Regular Diet After Colorectal Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorWeill Medical College of Cornell University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female ≥ 18 years of age

Scheduled to undergo colorectal resection

Disqualifiers

Patients with bowel obstructions

Patients below the age of 18

Trial design

Design model

Single group

Treatments tested in this trial

  • Regular Diet Post-Operatively

    Other intervention

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

  • Historical Cohort: Low-Fiber Diet

    Other intervention

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

Treatment groups

10 Participants
are divided into 2 treatment groups
Group A: Regular DietExperimental treatment 1 intervention
Group B: Historical ControlOther 1 intervention

Trial outcomes

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)

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

Time frame
30 Days Post-Operatively
2

Number of participants who drop out of the study

Withdrawal by Post-Op Day 30

Time frame
30 Days Post-Operatively
3

Number of participants removed from the study due to clinical determination

Time frame
30 Days Post-Operatively

Other outcomes

Sponsors and contacts

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