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Clinical Trials/NCT06223620
NCT06223620
Completed
Not Applicable

A Multicenter Retrospective Review of Management Strategies in Small Bowel Obstruction

Methodist Health System1 site in 1 country504 target enrollmentStarted: July 30, 2018Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
504
Locations
1
Primary Endpoint
Morbidity and length of stay

Overview

Brief Summary

The objective of the study is to review performance of water soluble contrast study in patients admitted with Small Bowel Obstruction(SBO), will improve quality and safety, and decrease length of stay and morbidity.

Detailed Description

Performance of contrast study has been a part of the protocols at multiple institutions of the southwestern surgical congress. Plan to perform a retrospective review of management protocols at these institutions. Wish to know whether the implementation of a standardized, protocol-driven pattern of practice involving the performance of water soluble contrast study in patients admitted with SBO, will improve quality and safety, and decrease length of stay and morbidity.

The objective of the study is to review performance of water soluble contrast study in patients admitted with SBO, will improve quality and safety, and decrease length of stay and morbidity.

Performance of contrast study has been a part of the protocols at multiple institutions of the southwestern surgical congress.

Hypothesize that implementation of a standardized, protocol-driven pattern of practice involving the performance of water soluble contrast study in patients admitted with SBO, will improve quality and safety, and decrease length of stay and morbidity.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 89 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • • Adults aged 18-89 years of age
  • Patients presenting with SBO

Exclusion Criteria

  • • Prisoners
  • Pregnant women

Outcomes

Primary Outcomes

Morbidity and length of stay

Time Frame: 1 year

Morbidity and length of stay

Secondary Outcomes

  • Aspirin(ASA )class(1 year)
  • time of contrast given(1 year)
  • admit date(1 year)
  • comorbidities(1 year)
  • labs(1 year)
  • Patient demographics(1 year)
  • discharge date(1 year)
  • admission service(1 year)
  • surgical history(1 year)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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