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NCT00933751 Clinical Trial

Changes of Oxygen Saturation in Inferior Vena Cava (IVC) in Patients During and After High Risk Abdominal Surgery and Relationship to the Outcome

Abdominal Surgery Clinical Trial

Official title:
Changes of Oxygen Saturation in Inferior Vena Cava (IVC) in Patients During and After High Risk Abdominal Surgery and Relationship to the Outcome.

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT00933751
Other study ID # 100/09
Secondary ID
Status Not yet recruiting
Phase N/A
First received July 5, 2009
Last updated April 4, 2011
Start date July 2009

Study information
Verified date July 2009
Source Assaf-Harofeh Medical Center
Contact Zoya Haitov, MD
Phone 089778080
Email ZoyaC@asaf.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Tissue hypoxia is one of the most important factors leading to the development of multiorgan failure. Patients presenting for emergent major abdominal surgery might suffer from organ hypoperfusion. Thus, early detection of the imbalance between oxygen supply and demand may improve the outcome. The investigators believe that hypoperfusion of the abdominal organs will cause a decrease of the saturation in the hepatic vein and in the IVC.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 20
Est. completion date
Est. primary completion date August 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All consecutive patients presenting for emergency surgery due to acute abdomen pain

- Older than 18 years old

- Not pregnant

Exclusion Criteria:

- Age < 18

- Pregnancy

- Major coagulopathy

- Permanent pacemaker

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Device:
• Central vein catheterization
Blood samplings from IVC catheter

Locations
Country Name City State
Israel Assaf-Harofeh MC Beer-Yaakov

Sponsors (1)
Lead Sponsor Collaborator
Assaf-Harofeh Medical Center

Country where clinical trial is conducted

Israel, 

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