Weill Cornell Medicine-Section of Colon and Rectal Surgery
New York, 10021, United States
Location status: Recruiting
Location contact
KM Muktasid
CONTACT
Mehraneh Jafari, MD
PRINCIPAL_INVESTIGATOR
Yasmeen Chahal, MD
CONTACT
NCT Number: NCT07540845
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.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
New York, 10021, United States
Location status: Recruiting
KM Muktasid
CONTACT
Mehraneh Jafari, MD
PRINCIPAL_INVESTIGATOR
Yasmeen Chahal, MD
CONTACT
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will be advised to assume their regular diet post-operatively.
Patients who were educated on and prescribed a low-fiber diet postoperatively.
Time frame: 30 Days post-operative
Time frame: 30 Days Post-Operatively
Time frame: 30 Days Post-Operatively
If more than >70% subject complete the study, it will have been considered feasible.
Time frame: 30 Days Post-Operatively
Withdrawal by Post-Op Day 30
Time frame: 30 Days Post-Operatively
Contact information is provided by the study sponsor or research team.
KM Clinical Research Specialist
CONTACT
Yasmeen Research Fellow
CONTACT
Weill Medical College of Cornell University
Other
Impact of Postoperative Regular Diet on Colorectal Outcomes and Patient Quality of Life
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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