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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT01941472
Other study ID # MICU2013-1
Secondary ID
Status Not yet recruiting
Phase N/A
First received August 31, 2013
Last updated September 9, 2013
Start date September 2013

Study information

Verified date September 2013
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Fluid challenge is often carried out in critical ill patients. Its responsiveness usually requires invasive monitoring. To use non-invasive methods is very tempting. We hypothesize that transcutaneous pO2,transcutaneous pCO2 and Central Venous pO2 variations provide feasible estimation on fluid responsiveness in critical ill patients.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years and older ICU patients;

- Hypotension or shock;

- Monitored with PICCO or Swan-Ganz catheter;

- The decision of fluid challenge made by the treating physician;

Exclusion Criteria:

- Evidence of fluid overload;

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Screening


Related Conditions & MeSH terms


Intervention

Other:
fluid administration


Locations

Country Name City State
China MICU of Peking Union Medical College Hospital Beijing Beijing
China MICU of Peking Union Medical College Hospital Peking Beijing

Sponsors (1)

Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Area Under Roc Curve About one year No
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