Pulse Waveform and ECG Analysis in Postoperative Cardiac Surgical Patients

Blood Pressure Clinical Trial

Official title:

Pulse Waveform and ECG Analysis in Postoperative Cardiac Surgical Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02350608
• Other study ID #: R14013
• 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

• Arrhythmias, Cardiac
• Blood Pressure

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