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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02691598
Other study ID # DHPOFFSAP1
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received February 14, 2016
Last updated February 20, 2016
Start date February 2016
Est. completion date August 2017

Study information

Verified date February 2016
Source Nanjing University School of Medicine
Contact Weiqin Li, M.D.
Phone +8613182810702
Email liweiqindr@vip.163.com
Is FDA regulated No
Health authority China: Chinese Medical Association
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 314
Est. completion date August 2017
Est. primary completion date February 2016
Accepts healthy volunteers No
Gender Both
Age group 15 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients diagnosed with severe acute pancreatitis within 48h

- APACHE II=8

- Patients or the family agreed to receive the treatment, and signed the informed consents

Exclusion Criteria:

- Patients were allergy to the drug

- Patients were diagnosed with Arrhythmia

- Patients with artificial permanent pacemaker implantation

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Drug:
Infusion
Dexmedetomidine Hydrochloride or normal saline 4ug/ml;0.05ml/kg.h infusion for 24hours

Locations

Country Name City State
China Department of SICU, Research Institute of General Surgery Jinling Hospital, Nanjing, Jiangsu, China Nanjing Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Nanjing University School of Medicine

Country where clinical trial is conducted

China, 

References & Publications (1)

Zhang L, Zhou J, Ke L, Nie Y, Tong Z, Li W, Li J. Role of heart rate variability in predicting the severity of severe acute pancreatitis. Dig Dis Sci. 2014 Oct;59(10):2557-64. doi: 10.1007/s10620-014-3192-5. Epub 2014 May 13. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence rate of Organ failure 30 days after Incidence of the disease Yes
Secondary Infected pancreatic necrosis 30 days after Incidence of the disease Yes
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