Fact CheckerSign in

NCT06597526Recruiting

The Role of 18F-FDG&68Ga-FAPI PET/CT in the Assessment of Conversion Therapy Efficacy in Gastric Cancer with Peritoneal Metastasis.

The Role of 18F-FDG & 68Ga-FAPI PET/CT in the Assessment of Conversion Therapy Efficacy in Gastric Cancer with Peritoneal Metastatic

Source: ClinicalTrials.gov · Last updated 19 Sept 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study aims to investigate the value of 18F-FDG\&68Ga-FAPI PET/CT in evaluating the outcome of conversion therapy and the prognosis of people with peritoneal metastases from gastric cancer.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
10 Sept 2024
Start date
15 Jun 2024
Primary completion date
31 Mar 2028
Lead sponsor
Ruijin Hospital
NCT number
NCT06597526

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 15 Jun 2024 to the primary completion date, 31 Mar 2028
  • 1 site in 1 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.

Other illness

  • Patients with a history of other malignant diseases in the last 5 years, except cured skin cancer and carcinoma in situ of cervix
  • Severe mental disease, uncontrolled epilepsy, or central nervous system disease

Other

  • Signs of distant metastases other than peritoneal metastases at enrolment
  • Pregnant or breastfeeding women.

Who the study is looking for

  • Histologically confirmed gastric adenocarcinoma with no history of resection of primary or metastatic lesions
  • Peritoneal metastases of gastric cancer requiring laparoscopy for definitive diagnosis without gastric outflow tract obstruction and intestinal obstruction
  • Patients voluntarily enrolled in this study by signing an informed consent form
  • Age ≥ 18 years
  • Eastern Cooperative Oncology Group (ECOG) score ≤ 2,
  • Expected life expectancy ≥ 3 months
  • Adequate organ and bone marrow function
  • Willingness to adhere to the study protocol and follow-up programme

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ruijin Hospital affiliated to Shanghai Jiao Tong University of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.