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Initial filling of 0.9% Sodium Chloride versus 20% Albumin in preventing blood pressure drop in patients with Acute Renal Failure during hemodialysis: a comparative clinical study

Initial priming of 0.9% Sodium Chloride vs 20% Albumin in preventing hemodynamic instability in patients with Acute Kidney Injury during hemodialysis: a randomized clinical trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
REBEC
Registry ID
RBR-9m634y8
Enrollment
Unknown
Registered
2025-04-24
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Acute Kidney Injury

Interventions

This is a prospective randomized clinical trial that will evaluate the prevention of hemodynamic instability during prolonged hemodialysis sessions in patients with acute kidney injury associated with
E02.319.267

Sponsors

Hospital das Clínicas da Faculdade de Medicina de Botucatu da Universidade Estadual Paulista
Lead Sponsor
Hospital das Clínicas da Faculdade de Medicina de Botucatu da Universidade Estadual Paulista
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Men and women; over 18 years old; with acute kidney injury; admitted to the intensive care unit using norepinephrine at a dose of 0.3 to 0.6 ucg/kg/min; and undergoing prolonged hemodialysis for at least 3 sessions

Exclusion criteria

Exclusion criteria: Patients under 18 years of age; and treated with less than two sessions of prolonged hemodialysis

Design outcomes

Primary

MeasureTime frame
Improvement in metabolic control is expected after 3 sessions of prolonged hemodialysis (urea, creatinine, potassium and bicarbonate levels), assessed through blood collection. Improvement in volume control is expected after 3 sessions of prolonged hemodialysis assessed through cumulative fluid balance. To assess the recovery of renal function through laboratory tests collected at the beginning and end of the study

Secondary

MeasureTime frame
has no secondary outcome

Countries

Brazil

Contacts

Public ContactSimone Ferreira

Hospital das Clínicas da Faculdade de Medicina de Botucatu da Universidade Estadual Paulista

enfermeirasi2007@yahoo.com.br+55(014)996051969

Outcome results

None listed

Source: REBEC (via WHO ICTRP)