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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02350608
Other study ID # R14013
Secondary ID
Status Completed
Phase N/A
First received January 26, 2015
Last updated November 3, 2015
Start date March 2015
Est. completion date November 2015

Study information

Verified date November 2015
Source Tampere University Hospital
Contact n/a
Is FDA regulated No
Health authority Finland: Valvira - National Supervisory Authority for Welfare and Health
Study type Observational

Clinical Trial Summary

Observational study of 20 postoperative cardiac surgery patients. On admission to the ICU the patients will receive a noninvasive monitor recording arterial pulse waveform and ECG. The monitoring will continue to the ward for two days. The data will be compared with the routine monitoring methods.


Description:

Observational study of 20 adult postoperative cardiac surgery patients. The observation will last from 0 to 2. postoperative day. On admission to the ICU the patients will receive a noninvasive monitor recording arterial pulse waveform and ECG. The monitoring will continue to the ward for two days. The data will be compared with the routine monitoring methods in the ICU and the ward.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult cardiac surgery patients, informed consent

Exclusion Criteria:

- Poor co-operation, age less than 18 years

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Noninvasive monitor
A novel technique on noninvasive blood pressure monitoring.

Locations

Country Name City State
Finland Tampere University Hospital Heart Center Tampere

Sponsors (1)

Lead Sponsor Collaborator
Tampere University Hospital

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Detection of arrythmia 2 days No
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