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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04507594
Other study ID # DiaphragmaticDysfunction
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 6, 2020
Est. completion date October 30, 2022

Study information

Verified date October 2022
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to measure diaphragmatic dysfunction with ultrasonography and nerve stimulation of the phrenicus nerve, in patients undergoing thoracic surgery for lung and esophageal cancer, and correlate measures of diaphramatic function to clinical postoperative endpoints.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date October 30, 2022
Est. primary completion date October 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Scheduled thoracic resection Surgery for lung- or esophagus cancer. For lung cancer patients, at least one lung lobe has to scheduled for resection Exclusion Criteria: - Known Diaphragmatic Dysfunction - Neuromuscular Disease - Pleural Effusion > 1cm - Pneumothorax - Known Phrenic Nerve Palsy

Study Design


Intervention

Procedure:
Lung lobectomy OR esophagus cancer resection
Lunge lobectomy (total) Resection of esophagus cancer

Locations

Country Name City State
Denmark Department of Anaesthesiology and Intensive Care East Section, Aarhus University Hospital Aarhus N

Sponsors (1)

Lead Sponsor Collaborator
Aarhus University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in excursion of the diaphragm Ultrasonographic measure with M-mode of Diaphragmatic Excursion on right hemidiaphragm Prior to surgery to 14 days after surgery
Secondary Ultrasonographic measure of the difference in Intrathoracic Area Intrathoracic Area is measured at inspiration and expiration to calculate the difference in Intrathoracic Area during breathing Prior to surgery to 14 days after surgery
Secondary Change in Diaphragmatic Thickening Fraction Ultrasonographic measurement Prior to surgery to 14 days after surgery
Secondary Change in Intercostal Muscle Thickening Fraction Ultrasonographic measurement Prior to surgery to 14 days after surgery
Secondary Change in forced expired volume within the first second (FEV1) Spirometry Prior to surgery to 14 days after surgery
Secondary Change in forced vital capacity (FEV) Spirometry Prior to surgery to 14 days after surgery
Secondary Change in peak flow Spirometry Prior to surgery to 14 days after surgery
Secondary Change in Electromyographic measure of Maximal Diaphragmatic Response after stimulating the phrenic nerve Prior to surgery to 14 days after surgery
Secondary Change in Electromyographic measure of Latency of Diaphragmatic Response after stimulating the phrenic nerve Prior to surgery to 14 days after surgery
Secondary Change in 6 Minutes Walk Test Maximum Walking Distance within 6 minutes Prior to surgery to 14 days after surgery
Secondary Change in visual analogue scale score Scoring system for subjective sensation of pain ranging from 0 to 10. Higher numbers signify higher pain sensations Prior to surgery to 14 days after surgery
Secondary Accumulated Opiod Use after Surgery Morphine equivalents Prior to surgery to 14 days after surgery
Secondary Postoperative Pulmonary Complications Comprising:
Pneumonia
Atelectasis
Bronchospasm
Hypoxemia
Severe Hypoxemia
Pleural Effusion 1 > cm
Pneumothorax
CPAP or NIV required after 1. postoperative day
Prior to surgery to 30 days after surgery
Secondary Admission days at the Intensive Care Unit after Surgery Prior to surgery to 60 days after surgery
Secondary Number of Admissions after Discharge from the Surgical Department Prior to surgery to 60 days after surgery
Secondary Accumulated Admission Days at any Hospital Prior to surgery to 60 days after surgery
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