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Completed No phase listed Observational

SafeHeal Diverting Ileostomy Pivotal Study

ClinicalTrials.gov ID: NCT06152276

Public ClinicalTrials.gov record NCT06152276. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 3:47 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

SafeHeal Diverting Ileostomy Pivotal Study (SH-SOC23)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This SafeHeal study is designed to assess the overall safety of the low anterior resection (LAR) standard of care cancer treatment by establishing a definition of major complications. The current literature on standard of care reports adverse events/complications but does not provide a single endpoint that can be used to compare the safety of LAR cancer treatment to alternative therapies or treatments. This study will allow for the establishment of a new single safety endpoint for LAR standard of care cancer treatment.

Study identification

NCT ID
NCT06152276
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
SafeHeal Inc
Industry
Enrollment
132 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 1, 2024 (Actual)
Primary completion
Jan 30, 2026 (Actual)
Completion
Jan 30, 2026 (Actual)
Last update posted
May 4, 2026

2024 – 2026

United States locations

U.S. sites
15
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
Kaiser Permanente - Los Angeles Los Angeles California 90027 —
Keck Medicine of USC Los Angeles California 90033 —
USC Keck Hospital Los Angeles California 90033 —
Cedars-Sinai Medical Center Los Angeles California 90048 —
University of Miami Miami Florida 33146 —
Tampa General Hospital Tampa Florida 33606 —
Northwestern University Chicago Illinois 60611 —
Boston Medical Center Boston Massachusetts 02118 —
UMass Memorial Medical Center Worcester Massachusetts 01605 —
Maimonides Medical Center Brooklyn New York 11219 —
Mount Sinai Hospital New York New York 10029 —
New York Presbyterian Cornell New York New York 10065 —
Lenox Hill Hospital New York New York 10075 —
Novant Health Winston-Salem North Carolina 27103 —
Lankenau Medical Center Wynnewood Pennsylvania 19096 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06152276, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 4, 2026 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06152276 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →