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Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected

Prospective Assessment of Anastomotic Leak

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02178228
Enrollment
1077
Registered
2014-06-30
Start date
2013-10-31
Completion date
2018-01-31
Last updated
2018-02-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anastomotic Leaks

Keywords

Anastomotic Leaks, Bowel Resection, Postoperative Complication

Brief summary

The purpose of this study is to identify the cause of leaks that sometimes occur after a section of the bowel is removed and reconnected. Certain staplers from the operating room will be collected and sent to a third party (ECRI Institute) to be examined for defects. The patient's charts will be analyzed for medical issues that may contribute to leaks after surgery.

Detailed description

The objective of this study is to identify peri-operative factors that contribute to leaks after a portion of the bowel has been cut and reconnected. Most specifically, the role of staplers in this reconnection of the bowels will be evaluated. The research will take place at Icahn School of Medicine where there is an extremely high volume of operations involving small bowel and large bowel being cut and reconnected. Patients will be recruited based on inclusion and exclusion criteria and 500 subjects are expected to be enrolled in the study. The surgery will be performed in a standard fashion as indicated by diagnosis, location of disease, patient condition, and surgeon preference. No changes to the surgical procedure will be mandated by the research protocol. This is purely an observational study with no changes to the standard of care. The patients will be followed throughout the course of the their hospital stay for the scheduled surgery up to one week and one month after the procedure to gather laboratory data and any complications incurred due to the surgery. No patient specimen will be stored. The staplers used in the procedure will be collected, stored in sterile plastic container, information about the staplers will be recorded, and then discarded after 30 days in the usual manner that the operating room staff employs to discard the staplers. Subjects lost to follow-up after the procedure will be withdrawn from the study.

Interventions

None listed

Sponsors

ECRI Institute
CollaboratorUNKNOWN
Medtronic - MITG
CollaboratorINDUSTRY
Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subject must be scheduled for non-emergent small or large bowel surgery and reconnection of bowel at Icahn School of Medicine at Mount Sinai * Subjects must be able and willing to provide informed consent * Subjects must be 18 years or above OR 15-17 with permission of one parent * English and Spanish speaking patients will be included in this study

Exclusion criteria

* Subject who are less than 15 years of age * Subject who are scheduled for emergent surgery, precluding the capacity to give informed consent * Subjects who are diagnosed with obstructed or perforated colon cancer

Design outcomes

Primary

MeasureTime frame
All cause bowel leaks after surgeryone week post-operation

Secondary

MeasureTime frame
Reoperation1 year post operation
Sepsis1 year post operation
Length of hospital stay1 year post operation
Mortality1 year post operation

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026