Evaluation of a wrist-worn photoplethysmography monitor for heart rate variability estimation in patients recovering from laparoscopic colon resection.
Juha K A Rinne, Seyedsadra Miri, Niku Oksala...
https://pubmed.ncbi.nlm.nih.gov/35394583Actively Recruiting
Phase Not Applicable
Age: 18Years - 100Years
All Genders
ID04996511
Day Case Colectomy: Optimizing Short Stay-surgery.
Led by Joint Authority for Päijät-Häme Social and Health Care · Updated on 2026-04-22
30
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
Sponsors
J
Joint Authority for Päijät-Häme Social and Health Care
Lead Sponsor
T
Tampere University
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research focuses on patients undergoing laparoscopic colorectal surgery for various conditions. It aims to evaluate heart rate variability (HRV) parameters, such as RMSSD, before and after surgery to understand how surgical effects and possible complications impact these measurements and relate to specific adverse outcomes. Participants receive standard colorectal surgery followed by monitoring using the PulseOn device to measure HRV after the operation. The study specifically examines changes in HRV within three days post-surgery to assess recovery and complications. During the study, participants' HRV is tracked before and after surgery, with data collected via the PulseOn device. Researchers monitor HRV changes and complications to evaluate recovery quality. The total participation involves preoperative and postoperative assessments focused on physiological monitoring within the first few days after surgery.
CONDITIONS
Brief Title
Day Case Colectomy: Optimizing Short Stay-surgery.
Who Can Participate
Age: 18Years - 100Years
All Genders
Eligibility Criteria
You may qualify if you...
- Colorectal resection for any pathology
You will not qualify if you...
- Arrhythmias likely to cause problems with HRV measurements
AI-Screening
AI-Powered Screening
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1
2
3
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Surgery and Immediate Post-operative Care
Duration - 3 days
Participants undergo colorectal surgery and have heart rate variability (HRV) measurements taken to assess the effect of surgery and possible complications.
1 surgery day visit and postoperative HRV monitoring
Trial Site Locations
Total: 1 location
1
Päijät-Häme Central Hospital
Lahti, Finland, 15850
Actively Recruiting
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Research Team
J
Juha KA Rinne, MD
J
Jyrki AO Kössi, Adjunct.Prof
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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