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Recruiting NCT04644952

The Rise in Robotic Atypical Segmentectomies

Observational Lung Carcinoma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Electronic Health Record Review.
Who it may be relevant to
Registry conditions: Lung Carcinoma. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Rise in Robotic Atypical Segmentectomies: A Large Cancer Center Experience

Overview

This study investigates the increased rate of robotic atypical segmentectomies. Segmentectomy refers to removing a section of a lobe of the lung. Reviewing patients' data retrospectively may help researchers determine whether robotic surgery has led to an increase in atypical segmentectomy.

Detailed description

PRIMARY OBJECTIVES:

I. To evaluate the rate of increase in robotic segmentectomies performed at our institution per year.

II. To evaluate the rate of typical and atypical segmentectomies performed at our institution per year.

III. To characterize the differences in robotic versus other types of resections such as open and VATS (video-assisted thoracic surgery).

OUTLINE:

Patients' medical records are reviewed retrospectively.

Interventions

  • Other Electronic Health Record Review
    Review of medical records

Primary outcome measures

  • Rate of change in robotic segmentectomies [Time frame: Up to 2 years]
  • Rate of typical and atypical segmentectomies [Time frame: Up to 2 years]
  • Differences in robotic versus other types of resections such as open and video-assisted thoracic surgery [Time frame: Up to 2 years]

Eligibility criteria

Inclusion criteria

  • Patients who underwent a lung resection from 2004 to 2019

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

United States · 1 center
  • M D Anderson Cancer Center — Houston

Identifiers

NCT: NCT04644952 · 2020-0696 · NCI-2020-10080 · 2020-0696

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗