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NCT01267318 Clinical Trial

Evaluation of Gastric Juice Samples During Standard Gastroscopy Procedure

Gastrointestinal Bleeding Clinical Trial

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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