Serum Maresin-1 Predicts the Severity of Severe Acute Pancreatitis
Serum Maresin-1 Level Predicts the Disease Severity and Clinical Outcomes of Severe Acute Pancreatitis Patients
Study Overview
Status
Status
Conditions
Conditions
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Weiqin Li
- Phone Number: 13962531994
- Email: luyingying126@sina.cn
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Clinical diagnosis of Severe Acute Pancreatitis
- Biliary pancreatitis
- 7 days of the onset
Exclusion Criteria:
- Surgical patients
- Serious diseases and infection
- Alcoholic pancreatitis
- Hypertriglyceridemia pancreatitis
- Disorder of Glucolipide Metabolism:diabetes mellitus, hypertriglyceridemia, BMI>30
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Retrospective
Number of groups / cohorts
Cohorts and Interventions
Group / CohortGroup / Cohort |
|---|
|
normal level of serum maresin-1
|
|
abnormal level of serum maresin-1
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
mortality
Time Frame: up to 28 days
|
The level of serum maresin-1 predicts the severity of severe acute pancreatitis
|
up to 28 days
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The incidence of MODS
Time Frame: through study completion, an average of 1 year
|
The level of serum maresin-1 predicts the severity of severe acute pancreatitis
|
through study completion, an average of 1 year
|
|
The incidence of IPN
Time Frame: through study completion, an average of 1 year
|
The level of serum maresin-1 predicts the severity of severe acute pancreatitis
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Anticipated)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- SMPSSAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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