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Clinical Trials/NCT04996511
NCT04996511RecruitingNot Applicable

Day Case Colectomy: Optimizing Short Stay-surgery.

Joint Authority for Päijät-Häme Social and Health Care2 sites in 1 country30 target enrollmentStarted: January 1, 2020Last updated:
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Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
30
Locations
2
Primary Endpoint
Heart Rate Variability (HRV) change
Study OverviewStudy DesignEligibility CriteriaArms & InterventionsOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

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

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to 100 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Colorectal resection for any pathology

Exclusion Criteria

  • •Arrhytmias likely to cause problems with HRV measurements

Arms & Interventions

Colorectal Surgery Patients

Experimental

Intervention: PulseOn (Device)

Outcomes

Primary Outcomes

Heart Rate Variability (HRV) change

Time Frame: 3 days

Reliability of HRV parameters

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Joint Authority for Päijät-Häme Social and Health Care
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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Day Case Colectomy: Optimizing Short... | Clinical Trial