NCT06962124

Brief Summary

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.

Trial Health

35
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 21, 2025

Completed
17 days until next milestone

First Posted

Study publicly available on registry

May 8, 2025

Completed
5 months until next milestone

Study Start

First participant enrolled

October 1, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

May 8, 2025

Status Verified

April 1, 2025

Enrollment Period

Same day

First QC Date

April 21, 2025

Last Update Submit

April 29, 2025

Conditions

Dialysis Related Complication

Outcome Measures

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

    3 month ( 39 session for each patient , 13 session per month)

Study Arms (1)

Effect of measurement of dry weight based on pre dialysis serum sodium measurment on reduction of h

EXPERIMENTAL

measurement of dry weight based on pre dialysis serum sodium

Other: serum sodium measurment

Interventions

serum sodium measurmentOTHER

serum sodium measurment

Effect of measurement of dry weight based on pre dialysis serum sodium measurment on reduction of h

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \- 6- not dependent to mechanical ventilation
  • 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

You may not qualify if:

  • Impaired consciousness 2- participant's withdrawal from the study 5-death 3- severe blood supply problem in the fistula or vascular access 4-migration or travel during the study

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
The effect of accurate measurement of dry weight based on pre dialysis serum sodium measurement on reduction of hemodialysis complicationsAssiut

Study Record Dates

First Submitted

April 21, 2025

First Posted

May 8, 2025

Study Start

October 1, 2025

Primary Completion

October 1, 2025

Study Completion

December 1, 2025

Last Updated

May 8, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share