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Membrane Shedding During Severe Sepsis and Septic Shock: Pathophysiological and Clinical Relevance

Membrane Shedding During Severe Sepsis and Septic Shock: Pathophysiological and Clinical Relevance

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02391792
Enrollment
300
Registered
2015-03-18
Start date
2013-03-31
Completion date
2020-03-31
Last updated
2016-08-24

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

Conditions

Severe Sepsis and Septic Shock

Brief summary

Microparticules (MPs) result from plasma cell membrane remodeling and shedding after cell stimulation or apoptosis. MPs are know recognized as a pool of bioactive messengers with merging role in pathophysiology of immune and cardiovascular diseases. MPs have been characterized during septic shock and may contribute to dissemination of pro-inflammatory and procoagulant mediators. This a prospective observational study of circulating MPs and blood coagulation in septic shock patients admitted in medical intensive care units (ICUs) of four tertiary hospitals at baseline (D1, D2, D3, D4, D7).

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Septic shock (patients) * Without septic shock (control) * Informed consent

Exclusion criteria

* Class IV heart failure * Child-plugh grade C cirrhosis * Cancer under active treatment * BMI\>35kg/m2 * Moribund patient * DNR decision

Design outcomes

Primary

MeasureTime frame
Change from baseline in number and type of circulating microparticles at 7 daysBaseline and 7 days
Change from baseline in blood coagulation markers at 7 daysBaseline and 7 days

Countries

France

Contacts

Primary ContactFerhat MEZIANI, MD, PhD
ferhat.meziani@chru-strasbourg.fr

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026