Ireland
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Recruiting Observational

Discordance Between Capillary Refill Time and Oxygen Extraction Ratio in Septic Shock

NCT07774962 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-08-17
Last updated
2026-08-19

Condition(s) studied

Septic ShockSepsis

Investigational drug(s) / intervention(s)

Capillary refill time (CRT)Oxygen extraction ratio (O₂ER) assessment

Capillary refill time (CRT): Non-invasive, standardized bedside measurement of capillary refill time on the right index finger.

Oxygen extraction ratio (O₂ER) assessment: Oxygen extraction ratio calculated as (SaO₂ - ScvO₂)/SaO₂ from routinely obtained arterial and central venous blood gases.

Study summary

In septic shock, restoring large-vessel (macrocirculatory) perfusion-reflected by a normal capillary refill time (CRT)-does not always mean that oxygen use at the tissue level has recovered. This mismatch, sometimes called loss of hemodynamic coherence, may be detectable by comparing CRT with the oxygen extraction ratio (O₂ER), a marker of how much oxygen the tissues are extracting from the blood. Patients whose CRT has normalized but whose O₂ER remains abnormal-either too high (suggesting oxygen delivery that is insufficient for demand) or too low (suggesting microcirculatory shunting)-are considered to have a "discordant" perfusion phenotype.

This prospective, single-center, observational cohort study aims to determine how often this CRT-O₂ER discordance occurs at the 6th hour of resuscitation in adult patients with septic shock, and whether it is associated with 28-day mortality. Approximately 100 consecutive adult patients diagnosed with septic shock (with pre-existing central venous and arterial catheters) will be followed. Clinical and laboratory measurements-including CRT, O₂ER, lactate, mottling score, and organ dysfunction scores-will be recorded at hours 0, 6, 12, and 24, with the main phenotype grouping performed at hour 6. The study is purely observational: CRT is a painless, non-invasive bedside measurement, and O₂ER is calculated from blood gas samples already drawn as part of routine care, so no additional interventions or blood draws are performed for research purposes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years * Diagnosis of septic shock according to the Surviving Sepsis Campaign (SSC) 2026 guideline * Presence of both a central venous catheter and an arterial line Exclusion Criteria: * Active bleeding * Ongoing extracorporeal membrane oxygenation (ECMO) * Raynaud phenomenon or significant peripheral vascular disease that makes capillary refill time measurement unreliable (e.g., critical ischemia, amputation, digital ulcer/necrosis, or inability to measure on the right index finger) * Death within the first 6 hours * Inability to obtain hour-6 CRT or blood gas (phenotyping not possible)

Primary outcome measure(s)

  • Prevalence of the discordant CRT-O₂ER phenotype — At hour 6 of resuscitation (6 hours after vasopressor initiation)
    Proportion of patients classified as having a discordant perfusion phenotype (normalized CRT ≤3 s with an abnormal O₂ER, i.e., \>30% or \<20%; combined Group 2a + Group 2b) at hour 6, reported with 95% confidence interval.
  • 28-day all-cause mortality — 28 days from Hour 0 (vasopressor initiation)
    All-cause mortality at 28 days, and its association with the hour-6 perfusion phenotype.

Trial sites (1)

FacilityCityRegionStatus
Basaksehir Cam and Sakura City Hospital Istanbul Turkey (Türkiye) Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07774962 on ClinicalTrials.gov ↗ ← All trials in Turkey