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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04996511
Other study ID # Q021
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2020
Est. completion date December 31, 2024

Study information

Verified date February 2024
Source Joint Authority for Päijät-Häme Social and Health Care
Contact Juha KA Rinne, MD
Phone 03 81911
Email juha.rinne@phhyky.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

HRV measurement of patients recovering from laparoscopic colorectal resection for any pathology.


Description:

Patients scheduled for colorectal surgery are recruited to the study. HRV parameters including e.g. RMSSD are evaluated before and after surgery. The effect of surgery and possible complications associated with it on parameters and relationship with specific adverse effects caused by complications are evaluated.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date December 31, 2024
Est. primary completion date May 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: • Colorectal resection for any pathology Exclusion Criteria: • Arrhytmias likely to cause problems with HRV measurements

Study Design


Related Conditions & MeSH terms


Intervention

Device:
PulseOn
Postoperative HRV measurement

Locations

Country Name City State
Finland Päijät-Häme Central Hospital Lahti

Sponsors (2)

Lead Sponsor Collaborator
Joint Authority for Päijät-Häme Social and Health Care Tampere University

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Heart Rate Variability (HRV) change Reliability of HRV parameters 3 days
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