Perioperative Management and Outcomes of Minimally Invasive Esophagectomy
1 other identifier
observational
64
1 country
1
Brief Summary
The investigators retrospectively reviewed the data of all patients who had undergone esophagectomy and reconstruction in 2015. Patient characteristics, the surgery performed, method of anesthesia, postoperative hospitalization course, and additional surgical interventions were reviewed and analyzed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jun 2017
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
September 15, 2017
CompletedFirst Submitted
Initial submission to the registry
December 15, 2017
CompletedFirst Posted
Study publicly available on registry
December 20, 2017
CompletedDecember 20, 2017
December 1, 2017
2 months
December 15, 2017
December 19, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
30-day mortality
rate of 30-day mortality
30 day after surgery
Interventions
all the included participants had received esophagectomy, either Ivor Lewis or tri-incision, or more complex procedures.
Eligibility Criteria
patients with esophageal cancer undergoing esophageal reconstruction in 2015.
You may qualify if:
- patients received esophageal reconstruction in 2015.
You may not qualify if:
- age \<18
- not malignancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
NTUH
Taipei, Taiwan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Ya-Jung Cheng, MD. PHD
Chief of Department of Anesthesiology, National Taiwan University Hospital
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 15, 2017
First Posted
December 20, 2017
Study Start
June 1, 2017
Primary Completion
August 1, 2017
Study Completion
September 15, 2017
Last Updated
December 20, 2017
Record last verified: 2017-12
Data Sharing
- IPD Sharing
- Will not share