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Comparison of fluid therapy methods in patients with sepsis: A clinical trial in the intensive care unit of Al-Zahra Hospital

Comparison of two methods of routine fluid therapy and targeted fluid therapy based on peripheral perfusion index in patients with sepsis hospitalized in the intensive care unit of Al-Zahra Hospital: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240804062637N1
Enrollment
60
Registered
2024-08-16
Start date
2024-08-22
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Sepsis. Other sepsis

Interventions

Intervention 1: Control group: Control group: All selected patients will be treated for sepsis based on standard guideline recommendations. According to these guidelines, 30 mL/kg of lactated Ringer's

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with sepsis hospitalized in the intensive care unit

Exclusion criteria

Exclusion criteria: Inaccessible peripheral perfusion

Design outcomes

Primary

MeasureTime frame
Prevalence of peripheral hypoperfusion among the study groups. Timepoint: Every 30 seconds for 5 minutes daily over a span of seven days. Method of measurement: Pulse oximeter.

Secondary

MeasureTime frame
Blood lactate level. Timepoint: Between 6 and 24 hours after sepsis diagnosis. Method of measurement: Blood sample.;Mean arterial pressure. Timepoint: Between 6 and 24 hours after sepsis diagnosis. Method of measurement: Intensive care monitoring device.;Serum cystatin C level. Timepoint: Between 6 and 24 hours after sepsis diagnosis. Method of measurement: Blood sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSara Mousavi

Esfahan University of Medical Sciences

s.mousavi@pharm.mui.ac.ir+98 31 3792 7072

Outcome results

None listed

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