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Recruiting NCT07083076

NCT07083076 Regular Diet Versus Extended Low Residue After Colon Surgery

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Clinical Trial Summary
NCT ID NCT07083076
Status Recruiting
Phase
Sponsor Northwell Health
Condition Colon Resection
Study Type INTERVENTIONAL
Enrollment 222 participants
Start Date 2025-09-19
Primary Completion 2026-07-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Short term (10 day) low residue diet restriction6 week low residue diet restriction

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 222 participants in total. It began in 2025-09-19 with a primary completion date of 2026-07-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this clinical trial is to learn if a 10 day low-residue diet restriction is better for bowel function and quality of life without increasing complications compared to a 6 week low-residue diet restriction after elective colon resection surgery. The main questions it aims to answer are: Does a shorter time period of low residue restriction result in a faster return to normal bowel function? Are there any differences in complication rate between a 10 day low-residue diet restriction compared to a 6 week low-residue diet restriction? Participants will be randomized to one of the two diet plans and will be asked to answer surveys about their bowel function and health care related quality of life at various time points for up to 3 months.

Eligibility Criteria

Inclusion Criteria: * Adult patients who have elective colon resection with anastomosis Exclusion Criteria: * Patients who have an ostomy as part of their surgery * Patients who undergo emergency surgery * Patients who do not follow the enhanced recovery protocol (the standard postoperative protocol for patients undergoing elective colon resection) * Patients less than 18 years of age * Vulnerable populations: fetuses, pregnant women, children, cognitively impaired, hospital employees, students, healthy controls, prisoners, and other institutionalized individuals

Contact & Investigator

Central Contact

Andrea Zimmern, MD

✉ azimmern@northwell.edu

📞 516-730-2100

Principal Investigator

Andrea Zimmern, MD

PRINCIPAL INVESTIGATOR

Northwell Health

Frequently Asked Questions

Who can join the NCT07083076 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Colon Resection. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07083076 currently recruiting?

Yes, NCT07083076 is actively recruiting participants. Contact the research team at azimmern@northwell.edu for enrollment information.

Where is the NCT07083076 trial being conducted?

This trial is being conducted at Manhasset, United States, New Hyde Park, United States.

Who is sponsoring the NCT07083076 clinical trial?

NCT07083076 is sponsored by Northwell Health. The principal investigator is Andrea Zimmern, MD at Northwell Health. The trial plans to enroll 222 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology