The Effects of Gastric Tube on the Quality of Life and Nutritional Status After Ivor-Lewis Esophagectomy
NCT ID: NCT01361750
Last Updated: 2020-03-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
TERMINATED
NA
21 participants
INTERVENTIONAL
2011-05-31
2012-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Impact on Quality of Life in Patients Undergoing Total Gastrectomy or Proximal Gastrectomy for Adenocarcinoma of Esophagogastric Junction
NCT01697917
Gastrointestinal Functional Outcome Ivor Lewis
NCT03658837
Conventional Oral Intake vs Delayed Oral Intake With Jejunostomy Feeding After Esophagectomy (JNS Study)
NCT05318404
Functional Jejunal Interposition Improve Nutritional Status After Total Gastrectomy
NCT01996059
Goal-directed Enteral Nutritional Perioperative Management
NCT06510543
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
gastirc tube group
conduit will be perfomed by narrowed gastric tube
gastric tube
the stomach will be cut into a narrowed tube-shape conduit
control group
conduit will be traditional subtotal stomach without any surgical modification
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
gastric tube
the stomach will be cut into a narrowed tube-shape conduit
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* eligble for Ivor-Lowis esophagectomy
* expected survival time longer than 12 months
Exclusion Criteria
* anastomosis leak
* jejunum or colon transversum interponate
30 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Peking University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yang Yue
Thoracic Surgery II
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Yue Yang, M.D.
Role: PRINCIPAL_INVESTIGATOR
Peking University Health Science Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Peking University School of Oncology
Beijing, Beijing Municipality, China
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PKU-OES-001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.