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Dexmedetomidine on Microcirculation in Septic Shock

Dexmedetomidine Improve Microcirculatory Alterations in Initial Resuscitated Septic Shock Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02270281
Enrollment
44
Registered
2014-10-21
Start date
2014-12-31
Completion date
2017-05-31
Last updated
2018-12-12

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

Conditions

Septic Shock

Keywords

Sepsis, Sedation, Microcirculation, Dexmedetomidine

Brief summary

Dexmedetomidine was found might be beneficial to sepsis. Dexmedetomidine were found to improve microcirculation in sepsis animal studies and non-sepsis patients. However, the effect of dexmedetomidine on microcirculation in septic shock patients is unknown.

Detailed description

Septic shock is characterized by significant decline in vascular response and relative hypovolemia. Fluids and exogenous catecholamines are mainstay. However, even after initial resuscitation, microcirculatory dysfunctions still exist, and represent a direct physiologic link to organ failure and death. Therefore, therapeutic strategies aiming at improving microcirculation are performed. Dexmedetomidine was found might be beneficial to sepsis. Dexmedetomidine were found to improve microcirculation in sepsis animal studies and non-sepsis patients. However, the effect of dexmedetomidine on microcirculation in septic shock patients is unknown. Based on the hypothesis that dexmedetomidine might improve microcirculation in initial resuscitated septic shock patients, the study was to investigate the effects of dexmedetomidine on microcirculation in early septic shock patients despite initial resuscitation. Meanwhile, to observe the possible mechanism of the effect, the correlation between dexmedetomidine dose and microcirculatory parameters as well as catecholamine level were performed.

Interventions

DRUGDexmedetomidine 0.7 Mcg/kg/h

CIF 0.7mcg/kg/h

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

Adult patients who met the following inclusion criteria were enrolled in the study: 1) With septic shock defined by the 2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference for less than 24 hours. 2\) After initial fluid resuscitation but still requiring norepinephrine to maintain arterial pressure or hyperlactacidemia. 3\) Need ongoing analgesia and sedation. 4) Using advanced invasive hemodynamic monitoring techniques.

Exclusion criteria

were as follows: 1. age less than 18 years. 2. pregnancy. 3. heart rate less than 55 beats per minute. 4. acute hepatic failure 5. brain injury.

Design outcomes

Primary

MeasureTime frameDescription
Perfused vascular densityOne hourPerfused vascular density was calculated by multiplying vessel density by the proportion of perfused vessels

Secondary

MeasureTime frameDescription
Microcirculatory flow indexOne hourBased on the major type of flow in all quadrants were determined with a semi-quantitative methodology
Total vascular densityOne hourVascular density was calculated by the number of vessels crossing these lines

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026