Skip to content

A STUDY TO ASSESS TWO DIFFERENT TECHNOLOGIES OF THERAPEUTIC PLASMA EXCHANGE MODALITY IN KIDNEY DISEASES

COMPARISON OF TWO DIFFERENT TECHNOLOGIES FOR PLASMA EXCHANGE - CENTRIFUGAL VERSUS MEMBRANE IN KIDNEY DISEASE.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/043871
Enrollment
20
Registered
2022-07-08
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: N29- Other disorders of kidney and ureter in diseases classified elsewhere

Interventions

Intervention1: Therapeutic plasma exchange by Centrifugal Technology: Therapeutic plasma exchange done by Centrifugal technology, patients allocated randomly in this arm total 10 cases to be allocated

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.No evidence of active infection 2.Willing to give informed consent for the procedure (In patients who are incompetent to consent, consent shall be taken from the surrogate) 3.Those who not enrolled in any other study

Exclusion criteria

Exclusion criteria: 1.Pregnancy 2.Microbiological or radiological evidence of active infection 3.Known allergy to Plasma, Protamine or Heparin. 4.Severe systemic illness like HIV 5.Patients with vasculitis due to secondary causes (diagnosis of a different rheumatic disease, Hepatitis B, Hepatitis C, HIV infection) 6.Mechanically ventilated patients 7.Renal or any other transplant recepients would be excluded.

Design outcomes

Primary

MeasureTime frame
a.Compare the centrifugal and membrane filtration technologies for TPE in renal disease patients in terms of their efficacy in plasma removal. b.Compare the Post exchange clinical, biochemical, and hematological profile in the two groups c.Calculation of the TPE procedure costs in the two modalities Timepoint: recruitment 12 months results and analysis 2months

Secondary

MeasureTime frame
Patient Outcome- Adverse events and Morbidity and mortality at 30 days and 90 days TPE cycle completionTimepoint: at 30 and 90 days post TPE cycle completion

Countries

India

Contacts

Public ContactDr Divjot Singh Lamba

PGIMER, Chandigarh.

div834@gmail.com9815464100

Outcome results

None listed

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