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Comparison between saline flush technique and saline free technique in preventing clotting of dialysis circuit: A randomised controlled trial

Comparison between intermittent saline flush technique and saline free technique in preventing clotting of extracorporeal circuit in heparin free hemodialysis: A randomised controlled trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/06/034441
Enrollment
110
Registered
2021-06-29
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: N19- Unspecified kidney failure

Interventions

Intervention1: Not giving saline flush: In no-saline or saline-free arm, hemodialysis will be conducted without intermittent saline flushes Control Intervention1: Intermittent saline flush strategy: I

Sponsors

Department of Nephrology PostGraduate Institute Of Medical Education and Research Chandigarh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with renal dysfunction due to any etiology who have been prescribed heparin-free hemodialysis from a nephrologist will be considered eligible for this study if they are above 18 years of age and satisfy ANY of the following criteria 1) Patients suffering from thrombocytopenia (Platelet 2) Patients with coagulopathy with either INR > 2 or aPTT > 40 seconds. 3) Patients with evidence of acute or active bleeding from any site. 4) Patients suffering from any bleeding diathesis. 5) Patients receiving any form of systemic anticoagulation in therapeutic doses.

Exclusion criteria

Exclusion criteria: Patients who meet ANY of the following criteria will be excluded: 1)Patients unable to attain and tolerate hemodialysis at blood flow >= 250ml/min. 2)Patient planned to receive blood products during hemodialysis. 3)Patients suffering from a known thrombophilic state. 4)Patient unwilling to give written informed consent to participate in the study.

Design outcomes

Primary

MeasureTime frame
Clotting of extracorporeal circuit more than or equal to grade 3 clottingTimepoint: Within 4 hours of dialysis

Secondary

MeasureTime frame
Fraction of dialyzerâ??s fibre bundle volume lossTimepoint: Within 4 hours of dialysis

Countries

India

Contacts

Public ContactDr Shubham Shukla

Postgraduate Institute of Medical Education and Research

shubham9222@gmail.com9915350586

Outcome results

None listed

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