ClinicalTrials.Veeva

Menu

Peritoneal Lavage for Early Detecting Gene Mutation of Peritoneal Metastasis of Gastric Cancer

Fudan University logo

Fudan University

Status

Completed

Conditions

Gastric Cancer

Treatments

Other: Observational study

Study type

Observational

Funder types

Other

Identifiers

NCT03314649
CGCG003

Details and patient eligibility

About

Our study aims to improve sensitivity and accuracy of detecting abdominal free cancer cells in patients with gastric cancer.

Full description

Gastric cancer (GC) remains one of the most common causes of cancer-related mortality worldwide. Surgery has always been considered as the most effective treatment for GC. Peritoneal metastasis is the common pattern of postoperative recurrence, especially patients with T4 stage or serosal invasion. What is worse, patients with peritoneal metastasis have a poor prognosis. However, it is often difficult to diagnose peritoneal metastasis at an early stage. As we know, the implantation of peritoneal free cancer cells exfoliating from serosa-invasive tumors is main reason of peritoneal seeding. Cytological examination of peritoneal lavage fluid is always performed to predict peritoneal micrometastases. However, more than half of patients with negative cytological results develop peritoneal recurrence. Low sensitivity and poor negative predictive value of this method have heralded the development of advanced techniques in detecting peritoneal free cancer cells.

In this study, novel genetic techniques will be used to detect mutated DNA of shed cancer cells in abdominal cavity. The present clinical trial aims to find a better tool to detect abdominal micrometastasis in GC patients, which may become a valid clinical index to predict postoperative relapse and direct treatment.

Enrollment

200 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Lower age limit of research subjects 18 years old and upper age limit of 80 years old.
  2. PS (ECOG) of 0 or 1 and expected to survive more than 6 months.
  3. Written informed consent from the patient.
  4. Patients suffering gastric cancer and non-cancerous disease planned to have laparotomy.

Exclusion criteria

  1. Female in pregnancy or lactation. 2. Patients participating in any other clinical trials currently,or participated in other trails within 1 months. 3. Patients with poor compliance or considered to be poor compliance.

Trial design

200 participants in 1 patient group

Observational study
Description:
Patients with gastric cancer and non-cancerous disease planned to have laparotomy
Treatment:
Other: Observational study

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems