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OncoMatch/Clinical Trials/NCT07282834

Heated Versus Aerosol-based Laparoscopic Chemotherapy for Cancer That Has Spread to the Peritoneum (Abdominal Lining)

Is NCT07282834 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies non-drug interventions for peritoneal (metastatic) cancer.

Phase 2RecruitingPatrick Wagner, MD, FACSNCT07282834Data as of May 2026

This research study aims to improve the treatment of Peritoneal Carcinomatosis (PC), a condition where cancer spreads within the abdomen. Patients with PC often experience significant pain and nutritional problems. Currently, there isn't a standard treatment approach, and doctors use different combinations of chemotherapy, surgery, and methods to deliver chemotherapy directly into the abdomen (intra-peritoneal or "IP" chemotherapy). The study will compare two IP chemotherapy methods: HIPEC and PIPAC. HIPEC involves circulating heated chemotherapy through the abdomen during surgery, while PIPAC delivers chemotherapy as a pressurized aerosol during a laparoscopic procedure. Both methods aim to achieve the same goal, but they haven't been directly compared to see which is safer, more tolerable, more effective, and provides better value.

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Extracted eligibility criteria

Cancer type

Ovarian Cancer

Disease stage

Metastatic disease required

Prior therapy

Must have received: systemic chemotherapy

Receipt of at least three months of standard systemic chemotherapy prior with persistence of disease at the time of randomization

Cannot have received: investigational drug

Any investigational drug use within 30 days prior to enrollment

Cannot have received: systemic therapy

Systemic therapy within 14 days prior to randomization

Lab requirements

Blood counts

Hemoglobin < 7 gm/dL, WBC < 3,000/mm3, Platelet count < 50,000/mm3 (exclusion)

Kidney function

clinically significant renal disease (exclusion)

Liver function

AST/SGOT > 2.5x ULN, ALT/SGPT > 2.5x ULN, Total bilirubin > 2.5x ULN (exclusion)

Laboratory abnormalities that indicate clinically significant hematologic, hepatobiliary, or renal disease: AST/SGOT > 2.5x ULN, ALT/SGPT > 2.5x ULN, Total bilirubin > 2.5x ULN, Hemoglobin < 7 gm/dL, White blood cell count < 3,000/ mm3, Platelet count < 50,000/mm3

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Allegheny Health Network West Penn Hospital · Pittsburgh, Pennsylvania

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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