Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07211386

The Erector Spinae Plane Block For Gastrointestinal Malignancy Pain Treatment (EGIPT)

Led by Abramson Cancer Center at Penn Medicine · Updated on 2025-11-28

25

Participants Needed

4

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will target patients with gastrointestinal (GI) malignancy who present to any of 4 Penn Medicine emergency departments (EDs) with intractable abdominal pain. We will offer eligible patients an erector spinae plane block (ESPB), a regional anesthesia technique which is already offered to such patients in the ED at the University of Pennsylvania Healthy System (UPHS), for their intractable abdominal pain. We will compare the outcomes of this prospective cohort of patients to a matched historical control of patients with GI malignancy who were treated in the ED during the same time period as recruitment, but who were not recruited to partake in the study and who were managed with standard of care. Opioid consumption as measured by total milligram morphine equivalents (MMEs) over a 24-hour period and hospital length of stay (LOS) will be compared between cohorts. Additionally, for the ESPB cohort, pain level pre/post ESPB, and functionality and satisfaction with pain management at 24 hours will also be examined.

CONDITIONS

Official Title

The Erector Spinae Plane Block For Gastrointestinal Malignancy Pain Treatment (EGIPT)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients age > 18 years old with GI malignancy presenting to a Penn Medicine emergency department with intractable abdominal pain
  • Same-day or recent CT scan of the abdomen or pelvis showing that abdominal pain is likely due to a malignant source
Not Eligible

You will not qualify if you...

  • Allergy to ropivacaine or history of local anesthetic systemic toxicity
  • Pregnancy
  • Incarcerated status
  • Admission for serial abdominal examinations to determine surgical course
  • Altered mental status or inability to consent for the procedure
  • Hemodynamic instability
  • Previously enrolled in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 4 locations

1

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

2

Penn Presbyterian Medical Center

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

3

Pennsylvania Hospital

Philadelphia, Pennsylvania, United States, 19107

Actively Recruiting

4

Hospital of the University of Pennsylvania -- Cedar Avenue

Philadelphia, Pennsylvania, United States, 19143

Actively Recruiting

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Research Team

U

Umar Aulia, AB

CONTACT

M

Michael Shalaby, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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