Trial Details

Not Recruiting
Basic Information
Clinical ID c2555
Identifier ACTRN12620000322932
Trial Title The hospital costs associated with postoperative complications following small bowel resection surgery: a cohort study
Trial URL Visit Original Page
Study Information
Study Results

Yes

Conditions Small bowel resection;Complications following small bowel resection;Inflammatory Bowel Disease;Small Bowel Cancer; Small bowel resection Complications following small bowel resection Inflammatory Bowel Disease Small Bowel Cancer;Surgery - Surgical techniques;Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon;Oral and Gastrointestinal - Inflammatory bowel disease;Anaesthesiology - Anaesthetics;Cancer - Bowel - Small bowel (duodenum and ileum)
Interventions There is no participant involvement. Only the de-identified hospital medical record of patients who have undergone surgery will be reviewed. We will review the following ICD Codes: 30515-03 Ileocolic resection with anastomosis 30515-04 Laparoscopic ileocolic resection with anastomosis 30515-05 Ileocolic resection with formation of stoma 30515-06 Laparoscopic ileocolic resection with formation of stoma 30565-00 Resection of small intestine with formation of stoma 30566-00 Resection of small intestine with anastomosis The procedures were performed at the Austin Hospital, a tertiary hospital with small bowel expertise, over the period of January 2013 and June 2018. Patients were followed-up for 30 days following discharge from the index admission. If no subsequent re-admissions occurred within this period, follow-up ceased. If a patient was readmitted within the 30-day period, then the readmission was included, and following discharge from the readmission or end of the original 30-day period, whichever was later, follow-up ceased.
Participant Information
Sponsor Department of Anaesthesia, Austin Health
City -
Country/Region Australia
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, ELDER, OLDER_ADULT
Study Design
Study Type Observational
Phase Not Available
Time Information
Start Date 2025-04-24
Primary Completion Date 2020-03-09
Completion Date 2020-01-28