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The Effect of Remote Ischemic Conditioning on the Microcirculation in Sepsis

Effects of Remote Ischemic Conditioning on Microcirculatory Alterations in Patients With Sepsis

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04644926
Enrollment
26
Registered
2020-11-25
Start date
2018-02-01
Completion date
2020-09-01
Last updated
2021-03-03

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

Conditions

Sepsis, Septic Shock

Keywords

Microcirculation, Remote ischemic conditioning, Sepsis

Brief summary

This study is an evaluation of the effect of Remote ischemic conditioning on sublingual microcirculation in patients with sepsis.

Detailed description

This prospective open-label trial is performed in mixed ICU in a tertiary teaching hospital. Investigators include patients with sepsis or septic shock within the first 24 h after ICU admission. Remote ischemic conditioning (RIC) procedure comprise three repetitions of brachial cuff inflation to 200 mmHg for five minutes following deflation to 0 mmHg for another five minutes. The procedure overall took 30 minutes. RIC is performed at inclusion and repeated 12 h and 24 h later. Sublingual microcirculatory measurements are obtained before and after each RIC procedure, using incidence dark field (IDF) device.

Interventions

PROCEDURERemote ischemic conditioning

Remote ischemic conditioning (RIC) procedure comprise three repetitions of brachial cuff inflation to 200 mmHg for five minutes following deflation to 0 mmHg for another five minutes. The procedure overall took 30 minutes.

Sponsors

Lithuanian University of Health Sciences
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with sepsis or septic shock within the first 24 h after ICU admission.

Exclusion criteria

* age \< 18 years, * pregnancy, * advanced malignancy, * peripheral artery disease affecting both arms, * oral mucosal inflammation or injury or technical difficulties in obtaining sublingual images.

Design outcomes

Primary

MeasureTime frameDescription
Microvascular flow index (MFI) and Proportion of perfused small vessels (PPV)30 minutesThe differences in MFI and PPV between pre- and post-RIC performance.

Countries

Lithuania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026