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NCT07313579Recruiting

Hyperthermic Intraperitoneal Chemoperfusion (HIPEC) in Gastric Cancer

Observational Prospective Cohort Study on Hyperthermic Intraperitoneal Chemoperfusion (HIPEC) in Gastric Cancer

Source: ClinicalTrials.gov · Last updated 13 Jan 2026

Brief summary (registry, in English)

The study investigates the outcomes of hyperthermic intraperitoneal chemoperfusion (HIPEC) in combination with curative-intent gastrectomy in resectable locally-advanced and limited-metastatic (low peritoneal cancer index) gastric cancer.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
8 Dec 2025
Start date
1 Dec 2025
Primary completion date
1 Dec 2030
Lead sponsor
Ukrainian Society of Clinical Oncology
NCT number
NCT07313579

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 1 Dec 2025 to the primary completion date, 1 Dec 2030
  • 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

  • Concomitant malignancy

Other illness

  • Mitomycin and/or Cisplatin hypersensitivity
  • Uncontrollable chronic diseases
  • Patients with coexisting malignancy other than basal cell carcinoma of the skin within the last five years.
  • History of allergic reactions associated with cisplatin and Mitomycin C
  • Patients with psychiatric illness/social situations with impaired compliance

Other

  • Pregnancy/breastfeeding
  • ECOG status 2-4
  • Presence of metastases other than regional or peritoneal (such as liver, lungs, bone, brain, distant lymph nodes)
  • •Refusal to participate

Who the study is looking for

  • Age 18-80
  • Hystologicaly proven gastric adenocarcinoma
  • ECOG status 0-1
  • Written consent to participate in the study
  • Medically and technically operable gastric tumor
  • Only T4a or T4b tumours with any peritoneal cytology status
  • Cytologically positive peritoneal washings (cyt+) with any T and N criteria
  • Adequate haemopoetic, renal and hepatic function (Hb \> 120, PLT \> 150\*10\^9/l, ALT \< 60, AST \<40, total bilirubin \< 21 µmol/l, Creatinine clearance (male - 90-140, female - 80-130 ml/min)

Age in the registry: 18 years to 80 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
National Cancer Institute (NCI)
Coordinator of this site? Confirm its status
KyivUkraineRecruiting

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