Stomach Cancer Trial, Recruiting NCT03716089 Sponsor: Fujian Medical University Condition: Stomach Cancer
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Stomach Cancer Trial, Recruiting

NCT03716089
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People aged between 18 and 75 years old
  • People who have been diagnosed with a stomach tumour called a GIST (a type of gastrointestinal stromal tumour), confirmed by a tissue sample taken during a scope procedure, or confirmed after surgery
  • People who have provided written agreement to take part in the trial
  • People whose tumour is expected to be fully removed by keyhole (laparoscopic) surgery, with no cancer left behind
  • People who are generally well enough to carry out light activity, as measured by a standard health scale (ECOG score of 0 or 1)
  • People considered to be at low to moderate risk for anaesthesia, as assessed by a standard medical rating (ASA class I to III)
  • People whose tumour measures 10 centimetres or less at its widest point

Who may not be able to join:

  • People who are pregnant or breastfeeding
  • People who have a serious mental health condition
  • People who have had previous surgery on the upper abdomen, except for keyhole gallbladder removal
  • People who have had previous surgery on the stomach, including certain endoscopic procedures for stomach cancer
  • People who do not wish to have keyhole surgery
  • People who have had another cancer diagnosis within the past five years
  • People who have had unstable chest pain (angina) or a heart attack in the past six months
  • People who have had a stroke or related brain blood vessel event in the past six months
  • People who have been taking corticosteroid medications regularly for at least one month leading up to the trial
  • People who need another surgical procedure performed at the same time
  • People who require emergency surgery due to serious complications such as bleeding, blockage, or a hole in the stomach
  • People whose lung breathing capacity (FEV1) is below 50% of the normal expected level (confirm with trial site)
  • People whose tumour measures more than 10 centimetres at its widest point

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Fujian Medical University
Registry
ClinicalTrials.gov
Start date
11 October 2018
Est. completion
1 April 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

3-year disease free survival rate

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov