Intervention Effect of Canagliflozin on Prediabetes in Patients With HIV.
Primary Purpose
PreDiabetes, Hiv
Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Canagliflozin
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for PreDiabetes
Eligibility Criteria
Inclusion Criteria:
- Patients with HIV infection combined with prediabetes who are not treated with antidiabetic drugs
- Fasting blood glucose of 6.1-6.9 mmol/L or 2-hour oral glucose tolerance test of 7.8-11.0 mmol/L
- BMI >24 kg/m2 and no more than 10% weight fluctuation in 3 months
- HIV-infected patients must be on antiretroviral therapy, no significant symptoms, have HIV RNA below the lower limit of detection for 3 consecutive months, and have CD4 cells greater than 200/uL
Exclusion Criteria:
- Patients with diagnosed diabetes
- Those who are unwilling to participate or unable to cooperate
- The patient has had an acute heart attack or cardiovascular disease in the last three months
- Positive pancreatic islet autoimmune antibody
- History of pancreatitis or pancreatic cancer
- Pregnant or breastfeeding women
- Liver function aminotransferases greater than 2 times the upper limit of the normal range
- Patients with previous recurrent urinary tract infections
- Glomerular filtration rate <45ml/min/1.73m2
- Other serious co-morbidities
Sites / Locations
- Intervention Effect of Canagliflozin on Prediabetes in Patients With HIV: A Randomized Controlled Trial.Recruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Lifestyle interventions + Canagliflozin
Lifestyle interventions + Placebo
Arm Description
Subjects were instructed on diet and exercise and advised to make lifestyle changes while they were given daily oral doses of canagliflozin 100mg.
Subjects were instructed on diet and exercise and advised to make lifestyle changes while they were given daily oral doses of placebo 100mg.
Outcomes
Primary Outcome Measures
The rate of progression from prediabetes to diabetes one year after the intervention in both groups of subjects.
The rate of progression from prediabetes to diabetes one year after the intervention in both groups of subjects.
Secondary Outcome Measures
Changes in the amount of insulin and C-peptide produced in the two groups of subjects one year after the intervention.
To investigate the effect of canagliflozin on islet cells, the changes in the amount of insulin and C-peptide produced in two groups of subjects after one year of intervention were examined.
Changes in the number of CD4 T cells after one year intervention in the two groups.
To investigate whether canagliflozin affects immunity in HIV patients, detect number of CD4T cell changes one year after the intervention in both groups of subjects.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT05135039
Brief Title
Intervention Effect of Canagliflozin on Prediabetes in Patients With HIV.
Official Title
Intervention Effect of Canagliflozin on Prediabetes in Patients With HIV: A Randomized Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2022 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
xiaolong zhao
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The high prevalence of prediabetes in HIV patients is also an outpost event for the further development of diabetes and cardiovascular events, as well as for the prolonged survival of HIV patients with metabolic problems and their complications. Based on the well-established experience in the field of traditional diabetes with prediabetes, the combination of SGLT2 inhibitors can target the pathophysiological mechanisms of HIV-induced metabolic disorders, and the results of a small pilot study of one of the representative drugs, cabergoline, in HIV-combined diabetic patients suggest its efficacy and safety in the treatment of HIV-combined diabetic patients. Combined with the advantages of the concentrated disease resources of HIV patients in the investigator's unit, this study is intended to use a single-center randomized controlled clinical trial design, giving the experimental group drug combined with lifestyle intervention and the control group lifestyle combined with placebo intervention, to verify whether the combination of cabergoline and lifestyle intervention can safely and significantly change the clinical outcome of glucose metabolism, as well as the effect on body weight and pancreatic islet function of patients The study provides top clinical evidence for the treatment of these patients and suggests a new set of interventions for patients with HIV combined with prediabetes. No similar studies have been found to be innovative in the literature search, and the implementation of this study will be of great clinical value.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PreDiabetes, Hiv
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
218 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Lifestyle interventions + Canagliflozin
Arm Type
Experimental
Arm Description
Subjects were instructed on diet and exercise and advised to make lifestyle changes while they were given daily oral doses of canagliflozin 100mg.
Arm Title
Lifestyle interventions + Placebo
Arm Type
Placebo Comparator
Arm Description
Subjects were instructed on diet and exercise and advised to make lifestyle changes while they were given daily oral doses of placebo 100mg.
Intervention Type
Drug
Intervention Name(s)
Canagliflozin
Intervention Description
Canagliflozin 100mg/day/patient
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo 100mg/day/patient
Primary Outcome Measure Information:
Title
The rate of progression from prediabetes to diabetes one year after the intervention in both groups of subjects.
Description
The rate of progression from prediabetes to diabetes one year after the intervention in both groups of subjects.
Time Frame
one year
Secondary Outcome Measure Information:
Title
Changes in the amount of insulin and C-peptide produced in the two groups of subjects one year after the intervention.
Description
To investigate the effect of canagliflozin on islet cells, the changes in the amount of insulin and C-peptide produced in two groups of subjects after one year of intervention were examined.
Time Frame
one year
Title
Changes in the number of CD4 T cells after one year intervention in the two groups.
Description
To investigate whether canagliflozin affects immunity in HIV patients, detect number of CD4T cell changes one year after the intervention in both groups of subjects.
Time Frame
one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with HIV infection combined with prediabetes who are not treated with antidiabetic drugs
Fasting blood glucose of 6.1-6.9 mmol/L or 2-hour oral glucose tolerance test of 7.8-11.0 mmol/L
BMI >24 kg/m2 and no more than 10% weight fluctuation in 3 months
HIV-infected patients must be on antiretroviral therapy, no significant symptoms, have HIV RNA below the lower limit of detection for 3 consecutive months, and have CD4 cells greater than 200/uL
Exclusion Criteria:
Patients with diagnosed diabetes
Those who are unwilling to participate or unable to cooperate
The patient has had an acute heart attack or cardiovascular disease in the last three months
Positive pancreatic islet autoimmune antibody
History of pancreatitis or pancreatic cancer
Pregnant or breastfeeding women
Liver function aminotransferases greater than 2 times the upper limit of the normal range
Patients with previous recurrent urinary tract infections
Glomerular filtration rate <45ml/min/1.73m2
Other serious co-morbidities
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaolong Zhao, PhD
Phone
+862137990333
Ext
6261
Email
xiaolongzhao@163.com
First Name & Middle Initial & Last Name or Official Title & Degree
Xinyue Xu, master
Phone
+862137990333
Ext
6261
Email
xuxy530@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaolong Zhao, PhD
Organizational Affiliation
Shanghai Public Health Clinical Center
Official's Role
Study Chair
Facility Information:
Facility Name
Intervention Effect of Canagliflozin on Prediabetes in Patients With HIV: A Randomized Controlled Trial.
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200000
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaolong Zhao, PhD
Phone
+86 21 3799 0333
Ext
6261
Email
xiaolongzhao@163.com
First Name & Middle Initial & Last Name & Degree
Xinyue Xu, master
Phone
+86 21 3799 0333
Ext
6261
Email
xuxy530@163.com
First Name & Middle Initial & Last Name & Degree
Xinyue Xu, master
First Name & Middle Initial & Last Name & Degree
Xiaolong Zhao, PhD
12. IPD Sharing Statement
Learn more about this trial
Intervention Effect of Canagliflozin on Prediabetes in Patients With HIV.
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