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Spots Global Cancer Trial Database for Continuous Glucose Monitoring for Colorectal Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Continuous Glucose Monitoring for Colorectal Cancer

Official Title: Continuous Glucose Monitoring for Colorectal Cancer

Study ID: NCT06011473

Study Description

Brief Summary: Hyperglycemia commonly occurs during surgery due to a reaction to metabolic stress and trauma. It has been shown that improper glycemia control leads to impaired wound healing and a higher risk of other postoperative complications. The primary aim of our project is to assess the feasibility of the use of continuous glucose monitoring in measuring blood glucose levels in patients undergoing colorectal cancer surgery. The secondary aim is to analyze changes in perioperative blood glucose levels to understand the effects of stress and intraoperative interventions on the blood glucose level. The tertiary goal is to assess the predictive value of hyperglycemia for surgical site infection.

Detailed Description: Hyperglycemia commonly occurs during surgery due to a reaction to metabolic stress and trauma. It has been shown that improper glycemia control leads to impaired wound healing and a higher risk of other postoperative complications. However, glucose levels measured in patients before surgery are taken infrequently, and there remains controversy regarding optimal management. Usually, a blood glucose meter is used to measure non-fasted blood glucose concentrations, and a single-point measurement can easily misrepresent the actual glycemic control. Continuous glucose monitoring allows for a minimally invasive real-time remote glycemia control and is providing insights into glucose regulation in patients, demonstrating significant periods of clinically silent hypoglycemia and hyperglycemia. The primary aim of our project is to assess the feasibility of the use of CGM in measuring blood glucose levels in patients undergoing colorectal cancer surgery. The secondary aim is to analyze changes in perioperative blood glucose levels to understand the effects of stress and intraoperative interventions on the blood glucose level. The tertiary goal is to assess the predictive value of hyperglycemia for surgical site infection.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UCC Division of Oncological, Transplant and General Surgery, Gdańsk, Pomeranian, Poland

Contact Details

Name: Magdalena Antoszewska, MD

Affiliation: MUG Division of Dermatology, Venereology and Allergology

Role: PRINCIPAL_INVESTIGATOR

Name: Piotr Spychalski, MD, PhD

Affiliation: MUG Division of General Surgery

Role: PRINCIPAL_INVESTIGATOR

Name: Jarosław Kobiela, Prof.

Affiliation: MUG Division of General Surgery

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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