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NCT07291180 · ClinicalTrials.gov registry record · NA

A Feasibility Study of Mass-Based Response Drug Screening to Guide Personalized Hyperthermic Intraperitoneal Chemotherapy for High-Grade Appendiceal and Colorectal Adenocarcinoma With Peritoneal Metastasis

A NA study of Colorectal Adenocarcinoma and Appendiceal Cancer, sponsored by Yale University.

Recruiting
Registry status
NA
Development phase
20
Enrollment target
1
Study location

NCT07291180: Recruiting NA study of Colorectal Adenocarcinoma and Appendiceal Cancer, sponsored by Yale University.

NCT07291180 is a NA study of Colorectal Adenocarcinoma and Appendiceal Cancer that is actively recruiting participants, run by Yale University. The registered enrollment target is 20 participants, below the 318-participant average among 19 other Colorectal Adenocarcinoma trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07291180, a NA study of Colorectal Adenocarcinoma and Appendiceal Cancer, is actively recruiting participants, sponsored by Yale University.

RECRUITING
Registry status
NA
Development phase
20 participants
Enrollment target
1
Study location

Study Summary

This study will evaluate the role of mass-based response testing (MRT) to select and deliver personalized hyperthermic intraperitoneal chemotherapy (HIPEC) regimens to patients with peritoneal metastasis (PM) from high-grade appendiceal adenocarcinomas (HGAA) and colorectal cancer (CRC).

Primary Outcome

Feasibility is defined as the percentage of treatment naïve and pretreated patients who successfully receive drug screening results within one week of tissue sampling from at least one peritoneal biopsy. This means that the test has enough tumor cell viability and purity to come back with specific results indicating sensitivities of HIPEC drugs and does not give an inconclusive result (due to insufficient tissue sample).

Interventions

  • DEVICE Mass-based response testing (MRT)

Study Locations (1)

Connecticut

  • Yale New Haven Hospital - New Haven

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2026-03
Est. Completion 2027-12
Phase NA
Yale University

1,492 total trials

What NCT07291180 shows while recruiting

NCT07291180 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 318-participant average among 19 other Colorectal Adenocarcinoma trials with a reported enrollment target (94% lower).

The record links to 3 conditions, with Colorectal Adenocarcinoma appearing as the primary indexed condition, and to 1 intervention - of which Mass-based response testing (MRT) is the first listed.

NCT07291180 reports a single indexed study location in Connecticut.

Frequently Asked Questions

What is clinical trial NCT07291180 about?

NCT07291180 is a clinical study titled "A Feasibility Study of Mass-Based Response Drug Screening to Guide Personalized Hyperthermic Intraperitoneal Chemotherapy for High-Grade Appendiceal and Colorectal Adenocarcinoma With Peritoneal Metastasis". This study will evaluate the role of mass-based response testing (MRT) to select and deliver personalized hyperthermic intraperitoneal chemotherapy (HIPEC) regimens to patients with peritoneal metastasis (PM) from high-grade appendiceal adenocarcinomas (HGAA) and colorectal cancer (CRC).

What is the current status of trial NCT07291180?

This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2026-03. Estimated completion is 2027-12.

What conditions does trial NCT07291180 study?

This clinical trial studies the following conditions: Colorectal Adenocarcinoma, Appendiceal Cancer, Peritoneal Metastases.

What interventions are being tested in trial NCT07291180?

The interventions under investigation include: Mass-based response testing (MRT) (DEVICE).

Who is sponsoring clinical trial NCT07291180?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07291180 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Colorectal Adenocarcinoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07291180's enrollment target sits among peer trials

20 18th of 19 higher than 2 of 19 other Colorectal Adenocarcinoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Colorectal Adenocarcinoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07291180, the US trial registry maintained by the National Library of Medicine. NCT07291180 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.