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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

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