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Inferior Vena Cava Diameter Guided Fluid Resuscitation versus Conventional Fluid Resuscitation in Patients with Septic Shock

Inferior Vena Cava Diameter Guided Fluid Resuscitation versus Conventional Fluid Resuscitation in Patients with Septic Shock

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202602614037605
Enrollment
68
Registered
2026-02-27
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Circulatory System Cardiology

Interventions

Conventional fluid resuscitation
Inferior Vena Cava Diameter guided fluid resuscitation

Sponsors

Menoufia University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All adult patients (=18 years old) with septic shock (those with persisting hypotension requiring vasopressors to maintain a mean arterial pressure of 65 mm Hg or higher and a serum lactate level greater than 2 mmol/L (18 mg/dL) despite adequate volume resuscitation) who are diagnosed in the first 6 h.

Exclusion criteria

Exclusion criteria: 1) Patients with congestive pulmonary edema or known poor systolic cardiac function (left ventricular ejection fraction = 40%). 2) Patients with known right heart pathology. 3) Patients have or are suspected of having marked ascites, significant bowel dilatation, or conditions that could cause abdominal hypertension. 4) Patients with body mass index = 30 kilograms/meters squared. 5) Patients with concomitant attack of a severe airway disease (eg, asthma or chronic obstructive pulmonary disease that may have confounded the Inferior Vena Cava (IVC) interpretation. 6) Inferior Vena Cava (IVC) could not be identified, or its diameter could not be measured correctly. 7) Patients with end-stage renal disease with or without dialysis. 8) Patients with noninfectious disease as a final diagnosis. 9) Pregnancy. 10) Patients with active hemorrhage. 11) Patients have a living will stating “do not resuscitate”. 12) Patients declined to consent.

Design outcomes

Primary

MeasureTime frame
The 30-day mortality outcome of patients with sepsis-induced tissue hypoperfusion (SITH) and septic shock (SS) who will be treated with Inferior Vena Cava diameter guided fluid management compared with those treated with the conventional strategy.

Secondary

MeasureTime frame
- The six-hour lactate clearance, amount of intravenous (IV) fluid, rate of vasopressor and mechanical ventilator (MV) use. - Change in sequential organ failure assessment (SOFA) score at 72 hours. - Change in Acute Physiology and Chronic Health Evaluation (APACHEII) score. -- Length of stay in ICU.

Countries

Egypt

Contacts

Public ContactWessam Eldin Abd El Rahman Sultan

Faculty of Medicine. Menoufia University

wesamsultan@med.menofia.edu.eg+201010122125

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026