An observational study in Acute Pancreatitis and Organ Failure, Multiple, sponsored by Nanjing University School of Medicine. Status unknown. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-11-27.
Sponsored by Nanjing University School of Medicine · Observational
In this study, the investgatiors aimed to investigate the associations between serum levels of stearoyl-CoA desaturase-1（SCD-1） and the disease severity as well as the presence of adverse clinical events, such as local complications, organ failure, mortality and so on.In this prospective study, participants were divided into two groups based on serum SCD-1 concentration on admission and prospectively observe the disease severity and clinical outcomes of them.
557 studies on the registry are indexed under Pancreatitis; 164 are open to participants now.
This study's planned enrollment of 216 is close to the median of 200 across 192 observational studies indexed under Pancreatitis.
Browse Pancreatitis studies →Nanjing University School of Medicine is the lead sponsor of 39 studies on the registry; 5 are open to participants now.
Counted across the registry records on this site, refreshed daily.
patients with the diagnosis of acute pancreatitis (Atlanta standard), abdominal pain occurred within one week of admission; we intended to include the severer cases (APACHEII score is more than 8 and Ranson score is greater than 3).
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
the incidence rate of infected pancreatic necrosis
Time frame: 2-4 week after disease onset
the incidence rate of organ failure
the incidence rate of organ failure (transient or persistent)
Time frame: 1-2 week after disease onset
the incidence rate of local complications
acute peripancreatic fluid collections, pancreatic pseudocycts, acute necrotic collections and walled-off necrosis
Time frame: 1-2 week after disease onset
No study locations are listed for this record.
This study is status unknown, as verified in Nov 2017. You cannot join it, but the record below documents what was studied.
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Nanjing University School of Medicine