Day Case Colectomy: Optimizing Short Stay-surgery.

Joint Authority for Päijät-Häme Social and Health Care

Status: Enrolling

Conditions: Monitoring, Physiologic

Treatments: Device: PulseOn

Study type: Interventional

Funder types: Other

Identifiers

NCT04996511

Q021

Details and patient eligibility

About

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

Full 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.

Enrollment: 10 estimated patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Colorectal resection for any pathology

Exclusion criteria

• Arrhytmias likely to cause problems with HRV measurements

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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10 participants in 1 patient group

Colorectal Surgery Patients

Experimental group

Treatment:

Device: PulseOn