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NCT Number: NCT03862781

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

Adult patients who are regularly scheduled to undergo a right hemicolectomy via a minimally invasive approach (robotic or laparoscopic) with the creation of an anastomosis.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Corewell Health Medical Group

Grand Rapids, Michigan, 49546, United States

Location status: Recruiting

Location contact

James Ogilvie, MS

PRINCIPAL_INVESTIGATOR

Julia E reish

CONTACT

[email protected]

616-486-2022

Rachel R Gross

CONTACT

[email protected]

About this study

The purpose of this trial is to investigate whether minimally invasive right colectomies done with an intra-corporeal anastomosis result in quicker return of bowel function and earlier discharge. The primary endpoint of this study will be return of bowel function as measured by passage of flatus and bowel motions. The secondary endpoints will be inpatient length of stay, incision length, postoperative narcotic use, surgical site infection (superficial, deep and organ-space), perioperative morbidity and operating room charges.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Eligible patients are those over 18 years of age who are regularly scheduled to undergo a right hemicolectomy via a minimally invasive approach (robotic or laparoscopic) with the creation of an anastomosis. Right colectomy will be defined as removal of the ascending colon, ligation of the ileocolic artery and vein, +/- removal of the terminal ileum, +/- removal of the proximal transverse colon, and +/- removal of the right branch of the middle colic artery and vein.

Exclusion criteria

  • Pregnant women
  • Additional colon resection is planned (i.e. left colectomy or proctectomy)
  • Vulnerable populations such as prisoners or adults unable to give consent
  • If the scheduled surgery is planned at Butterworth hospital (as to standardize the nursing care received postoperatively)
  • Emergent cases

Patients will be excluded from the study intra-operatively if:

  • The procedure is converted to an open resection
  • If a loop ileostomy is performed in addition to the right colectomy

Treatment and study plan

Right Hemicolectomy

Procedure

Minimally invasive approach (robotic or laparoscopic) with the creation of an anastomosis.

Primary outcomes

  1. Return of bowel function

    Time frame: up to 2 weeks

    Flatus and bowel motions

Secondary outcomes

  1. Inpatient length of stay

    Time frame: up to 2 weeks

    Days in the hospital after surgery

  2. Incision length

    Time frame: Surgery date

    cm's

  3. Postoperative narcotic use

    Time frame: up to 2 weeks

    Average pain scores over first 5 hospital days

  4. Surgical site infection

    Time frame: up to 6 weeks

    (superficial, deep and organ-space)

  5. Perioperative morbidity

    Time frame: Baseline (Prior to surgery)

    Disease state

  6. Operating room charges

    Time frame: Surgery date

    Fees for operating room

Study contacts

Contact information is provided by the study sponsor or research team.

Ellen Derrer

CONTACT

[email protected]

kendra Selby

CONTACT

[email protected]

616-486-0281

Sponsors and collaborators

Lead sponsor

Corewell Health West

Other

Registry information

Official study title

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

Acronym: RICART

Important dates

Study start
2019
Primary completion
2026
Study completion
2027
First posted
Mar 5, 2019
Registry last updated
Jul 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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