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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06227871
Other study ID # 11894
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2019
Est. completion date March 1, 2023

Study information

Verified date January 2024
Source Kern Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to compare the presentation, treatment, and outcomes in patients suffering traumatic pancreatic injuries from blunt or penetrating trauma. The questions this study aims to answer are: 1. Does a statistically significant association exist between pancreatic injury grade and the following individual factors: - Mortality - Morbidity - Injury severity score 2. Is there an association between post-operative pancreatic complications and operation-specific intervention? 3. Does pancreatic injury score correlate with certain intra-abdominal organ injuries? Participants meeting criteria are greater than 18 years old, with no history of pancreatic surgery who were hospitalized at Kern Medical Center after presenting to the institution's emergency department as tier 1 or 2 trauma activations following blunt or penetrating abdominal injury and were diagnosed with pancreatic injury during the same hospitalization.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date March 1, 2023
Est. primary completion date March 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Hospitalized at Kern Medical Center after presenting to the institution's emergency department as a tier 1 and 2 trauma activation - Hospitalized following blunt or penetrating abdominal injury - Diagnosed with traumatic pancreatic injury during same admission Exclusion Criteria: - history of pancreatic surgery - Iatrogenic pancreatic injuries

Study Design


Intervention

Procedure:
Exploratory laparotomy
Exploratory laparotomy with interventions addressing pancreatic injuries Grade 1-5 including pancreatic interventions including subtotal pancreatectomy, distal pancreatectomy, pancreatic ligation, pyloric diversion, or simple drainage of the pancreas.

Locations

Country Name City State
United States Kern Medical Center Bakersfield California

Sponsors (1)

Lead Sponsor Collaborator
Kern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complication occurrence Complications including wound dehiscence, pancreatic duct leak, pancreatic pseudocyst, pancreatic fistula formation, pancreatic necrosis, intra-abdominal abscess, traumatic pancreatitis, anastomotic leak Up to 12 weeks postoperatively
Secondary Associated intra-abdominal injuries concomitant intra-abdominal injuries including pancreatic duck, diaphragm, stomach, liver, kidney, Major vasculature, spleen, duodenum, small bowel, colon, ureter within 48 hours of admission
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