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Comparison the effect of High Flux with Low Flux membrane in Patient's Comfort, Level of Electrolytes and Clearances of Articles in Hemodialysis' Patients

Comparison the effect of High Flux with Low Flux membrane in Patient's Comfort, Level of Electrolytes and Clearances of Articles in Hemodialysis' Patients

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201106094505N3
Enrollment
30
Registered
2011-07-10
Start date
2011-06-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

End stage renal disease. End-stage renal disease

Interventions

Intervention 1: Selected patients in a Phase ,2 session of dialysis with low-flow filter, is performed. During the second session, a blood sample to check the values of variables before and after hemo
Treatment - Other
Selected patients in a Phase ,2 session of dialysis with low-flow filter, is performed. During the second session, a blood sample to check the values of variables before and after hemodialysis is done
In other step,the same Selected patients, 2 session of dialysis with High-flow filter, is performed. During the second session, a blood sample to check the values of variables before and after hemodia

Sponsors

Vice chancellor for research and tecnology Hamedan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: An arteriovenous fistula or graft; three dialysis sessions weekly; Dialysis four hours per session; tolerate dialysis sessions; History of dialysis for at least six months; Full alertness and ability to project participation; Hello not for dialysis patients; Dialysis performed by the machine fixed; No history of heart disease; acute pulmonary disease; Having less than three liters of ultrafiltration; hemoglobin more than 8 mg per dL; Non-antibiotic drugs to be false values ??for creatinine such as Trimetoprim Exclusion criteria: severe hypotension; severe complications of hemodialysis; lack of patient cooperation; patient discontinuation Dialysis and allergic reactions can be excluded.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Systolic and diastolic blood pressure. Timepoint: per a hours. Method of measurement: sphygmomanometer.;Clearance Na,K,P,BUN,Cr. Timepoint: before and after hemodialysis. Method of measurement: Using Electrolyte Machine.

Secondary

MeasureTime frame
Itch. Timepoint: during and 48 hours after hemodyalisis. Method of measurement: VAS.;Nauseas. Timepoint: during and 48 hours after hemodialysis. Method of measurement: VAS measure.;Vomiting. Timepoint: during and 48 hours after hemodialysis. Method of measurement: Four state criteria.;Headache. Timepoint: Four state criteria. Method of measurement: VAS neasure.;Muscle pain. Timepoint: during and 48 hours after hemodialysis. Method of measurement: VAS measure.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasool Kavyannejad

Hamadan University of Medical Sciences & Health Services

rasol.kavian@umsha.ac.ir+98 81 1827 6296

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026