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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01267318
Other study ID # RD-301
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date January 2011
Est. completion date December 2011

Study information

Verified date July 2012
Source Medtronic - MITG
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Development of a new diagnostic detection tool for gastrointestinal bleeding.


Description:

Literature does not support enough data/knowledge regarding stomach bleeding Hb levels in pathological situations and/or stomach bleeding levels following biopsy. It is important to understand the approximate concentration level of stomach bleeding before proceeding with technology development to insure this technology is capable of detecting such blood levels.


Recruitment information / eligibility

Status Terminated
Enrollment 5
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Male or female subjects = 18 years old.

- Subject is scheduled for EGD endoscopy which includes biopsy, or,

- Subject is scheduled for EGD endoscopy following a bleeding event.

Exclusion Criteria:

- Subject is either not competent or not willing to provide written informed consent.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel RAMBAM Medical Center Haifa

Sponsors (1)

Lead Sponsor Collaborator
Medtronic - MITG

Country where clinical trial is conducted

Israel, 

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