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Clinical Trials/NCT01982708
NCT01982708
Completed
N/A

A Prospective Study of a Haptic Device Evaluation of the Acute Abdomen

Michigan State University1 site in 1 country20 target enrollmentDecember 2013
ConditionsAcute Abdomen

Overview

Phase
N/A
Intervention
Not specified
Conditions
Acute Abdomen
Sponsor
Michigan State University
Enrollment
20
Locations
1
Primary Endpoint
Hardness of the abdominal wall
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The study hypothesis is a haptic sensor can aid in the evaluation of the acute abdomen. Investigators from the MSU Department of Surgery in Collaboration with MSU Engineering are assessing the ability of a non invasive, optical device that is placed on a patients abdomen (much like an ultrasound transducer) to evaluate a patient with an acute abdominal presentation. Conditions such as appendicitis, cholecystitis, diverticulitis or small bowel obstruction will be examined with the haptic device. Data will be collected by the device and later compared to the abdominal findings recorded from an examination conducted by the principle investigator who is a surgeon. The surgeon will not have acess to data collected by the haptic sensor and therefore it will have no impact on the decision making process in the care of the patient. The impact on the individual patient will require obtaining a consent to participate in the study, a few minutes to place the device gently on the abdomen and collect the sensor data. There is no direct benefit to the patient by participating in the study. The potential for such a study may be to develop the technology to have a device that non-medical staff can use to collect patient data and transmit that data to a healthcare provider at another location.

Registry
clinicaltrials.gov
Start Date
December 2013
End Date
June 2014
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Robert Osmer

MSU Surgeon

Michigan State University

Eligibility Criteria

Inclusion Criteria

  • All patients referred to the MSU Acute Care Surgery service for the evaluation of abdominal pain.

Exclusion Criteria

  • Under 18 years of age

Outcomes

Primary Outcomes

Hardness of the abdominal wall

Time Frame: At intial presentation with abdominal pain

Secondary Outcomes

  • temperature of the abdominal wall(At initial presentation)

Study Sites (1)

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