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AQP-1 Polymorphism on Fluid Status in Hemodialysis Patients

the Effect of AQP-1 Polymorphism on Fluid Status of Hemodialysis Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05275387
Enrollment
250
Registered
2022-03-11
Start date
2022-12-01
Completion date
2023-02-28
Last updated
2022-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End Stage Renal Disease on Dialysis

Keywords

AQP1, fluid status

Brief summary

It is a cross sectional observational study. It is to investigate whether AQP-1 polymorphism has any impact on fluid status in hemodialysis patients. The long term stable HD patients in the current center will be enrolled to the study after informed consent. Blood samples will be collected for gene-typing. Fluid status including blood pressure, weekly UF and intra-dialysis body weight change will be collected through their clinical records.

Interventions

observational study, no intervention

Sponsors

RenJi Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* age 18-70 * ESRD * maintained HD * no target weight change during the last week of entering the study and achieve target weight at the end of HD section * informed consented

Exclusion criteria

* expected survival time less than 3 months

Design outcomes

Primary

MeasureTime frameDescription
The total ultrafiltration volume in mls from hemodialysis for the whole week of the recruitmentup to 12 weeksThe ultrafiltration volume of each HD section of the enrollment week will be recorded. The total ultrafiltration volume of the week is the primary outcome measure. (In most cases, HD patients have three HD sections per week.)

Secondary

MeasureTime frameDescription
The total weight gain in kgs of each HD section of the enrollmentup to 12 weeksThe body weight gain of each HD section of the enrollment week will be recorded. The total body weight gain of the week is the secondary outcome measure. (In most cases, HD patients have three HD sections per week.)

Countries

China

Contacts

Primary ContactZanzhe Yu, PhD
yuzzhrsd@163.com15901988349
Backup ContactQi Lu, MD
Luqi@renji.com68383364

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026