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NCT04840264RecruitingPhase 2

Docetaxel, Oxaliplatin and 5-FU for Gastric Cancer With Inoperable Malignant Bowel Obstruction

A Multi-center, Non-randomized, Three-cohort, Phase II Trial of a Modified Triplet Combination of Docetaxel, Oxaliplatin and Fluorouracil for Gastric Cancer With Peritoneal Carcinomatosis and Inoperable Malignant Bowel Obstruction

Source: ClinicalTrials.gov · Last updated 13 Jul 2026

Brief summary (registry, in English)

This is a multi-center, non-randomized, 3-cohort, phase II trial, evaluating a triplet combination of docetaxel, oxaliplatin and fluorouracil for gastric cancer with peritoneal carcinomatosis and inoperable malignant bowel obstruction.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
79 (estimated)
First submitted
11 Sept 2019
Start date
7 Jan 2022
Primary completion date
31 Dec 2027
Lead sponsor
Sixth Affiliated Hospital, Sun Yat-sen University
NCT number
NCT04840264

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 79
  • From 7 Jan 2022 to the primary completion date, 31 Dec 2027
  • 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.

Prior treatment

  • treated by a combination regimen containing all the study drugs;
  • concomitant cerebral parenchymal or meningeal metastasis;
  • bowel surgery or stenting required due to obstruction;

Other illness

  • allergy to any of the study drugs;
  • active gastrointestinal bleeding;
  • uncontrolled active infection;
  • unstable heart diseases with severe ECG abnormalities or affect clinical treatment (such as cardiac insufficiency, myocardial infarction, angina);
  • severe lung diseases (such as interstitial pneumonia, pulmonary fibrosis, severe emphysema, etc);
  • mental disorders that affect clinical treatment or central nervous system diseases;
  • HIV infection or untreated active hepatitis;
  • other conditions that are not suitable for participation in the study.

Other

  • HER-2 amplification or overexpression, mismatch repair protein expression deletion (dMMR), or genetic testing suggestive of high microsatellite instability (MSI-H);
  • strangulated intestinal obstruction;
  • pregnant or lactating women;

Who the study is looking for

  • 18-75 years of age;
  • ECOG PS ≤3;
  • pathologically diagnosed gastric or gastroesophageal junctional adenocarcinoma;
  • peritoneal carcinomatosis established by imaging data or pathological evidence;
  • MBO below the Treitz ligament based on clinical grounds or radiological findings;
  • considered as inoperable MBO by two independent surgical consultants;
  • Hb≥60g/L, WBC ≥4×10E9/L, ANC≥2×10E9/L,PLT≥100×10E9/L;
  • Cr≤ Upper Normal Limit(UNL);
  • Tbil≤1.5 UNL,AST≤1.5 UNL, ALT≤1.5 UNL, ALP≤1.5 UNL;
  • Written informed consent form paticipants.

Age in the registry: 18 years to 75 years · 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
Guangdong Provincial People's Hospital
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

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