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Trials / Recruiting

RecruitingNCT04107077

Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

A Phase IIa Study of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) and PD-L1 Expression in Gastric Cancer With Peritoneal Metastases

Status
Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
21 (estimated)
Sponsor
University of Chicago · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

To assess if PD-L1 expression can be upregulated in peritoneal metastases from gastric cancer after the administration of HIPEC with greater frequency compared to systemic chemotherapy alone

Conditions

Interventions

TypeNameDescription
DRUGCisplatinLaparoscopic HIPEC will be performed at a maximum of two (2) times spaced approximately 6 weeks apart. The dosing of the drugs will be the same during each administration but adjusted if needed based on lab work. The typical dosages are 200mg of Cisplatin
DRUGMitomycinLaparoscopic HIPEC will be performed at a maximum of two (2) times spaced approximately 6 weeks apart. The dosing of the drugs will be the same during each administration but adjusted if needed based on lab work. The typical dosages are 30mg of Mitomycin C.

Timeline

Start date
2025-09-09
Primary completion
2026-06-01
Completion
2026-06-01
First posted
2019-09-27
Last updated
2025-10-07

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04107077. Inclusion in this directory is not an endorsement.