Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID03862781

Randomized Trial of Intra-Corporeal Anastomosis for Right Colectomies (RICART Study)

Led by Corewell Health West · Updated on 2026-01-21

125

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to evaluate whether minimally invasive right hemicolectomies performed with an intra-corporeal anastomosis lead to a quicker return of bowel function and earlier hospital discharge. The study focuses on adult patients scheduled for this surgery using robotic or laparoscopic methods. Researchers want to understand how these surgical approaches may affect recovery and hospital stay. Participants will undergo a right hemicolectomy with an anastomosis created either inside the body (intra-corporeal) or outside the body (extra-corporeal) through minimally invasive techniques. The study randomly assigns patients to one of these two surgical methods. Both approaches involve removing portions of the colon and related blood vessels as needed. During the study, researchers will monitor how quickly bowel function returns by tracking passage of gas and bowel movements up to two weeks after surgery. They will also assess hospital length of stay, incision size, use of narcotic pain medications, surgical site infections, complications around the time of surgery, and operating room costs. Follow-up evaluations will occur up to six weeks after surgery to assess outcomes and safety.

CONDITIONS

Brief Title

Intra-Corporeal Anastomosis Result in Quicker Return of Bowel Function/Earlier Discharge

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults 18 years of age or older
  • Scheduled for a right hemicolectomy using a minimally invasive approach (robotic or laparoscopic) with an anastomosis
  • Right colectomy defined as removal of the ascending colon and related blood vessels, with possible removal of terminal ileum, proximal transverse colon, or right branch of the middle colic artery
Not Eligible

You will not qualify if you...

  • Pregnant women
  • Planned additional colon surgeries such as left colectomy or proctectomy
  • Vulnerable populations including prisoners or adults unable to give consent
  • Scheduled surgery at Butterworth hospital
  • Emergency surgery cases
  • Intra-operative exclusions: conversion to open surgery or performance of a loop ileostomy in addition to right colectomy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Surgery day

Participants undergo minimally invasive right hemicolectomy surgery with an intra-corporeal or extra-corporeal anastomosis and receive immediate post-operative care.

1 visit (in-person surgery and immediate recovery)

Post-operative Follow-up

Duration - Up to 6 weeks

Participants are followed up to monitor return of bowel function, inpatient length of stay, incision healing, narcotic use, surgical site infection, and perioperative morbidity.

Approximately 6 post-operative visits

Trial Site Locations

Total: 1 location

1

Spectrum Health Medical Group

Grand Rapids, Michigan, United States, 49546

Actively Recruiting

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Research Team

K

kendra Selby

E

Ellen Derrer

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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