- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04800861
Glycemic Control in Diabetic Hospitalized Patients
December 23, 2022 updated by: AlFayhaa General Hospital
Glycemic Control in Diabetic Hospitalized Patients: a Cross Sectional Study
With the advanced management of diabetes and new innovative anti-hyperglycemic therapy hyperglycemia remains a culprit factor affecting the outcome of patients admitted to the hospital in general wards.
Efforts from health care providers to assess and control blood sugar by a simplified method such as certified point of care hand-sized glucometers is the fruitful protocol if the results near the target that is endorsed by well-known diabetes societies.
In non-critically patients the premeal blood sugar ≤140 mg /dl and ≤ 180 mg /dl after a meal.
The unstable economy and political crises with the pandemic of Covid-19 making us use a glucometer to monitor and control the fluctuation of blood sugar in order to decrease the burden on the patients and health care providers in the form of a stay in the hospital and minimize wasting laboratory resources.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
120
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Alhasan M Al-Mudhaffer, BCPS
- Phone Number: +9647801601693
- Email: user11126@gmail.com
Study Locations
-
-
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Basra, Iraq, 99999
- AlFayhaa Teaching hospital
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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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
diabetic patients admitted in the hospital
Description
Inclusion Criteria:
- admitted to the hospital
Exclusion Criteria:
- none
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
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
glycemic control
Time Frame: From hospital admission to hospital discharge for a median of 7 days and up to 1 month
|
percentage of patients with glucose measurement (Random Blood Sugar, RBS, Fasting Blood Sugar, FBS) between 140-180 measured with bedside glucometers preferably before meals and at 6 am for fasting blood sugars or as directed by the physician
|
From hospital admission to hospital discharge for a median of 7 days and up to 1 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
average blood glucose value per ward
Time Frame: From hospital admission to hospital discharge for a median of 7 days and up to 1 month
|
average blood glucose value per ward (medical vs. surgical vs ICU/CCU
|
From hospital admission to hospital discharge for a median of 7 days and up to 1 month
|
average per patient
Time Frame: From hospital admission to hospital discharge for a median of 7 days and up to 1 month
|
average blood glucose levels per patient
|
From hospital admission to hospital discharge for a median of 7 days and up to 1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: AbdulSattar J Yousif, MD, Al-Fayhaa teaching hospital
- Study Chair: Ali Hussein A Alhamza, MD, Al-Fayhaa teaching hospital
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)
January 1, 2021
Primary Completion (Actual)
July 1, 2021
Study Completion (Actual)
July 1, 2021
Study Registration Dates
First Submitted
March 5, 2021
First Submitted That Met QC Criteria
March 14, 2021
First Posted (Actual)
March 16, 2021
Study Record Updates
Last Update Posted (Actual)
December 27, 2022
Last Update Submitted That Met QC Criteria
December 23, 2022
Last Verified
March 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1121
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
unidentified patient data will be shared if requested
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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