Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05879159

Accelerated Recovery After MIS Hepatectomy (ARAMIS Hep) to Support Early Discharge for Patients Undergoing Minimally Invasive Liver Resection

Led by M.D. Anderson Cancer Center · Updated on 2026-04-15

36

Participants Needed

1

Research Sites

173 weeks

Total Duration

On this page

Sponsors

M

M.D. Anderson Cancer Center

Lead Sponsor

I

Intuitive Surgical

Collaborating Sponsor

AI-Summary

What this Trial Is About

To learn if an accelerated recovery program can shorten the length of hospital stay in patients having minimally invasive liver surgery.

CONDITIONS

Official Title

Accelerated Recovery After MIS Hepatectomy (ARAMIS Hep) to Support Early Discharge for Patients Undergoing Minimally Invasive Liver Resection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Tumor suitable for minimally invasive Kawaguchi-Gayet grade I hepatectomy
  • No evidence of cirrhosis based on imaging, clinical features, or lab results
  • No significant cardiopulmonary disease preventing minimally invasive surgery
  • Ability to stay within 50 miles of the medical center during the immediate postoperative period
  • Age 18 years or older
  • Ability to understand and sign informed consent
  • Non-English-speaking patients are eligible
Not Eligible

You will not qualify if you...

  • Tumors not suitable for minimally invasive Kawaguchi-Gayet grade I hepatectomy
  • Tumors not suitable for minimally invasive or robotic-assisted surgery
  • Evidence of cirrhosis on imaging, clinical exam, or labs
  • Inability to stay within 50 miles of the medical center immediately after surgery
  • Age below 18 years
  • Inability to provide informed consent
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

H

Hop Tran Cao, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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