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Effect of intermittent normal saline bolus during hemodialysis on adequacy of dialysis

Effect of intermittent normal saline bolus during hemodialysis on adequacy of dialysis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015100324303N1
Enrollment
50
Registered
2015-11-14
Start date
2015-11-06
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

Hemodialysis. Z49.1

Interventions

Intervention 1: Intervention Group: One Hundred milliliters of normal saline is flushed through the arterial line of extracorporeal tubing three times during the 4-hour period of hemodialysis (once
i.e, receiving 5000 units of unfractionated heparin during hemodialysis. The intervention is for 2 consecutive hemodialysis sessions. Intervention 2: Control Group: The group is dialyzed based on the
Treatment - Other
Intervention Group: One Hundred milliliters of normal saline is flushed through the arterial line of extracorporeal tubing three times during the 4-hour period of hemodialysis (once every hour) in
i.e, receiving 5000 units of unfractionated heparin during hemodialysis. The intervention is for 2 consecutive hemodialysis sessions.
Control Group: The group is dialyzed based on the standard protocol: Five thousands units of unfractionated heparin are given during the 4-hour period of hemodialysis but no intermittent saline flush.

Sponsors

Vice Chancellor for Research and Innovation, Golestan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients with end-stage renal disease treated with maintenance hemodialysis for at least six months; Age above 18 years old; Willingness to participate in the study; On 3 times per week, 4-hours long maintenance hemodialysis; Arteriovenous Fistula or Graft access type; Receives 5000 units of unfractionated heparin during each session of hemodialysis; Hemoglobin concentration 9 to 14 grams per deciliter. Exclusion Criteria: Having acute debilitating disease (cardiovascular, hypertension, cancer and acute infection); Having systolic blood pressure below 90 and above 160 mm Hg.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Adequacy of Hemodialysis (KT/V) and Urea Reduction Ratio (URR). Timepoint: At first and third session of hemodialysis. After a one-week washout time, again at the first and third session of hemodialysis. Method of measurement: Pre and post dialysis serum urea and calculation of URR and KT/V using formula recommended by Ministry of Health and Medical Education.

Secondary

MeasureTime frame
Clot formation in extracorporeal tubing. Timepoint: At the end of each hemodialysis sessions. Method of measurement: By direct observation and grading.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEinollah Mollaei

Golestan University of Medical Sciences

mollaei@goums.ac.ir; einfa15@yahoo.com+98 17 3242 6900

Outcome results

None listed

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