Clinical Trials Directory

Trials / Unknown

UnknownNCT02691598

Dexmedetomidine Hydrochloride in the Prevention of Organ Failure Following Severe Acute Pancreatitis

Dexmedetomidine Hydrochloride in the Prevention of Organ Failure Following

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
314 (estimated)
Sponsor
Nanjing University School of Medicine · Academic / Other
Sex
All
Age
15 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Cytokines such as such as TNF-a, IL-1, IL-6 correlate with the severity of pancreatitis.Neuroendocrine pathways, such as the sympathetic nervous system or parasympathetic nervous system, in turn, have some impact on the immune systems, through a-2 adrenoreceptor stimulation or the cholinergic anti-inflammatory pathway. The investigators aim to use Dexmedetomidine Hydrochloride to decrease the activity of sympathetic nervous system, thus relieve inflammation response.

Detailed description

Infected pancreatic necrosis (IPN) and multiple organ dysfunction syndrome (MODS) are major complications of acute pancreatitis which determine disease severity and outcome.It is concluded that systemic inflammation in SAP characterized by the endocrine release of different cytokines, such as TNF-a, IL-1, IL-6 and many others. These cytokines correlate with the severity of pancreatitis. Neuroendocrine pathways, such as the sympathetic nervous system or parasympathetic nervous system, in turn, have some impact on the immune systems, through a-2 adrenoreceptor stimulation or the cholinergic anti-inflammatory pathway. Dexmedetomidine Hydrochloride is a high selected a-2 adrenoreceptor agonists.Some studies have shown that Dexmedetomidine Hydrochloride could improve the outcome of sepsis patients and decrease the development of organ failure. The investigators aim to use Dexmedetomidine Hydrochloride to decrease the activity of sympathetic nervous system,thus relieve inflammation response.

Conditions

Interventions

TypeNameDescription
DRUGInfusionDexmedetomidine Hydrochloride or normal saline 4ug/ml;0.05ml/kg.h infusion for 24hours

Timeline

Start date
2016-02-01
Primary completion
2016-02-01
Completion
2017-08-01
First posted
2016-02-25
Last updated
2016-02-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02691598. Inclusion in this directory is not an endorsement.