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Updated: May 11, 2026

Murine Endoscopy for In Vivo Multimodal Imaging of Carcinogenesis and Assessment of Intestinal Wound Healing and Inflammation
Published on: August 26, 2014
A multicenter, prospective, randomized comparison of a novel signal transmission capsule endoscope to an existing
Eric H Choi1, Klaus Mergener, Carol Semrad
1Division of Gastroenterology and Hepatology, Riverside Medical Clinic, Riverside, California, USA.
Background:
MiroCam, a capsule endoscope, uses a novel transmission technology, electric-field propagation, which uses the human body as a conduction medium for data transmission.
Objective:
To compare the ability of the MiroCam (MC) and PillCam (PC) to identify sources of obscure GI bleeding (OGIB).
Design:
Prospective, multicenter, comparative study.
Setting:
Six academic hospitals.
Patients:
A total of 105 patients with OGIB.
Intervention:
Patients ingested both the MC and PC capsules sequentially in a randomized fashion.
Main Outcome Measurements:
Concordance of rates in identifying a source of OGIB, operational times, and rates of complete small-bowel examination.
Results:
Data analysis resulted in 43 (48%) "abnormal" cases identifying a source of OGIB by either capsule. Twenty-four cases (55.8%) were positive by both capsules. There was negative agreement in 46 of 58 cases (79.3%). The κ index was 0.547 (χ(2) = 1.32; P = .36). In 12 cases, MC positively identified a source that was not seen on PC, whereas in 7 cases, PC positively identified a source that was not seen on MC. MC had a 5.6% higher rate of detecting small-bowel lesions (P = .54). MC captured images at 3 frames per second for 11.1 hours, and PC captured images at 2 frames per second for 7.8 hours (P < .0001). Complete small-bowel examination was achieved in 93.3% for MC and 84.3% for PC (P = .10).
Limitations:
Readers were not blinded to the particular capsule they were reading.
Conclusion:
A positive diagnostic finding for OGIB was identified by either capsule in 48% of cases. The concordance rate between the 2 capsules was comparable to that of prior studies in identifying sources of small-bowel bleeding. The longer operational time of the MC may result in higher rates of complete small-bowel examination, which may, in turn, translate into a higher rate of detecting small-bowel lesions. (
Clinical Trial Registration Number:
NCT00878982.).
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