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Evaluation of the Ability to Detect Bowel Gas During Laparoscopic Surgery

Evaluation of the Ability to Detect Bowel Gas During Laparoscopic Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02679118
Enrollment
8
Registered
2016-02-10
Start date
2016-02-29
Completion date
2016-06-30
Last updated
2017-08-18

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

Conditions

Intestinal Perforation

Keywords

intestinal perforation, bariatric surgery, gastric bypass, gastric perforation, colonic perforation

Brief summary

This study will determine the ability of the device to draw a small amount of gas from an insufflated abdomen during laparoscopic surgery and accurately detect if gaseous content from the bowel is present.

Detailed description

Undetected bowel perforation is a rare but dangerous complication of laparoscopic surgery. If the injury is not detected and treated at the time of the surgical procedure, the patient can suffer sever complications including septic shock and eventually death. Our goal is to test a novel device that can detect bowel gas leakage from a perforation and alert the surgeon during the operation by evaluating the gases present in the insufflated abdomen during surgery. During laparoscopic surgery, carbon dioxide in inserted in the abdominal cavity in order to perform the operation. This is dynamic process as insufflation is a constant during the entire procedure to maintain a constant pressure and compensate small leaks due to the insertion and retrieval of instruments. This study will determine the ability of device to be attached to a standard Veress needle or trocar during the operation and periodically draw a small amount of gas from the abdomen to evaluate the gas and accurately detect gaseous content from the bowel. Before the device can be used to detect bowel perforations, first we must ensure that it can accurately detect bowel gas in an insufflated abdomen.

Interventions

DEVICESentire

The device, at predetermined time points, will draw a small amount of gas from the abdomen. Upon obtaining the samples, the machine will analyze the sample for evidence of bowel gas. After each sample, the device will be purged prior to the acquisition of the next gas sample. The results of the analysis of the gas samples will be recorded for future analysis.

Sponsors

Dan E. Azagury
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE

Eligibility

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

Inclusion criteria

1. Age 18 - 60 years old with the diagnosis of morbid obesity, who qualifies for laparoscopic gastric bypass surgical therapy, and has elected to undergo laparoscopic gastric bypass surgery. 2. Receiving care in the Stanford Hospital General Surgery Bariatric Surgery Clinic under the care of Dr. Dan Azagury 3. The patient is scheduled for laparoscopic roux en y gastric bypass surgery, with Dr. Azagury. 4. Willing and cognitively able to sign informed consent.

Exclusion criteria

1. Lack of or inability to provide informed consent. 2. Less than 18 years of age or greater than 60 years of age 3. Planned deviation from the standard laparoscopic gastric bypass operation 4. Conversion intra-operatively from a laparoscopic gastric bypass to an alternative laparoscopic surgical operation or to an open gastric bypass operation. 5. Enrollment in another device or drug study that may confound results.

Design outcomes

Primary

MeasureTime frameDescription
Methane levels released in the abdominal cavity from small bowelIntra-operative measurement onlyAbility to detect and measure the level of methane released in the abdominal cavity by open small bowel
Hydrogen levels released in the abdominal cavity from small bowelIntra-operative measurement onlyAbility to detect and measure the level of hydrogen released in the abdominal cavity by open small bowel

Countries

United States

Outcome results

None listed

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