NCT06506331Completed
Impact of Preoperative VFA on Intraoperative Adverse Events in Patients Undergoing Laparoscopic Radical Gastrectomy
Impact of Preoperative Visceral Fat Area on Intraoperative Adverse Events in Patients Undergoing Laparoscopic Radical Gastrectomy: A Pooled Analysis From Two Randomized Trials
Source: ClinicalTrials.gov · Last updated 17 Jul 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
Preoperative visceral fat area (VFA) is associated with an increased incidence of postoperative complications in gastric cancer (GC). However, the relationship between VFA and intraoperative adverse events (iAEs) remains unclear. Therefore, this study aimed to evaluate the impact of preoperative VFA on iAEs in patients undergoing laparoscopic radical gastrectomy for GC, using data from two prospective trials. Simultaneously, a predictive model for iAEs was constructed to provide a basis for the early identification of high-risk populations and the implementation of personalized perioperative management measures.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 490 (actual)
- First submitted
- 11 Jul 2024
- Start date
- 1 Dec 2012
- Primary completion date
- 1 Apr 2016
- Lead sponsor
- Fujian Medical University
- NCT number
- NCT06506331
What you commit to
- Study type: Observational
- Participants enrolled: 490
- From 1 Dec 2012 to the primary completion date, 1 Apr 2016
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- open surgery;
- Palliative surgery
Other illness
- non-adenocarcinoma gastric cancers
Other
- Exploratory operation
- CT data missing
Who the study is looking for
- This study comprised two prospective trials conducted at Fujian Medical University Union Hospital (FMUUH): the FUGES-001 study (ClinicalTrials.gov, NCT02327481) and a subset of the CLASS-01 multicenter study (ClinicalTrials.gov, NCT01609309)
Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.