- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03109951
Abnormal Blood Sugar Tests in Diabetic Patients During Colonoscopy Preparation
March 6, 2020 updated by: Myong Ki Baeg, Catholic Kwandong University
Type 2 diabetes is rapidly increasing globally and has been associated with an increased risk of colorectal cancer.
Therefore, the numbers of diabetic patients who will undergo colonoscopic screening are expected to grow exponentially.
Colonoscopic preparation entails prolonged fasting, cessation of anti-diabetic medication and ingestion of preparation medications.
This may put the diabetic patient at risk of potentially dangerous hypo- or hyperglycemia.
However, studies regarding the safety of colonoscopic preparation in diabetic are lacking.
In this study, the investigators aim to discover the prevalence of abnormal glucose levels in diabetic patients who undergo colonoscopy.
The investigators also aim to find out risk factors for abnormal glucose levels and develop a safe preparation protocol.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
- Type 2 diabetes subjects who will undergo colonoscopy will be prospectively enrolled when visiting the outpatient clinic.
- Subjects will be instructed to fast from 6pm of the day before colonoscopy.
- Subjects will be instructed to abstain from diabetes medication while the subjects fast.
- Subjects who are scheduled to undergo colonoscopy in the morning will take colonoscopy preparation medication (2L (liter) of polyethylene glycol with ascorbic acid) in a split dose (i.e. 1L from 8-10 pm of the day before colonoscopy and 1L 4-6 hours before colonoscopy). Those who will undergo colonoscopy in the afternoon will take 2L of the preparation medication 6 hours before colonoscopy.
- Subjects will be instructed to take the preparation medication at rate of 250 mL every 10 to 15 minutes.
- Upon arrival at the endoscopy center of International St. Mary's hospital, subjects will be given a self-administered questionnaire which will ask about their age, gender, duration of diabetes, type of diabetes medication, time of last diabetes medication taken, knowledge of hypo/hyperglycemia symptoms, previous hypo/hyperglycemia experience, self-treatment of hypoglycemia (if done), total amount of colonoscopy preparation medication ingested, total fasting time and time of last preparation medication ingested.
- Subjects will have vital signs (blood pressure, heart rate) taken and their capillary glucose levels checked using the Accu-Chek Performa.
- Any subjects with capillary glucose levels <70mg/dL or >250mg/dL will be reported to the attending physician. Those with an initial glucose level <70mg/dL will be given a piece of candy and have their glucose rechecked in 10 mins. Subjects will be asked if the hypoglycemic symptoms (if any) have abated. Those with a glucose level >250mg/dL will undergo hydration with normal saline at 120 ml/Hr. Those who do not respond to treatment or are in critical condition will be moved to the Emergency department for treatment. Subjects who respond to treatment will have their glucose levels checked after colonoscopy before undergoing discharge. Those with abnormal levels upon follow-up testing will be sent to either the endocrinology outpatient clinic or the emergency room depending on their clinical severity.
- All data will be recorded by initials with patient identities masked. All data will be kept in a locked and secure location by the principal investigator.
Study Type
Interventional
Enrollment (Actual)
187
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Incheon, Korea, Republic of, 22711
- International St.Mary's Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 75 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Type 2 diabetes
- Between ages of 20-75
- Undergo colonoscopy at International St. Mary's Hospital
Exclusion Criteria:
- Type 1 diabetes patients
- Did not undergo colonoscopy preparation
- Did not meet fasting requirements
- Have known current infectious diseases
- Have known cancer and/or are under cancer treatment
- Are under intravenous fluid therapy during colonoscopy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: OTHER
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
OTHER: Diabetes group
Type 2 diabetes patients undergoing colonoscopy with preparation with 2L of polyethylene glycol.
|
Colonoscopy preparation using standard preparation with 2L of polyethylene glycol.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Abnormal Glucose Levels After Colonoscopic Preparation
Time Frame: 30 minutes before colonoscopy
|
Count of patients with Serum glucose levels < 70mg/dL or >250mg/dL
|
30 minutes before colonoscopy
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cognition of Hypoglycemic Symptoms
Time Frame: 30 minutes before colonoscopy
|
Subjects awareness of hypoglycemic symptoms - by questionnaire 96 subjects were aware of hypoglycemic symptoms and could recognize them.
|
30 minutes before colonoscopy
|
|
Number of Participants With Self-treatment and Relief of Hypoglycemic Symptoms
Time Frame: From colonoscopy preparation beginning to day 1 after colonoscopy
|
Discover if self-treatment of hypoglycemic symptoms relieves hypoglycemia and associated symptoms
|
From colonoscopy preparation beginning to day 1 after colonoscopy
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Myong Ki Baeg, MD, PhD, International St. Mary's Hospital, Catholic Kwandong University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Vann MA. Perioperative management of ambulatory surgical patients with diabetes mellitus. Curr Opin Anaesthesiol. 2009 Dec;22(6):718-24. doi: 10.1097/ACO.0b013e3283310f51.
- Kollarits CR, Kendrick RM, Guess M. Perioperative treatment of patients with diabetes having eye surgery with local anesthesia in an ambulatory facility. Ophthalmic Surg Lasers Imaging. 2004 May-Jun;35(3):185-8.
- Joshi GP, Chung F, Vann MA, Ahmad S, Gan TJ, Goulson DT, Merrill DG, Twersky R; Society for Ambulatory Anesthesia. Society for Ambulatory Anesthesia consensus statement on perioperative blood glucose management in diabetic patients undergoing ambulatory surgery. Anesth Analg. 2010 Dec;111(6):1378-87. doi: 10.1213/ANE.0b013e3181f9c288. Epub 2010 Oct 1.
- Yao J, Zhang W, Chen J, Zhang G, Zheng S. Enteral nutrition before bowel preparation improves the safety of colonoscopy in the elderly. Turk J Gastroenterol. 2013;24(5):400-5. doi: 10.4318/tjg.2013.0638.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
March 25, 2017
Primary Completion (ACTUAL)
December 31, 2019
Study Completion (ACTUAL)
December 31, 2019
Study Registration Dates
First Submitted
April 3, 2017
First Submitted That Met QC Criteria
April 6, 2017
First Posted (ACTUAL)
April 12, 2017
Study Record Updates
Last Update Posted (ACTUAL)
March 20, 2020
Last Update Submitted That Met QC Criteria
March 6, 2020
Last Verified
March 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IS16OASI0026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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