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Recruiting

NCT Number: NCT07540845

Regular Diet After Colorectal Surgery

The goal of this pilot study is to assess the safety and feasibility of regular diet after surgical removal of the colon. The study will enroll patients preoperatively, prior to colon surgery, and will follow participants for up to 30 days. The study hypothesizes that simplifying nutritional recommendations is safe and may improve quality of life.

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

Weill Cornell Medicine-Section of Colon and Rectal Surgery

New York, 10021, United States

Location status: Recruiting

Location contact

KM Muktasid

CONTACT

[email protected]

6469622270

Mehraneh Jafari, MD

PRINCIPAL_INVESTIGATOR

Yasmeen Chahal, MD

CONTACT

6469622270

About this study

This pilot study aims to establish the safety of a return to a regular diet after surgery. Patients scheduled to undergo removal of a piece of their colon will be recruited before surgery and placed on a regular diet after surgery. Participants in this trial will be compared with previous patients who have undergone a similar surgery but were educated on and prescribed a low-fiber diet after surgery. Measures relating to morbidity and 30-day readmission rate will be collected prospectively. Surgical complications will also be collected. Participants will complete surveys about anxiety and quality of life at various time points in the study.

The study will track the healthcare resources needed by participants during this study through a number of metrics, such as visits, phone calls, and messaging.

The overarching goals of this study are to determine if resuming a regular diet after surgery is safe, if it impacts quality of life, and whether it increases how often patients need to engage with the healthcare system. The study will also explore associations with patient anxiety and strain on the care team in the form of communications related to diet.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Male or female ≥ 18 years of age
  • Scheduled to undergo colorectal resection

Exclusion criteria

  • Patients with bowel obstructions
  • Patients below the age of 18

Treatment and study plan

Regular Diet Post-Operatively

Other

Participants will be advised to assume their regular diet post-operatively.

Historical Cohort: Low-Fiber Diet

Other

Patients who were educated on and prescribed a low-fiber diet postoperatively.

Primary outcomes

  1. Number of 30-day readmissions

    Time frame: 30 Days post-operative

  2. Surgery related morbidity

    Time frame: 30 Days Post-Operatively

Secondary outcomes

  1. Percent of participants who complete the study (Feasibility)

    Time frame: 30 Days Post-Operatively

    If more than >70% subject complete the study, it will have been considered feasible.

  2. Number of participants who drop out of the study

    Time frame: 30 Days Post-Operatively

    Withdrawal by Post-Op Day 30

  3. Number of participants removed from the study due to clinical determination

    Time frame: 30 Days Post-Operatively

Study contacts

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

KM Clinical Research Specialist

CONTACT

[email protected]

646-962-2789

Yasmeen Research Fellow

CONTACT

[email protected]

646-962-2789

Sponsors and collaborators

Lead sponsor

Weill Medical College of Cornell University

Other

Registry information

Official study title

Impact of Postoperative Regular Diet on Colorectal Outcomes and Patient Quality of Life

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 20, 2026
Registry last updated
May 22, 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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