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Trial Title:
Predictors of Acute and Persistent Postoperative Pain in Lung Cancer Surgery
NCT ID:
NCT05599386
Condition:
Lung Cancer
Conditions: Official terms:
Lung Neoplasms
Pain, Postoperative
Study type:
Observational
Overall status:
Active, not recruiting
Study design:
Time perspective:
Prospective
Intervention:
Intervention type:
Diagnostic Test
Intervention name:
Preoperative test
Description:
Patients are subject to quantitative sensory testing, questionnaires, and biomarker
analysis prior to surgery.
Arm group label:
Patients Undergoing VATS
Summary:
The aim of this observational study is to investigate if preoperative quantitative
sensory testing, anxiety and depression symptoms, and biological markers are associated
with the risk of developing acute and chronic postoperative pain after video-assisted
Thoracoscopic surgery (VATS).
Detailed description:
This observational study examine acute and chronic postoperative pain in patients
undergoing VATS. In the study preoperative biomarkers, quantitative sensory testing and
questionnaires are used to create prediction models for acute and chronic postoperative
pain. The study will serve as background information on the risk factors and predictive
factors as well as an exploration of the impact of surgical stress from VATS on
circulation microRNA and inflammatory mediators.
Criteria for eligibility:
Study pop:
Public University hospital
Sampling method:
Probability Sample
Criteria:
Inclusion Criteria:
- Adults independent of sex with an age of ≥ 18 years
- Patients scheduled for VATS as a part of either examination or radical treatment of
lung cancer
Exclusion Criteria:
- Patients who are unable to understand oral and written information.
- Patients with known chronic pain in the thorax which have been persisting for at
least six months before the day of surgery.
- Pregnant and nursing women.
- Patients receiving a planned preoperative epidural blockade during their stay.
- Patients converted to open surgery.
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Aalborg University Hospital
Address:
City:
Aalborg
Zip:
9000
Country:
Denmark
Start date:
November 1, 2022
Completion date:
August 6, 2024
Lead sponsor:
Agency:
Jannie Bisgaard Stæhr
Agency class:
Other
Collaborator:
Agency:
Aalborg University
Agency class:
Other
Source:
Aalborg University Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05599386