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Clinical Trials/NCT04508270
NCT04508270
Completed
Not Applicable

Physiological Evidence for Early Mobilization in Thoracoscopic Lobectomy

Rigshospitalet, Denmark1 site in 1 country24 target enrollmentSeptember 8, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Lung Neoplasm
Sponsor
Rigshospitalet, Denmark
Enrollment
24
Locations
1
Primary Endpoint
Postoperative forced expiratory volume in one second (FEV1)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The main endpoint is physiological rehabilitation after VATS-L under early mobilization. The secondary endpoints are exploring the effect of early mobilization on postoperative physiology.

Investigators hypothesis that early mobilization is clearly advantaged to advance the physiological recovery.

Registry
clinicaltrials.gov
Start Date
September 8, 2020
End Date
December 18, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lin Huang

Medical Doctor, Research fellow, PhD student

Rigshospitalet, Denmark

Eligibility Criteria

Inclusion Criteria

  • VATS lobectomy;
  • Speak and understand Danish or English;
  • Informed consent obtained.

Exclusion Criteria

  • Co-VATS lobectomy (more than one lobe resection);
  • Supplementary oxygen therapy later 6 h after surgery;
  • No willing to wear electronic device;
  • No willing to exam arterial oxygen saturation.

Outcomes

Primary Outcomes

Postoperative forced expiratory volume in one second (FEV1)

Time Frame: Through study completion, an average of 3 days

FEV1 is the amount of air you can force from your lungs in one second. Participants will be examed via spirometer.

Postoperative arterial oxygen saturation.

Time Frame: Through study completion, an average of 3 days

Oxygen saturation is the fraction of oxygen-saturated hemoglobin relative to total hemoglobin (unsaturated + saturated) in the blood. Participants will be tested via oximeter.

Secondary Outcomes

  • The quantization of activity counts(Through study completion, an average of 3 days)
  • The quantization of pain(Through study completion, an average of 3 days)
  • length of stay in hospital(Through study completion, an average of 3 days)
  • Duration of chest tube(Through study completion, an average of 2 days)
  • Postoperative complications(up to 30 days)

Study Sites (1)

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