NCT04212481|Unknown
RCT of Uniport VATS for Lung Cancer
Randomized Controlled Trial of the Comparison of Uniport VATS and Non- Uniport VATS for Lung Cancer
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Randomized Controlled Trial of the Comparison of Uniport VATS and Non- Uniport VATS for Lung Cancer
Sponsor study identifier
interventional
300
1 country
1
Study Start
December 25, 2019
Actual (reported)Primary Completion
December 30, 2022
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
December 30, 2025
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Video-assisted thoracoscopic surgery (VATS) has been widely used for non-small cell lung cancer (NSCLC) for nearly two decades. Usually, it was applied through three ports with at least one drainage after surgery, which often lead to acute chest pain. Therefore, fewer, smaller ports, and wider intercostal space for surgery has been required. Uniport VATS became a feasible option with the development of surgical techniques and instruments, with potentially less postoperative pain and shorter hospital stays. However, there may be some complications, or with a longer time of operation, even more difficult in lymph nodes resection during learning curve. In our study, a Randomized Controlled Trial was designed to study the operation time, perioperative blood loss, conversion rate, duration of postoperative drainage, length of hospital stay, visual analogue score of postoperative pain, complications, and survival.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
December 30, 2025
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
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Some registry-reported names shown below are not yet linked in this graph.
Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
December 21, 2019
Actual (reported)December 25, 2019
Actual (reported)December 27, 2019
Actual (reported)December 30, 2022
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
December 30, 2025
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
operative time
operative time in minutes
1 day
perioperative blood loss
perioperative blood loss in milliliter
1 day
conversion rate
conversion rate in proportion
1 day
duration of postoperative drainage
duration of postoperative drainage in days
within 5-7 days
length of hospital stay
length of hospital stay in days
within 5-7 days
visual analogue score of postoperative pain
score
within 5-7 days
overall survival
up to 5 years
progression- free survival
up to 5 years
Uniport video-assisted thoracoscopic surgery for NSCLC
video-assisted thoracoscopic surgery for NSCLC using two ports
video-assisted thoracoscopic surgery for NSCLC using three ports
video-assisted thoracoscopic surgery for NSCLC using single port or two ports or three ports
video-assisted thoracoscopic surgery for NSCLC using two ports
The Second Hospital of Shandong University
Jinan, Shandong, 250033, China
Xiaogang Zhao, Doctor
The Second Hospital of Shandong University
First Submitted
December 21, 2019
First Posted
December 27, 2019
Study Start
December 25, 2019
Actual (reported)Primary Completion
December 30, 2022
Estimated (date passed)complications
complications in rate
up to 3 months
video-assisted thoracoscopic surgery for NSCLC using three ports
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This estimate has passed. The registry has not confirmed an actual date for this milestone.
Study Completion
December 30, 2025
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Last Updated
November 16, 2022
Record last verified: 2022-11
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Source: ClinicalTrials.gov.
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