinal Vascular Occlusion

This study is currently recruiting participants.
Verified September 2013 by Technische Universität Dresden
Sponsor:
Information provided by (Responsible Party):
Dr. med. Evelyn Voigt, Dresden University of Technology
ClinicalTrials.gov Identifier:
NCT01939119
First received: September 3, 2013
Last updated: September 5, 2013
Last verified: September 2013
  Purpose

The purpose of this study is to examine the body-fluid balance in patients with retinal vascular occlusion and the influence of drinking habits and hemodilution on the degree of body hydration.


Condition
Dehydration
Retinal Vascular Occlusion

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Examination of the Body-fluid Balance in Patients With Retinal Vascular Occlusion Before and During Hemodilution and the Influence of Drinking Habits on the Degree of Body Hydration

Resource links provided by NLM:


Further study details as provided by Technische Universität Dresden:

Primary Outcome Measures:
  • changes in body-fluid balance [ Time Frame: 1 week ] [ Designated as safety issue: No ]
    The influence of hemodilution on body-fluid balance in patients with retinal vascular occlusion is examined


Secondary Outcome Measures:
  • number of participants with dehydration [ Time Frame: 1 week ] [ Designated as safety issue: No ]
    All patients are asked to fill in a questionnaire concerning their drinking habits (thirst, fluid intake). Patients body-fluid balance during hemodilution is measured with bioimpedance spectroscopy (Body Composition Monitor, Fresenius)


Estimated Enrollment: 30
Study Start Date: January 2013
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: October 2013 (Final data collection date for primary outcome measure)
Groups/Cohorts
retinal vascular occlusion
Patients with retinal vascular occlusion undergo a hematocrit dependent 5 day hemodilution

Detailed Description:

Patients with retinal vascular occlusion who are hospitalized for hemodilution and cardiovascular risk assessment are asked to report their drinking habits. Hydration status before and during hemodilution is assessed with a body-fluid analyzing scale.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

patients with retinal vascular occlusion

Criteria

Inclusion Criteria:

  • informed consent
  • age over 18 years

Exclusion Criteria:

  • age under 18 years
  • hypertensive urgency
  • myocardial infarction < 4 weeks ago, chest pain
  • heart rhythm disorders, high degree valvular defects
  • pacemaker, defibrillator
  • peripheral arterial occlusive disease
  • end stage renal disease
  • acute hepatitis, chronic inflammatory intestinal disease
  • pregnancy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01939119

Contacts
Contact: Evelyn Voigt, MD 00493514583381 evelyn.voigt@uniklinikum-dresden.de
Contact: Karin Pillunat, MD 00493514583274 karin.pillunat@uniklinikum-dresden.de

Locations
Germany
University Eye Clinic Recruiting
Dresden, Germany/ Saxony, Germany, 01307
Sponsors and Collaborators
Technische Universität Dresden
Investigators
Study Director: Lutz E Pillunat, MD University Eye Clinic Dresden
  More Information

No publications provided

Responsible Party: Dr. med. Evelyn Voigt, Dr. med., Dresden University of Technology
ClinicalTrials.gov Identifier: NCT01939119     History of Changes
Other Study ID Numbers: VascOcclusion/Drinking2013
Study First Received: September 3, 2013
Last Updated: September 5, 2013
Health Authority: Germany: Ministry of Health

Keywords provided by Technische Universität Dresden:
retinal vascular occlusion
drinking habits
body hydration
body-fluid balance

Additional relevant MeSH terms:
Dehydration
Water-Electrolyte Imbalance
Metabolic Diseases
Pathologic Processes

ClinicalTrials.gov processed this record on April 17, 2014