How to Prevent Complications During Dialysis
ConditionDialysis Related Complication
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorAssiut University
About this trial
We aimed to determine the effect of accurate assessment of dry weight based on measuring blood sodium level before dialysis to evaluate the effect of adjustment of ultrafiltration rate on hemodialysis complications and take a step forward to improve patient care and the quality of hemodialysis.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
at least one year history of hemodialysis
adults aged 18 to 65 years old
ability to communicate verbally
with no history of diabetes mellitus, urinary incontinence syndrome, heart and liver failure, and adrenal hypertrophy 5 -no use of antihypertensive and antispasmodic drugs four hours before dialysis
Disqualifiers
None
Trial design
Design model
Single group
Treatments tested in this trial
serum sodium measurment
Other interventionserum sodium measurment
Treatment groups
50 Participants
are divided into 1 treatment groupGroup A: Effect of measurement of dry weight based on pre dialysis serum sodium measurment on reduction of hExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
predict correlation between accurate measurement of dry weight in kilogram by predialytic serum sodium level and incidence of complications.
We aimed to determine the effect of assessment of dry weight based on measuring blood sodium level before dialysis to evaluate the effect of adjustment of ultrafilteration rate on haemodialysis complications and take a step forward to improve patient care and the quality of hemodialysis
Time frame
3 month ( 39 session for each patient , 13 session per month)Locations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: