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OpenTrials
Active, Not Recruiting

NCT Number: NCT03567538

National Register Studies in Thoracic Surgery

The overall project aim is to study risk and outcomes following thoracic surgery by cross-linking high-quality national Swedish health-data registers for population-based investigations of individual level clinically relevant patient data.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

18 year–110 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Karolinska University Hospital

Stockholm, 171 76, Sweden

About this study

The purpose of this research project is to study risks and outcomes in patients who underwent thoracic surgery, primarily for lung cancer. We aim to establish a fundament for the conduct of nationwide population-based studies by linking patient-level data from the Swedish quality register for thoracic surgery (ThoR) and other national health-data registers maintained by the government agencies Statistics Sweden and the National Board of Health and Welfare. Cross-linking patient-level data is possible through the Personal Identity Number assigned to every individual who has resided in Sweden on a permanent basis. The Swedish Personal Identity Number is the unique identifier in all national registers.

Specifically, we aim:

  • To analyze the association between socioeconomic factors and prognosis in patients undergoing pulmonary resection for lung cancer.
  • To investigate the implementation of minimally invasive surgery for lung cancer in Sweden.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

All adult patients who underwent thoracic surgery in Sweden during the study period

Exclusion criteria

-

Treatment and study plan

thoracic surgery

Procedure

Thoracic surgery, pulmonary resection, minimally invasive thoracic surgery, video assisted thoracic surgery (VATS)

Primary outcomes

  1. All-cause mortality

    Time frame: 15 years

    Death from any cause

Secondary outcomes

  1. Postoperative complications

    Time frame: 30 days

    Complications related to surgery

Sponsors and collaborators

Lead sponsor

Karolinska University Hospital

Other

Collaborators

  • Karolinska Institutet

Registry information

Important dates

Study start
2018
Primary completion
2026
Study completion
2026
First posted
Jun 25, 2018
Registry last updated
Oct 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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