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OpenTrials
Completed

NCT Number: NCT02178228

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

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.

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Key information

Age range

15 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Icahn School of Medicine at Mount Sinai

New York, 10029, United States

About this study

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 Subjects lost to follow-up after the procedure will be withdrawn from the study.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Primary outcomes

  1. All cause bowel leaks after surgery

    Time frame: one week post-operation

  2. All cause bowel leaks after surgery

    Time frame: one month post-operation

Secondary outcomes

  1. Reoperation

    Time frame: 1 year post operation

  2. Sepsis

    Time frame: 1 year post operation

  3. Length of hospital stay

    Time frame: 1 year post operation

  4. Mortality

    Time frame: 1 year post operation

Sponsors and collaborators

Lead sponsor

Icahn School of Medicine at Mount Sinai

Other

Collaborators

  • ECRI Institute
  • Medtronic - MITG

Registry information

Official study title

Prospective Assessment of Anastomotic Leak

Important dates

Study start
2013
Primary completion
2018
Study completion
2018
First posted
Jun 30, 2014
Registry last updated
Feb 5, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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