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Dapagliflozin in Type 2 Diabetes Mellitus Patients (T2DM) With Nonalcoholic Fatty Liver Disease (NAFLD)

Primary Purpose

Nonalcoholic Fatty Liver Disease, Type 2 Diabetes

Status
Recruiting
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Dapagliflozin 10mg Tab
Placebo
Sponsored by
Rehab Werida
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nonalcoholic Fatty Liver Disease

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Type 2 diabetes mellitus patients.
  2. HbA1C < 8.5.
  3. Patients were They were having fatty liver changes on abdominal ultrasound and mild to moderate elevation of serum liver enzymes.
  4. BMI more than 30

Exclusion Criteria:

  1. Patients with a history of alcohol, smoking, uncontrolled diabetes.
  2. (HbA1c > 9.0).
  3. Pregnancy.
  4. Lactation.
  5. Hemochromatosis.
  6. Thyroid disorders.
  7. Renal dysfunction.
  8. Cardiac problem.
  9. Chronic liver and decompensated liver disease in the form of hepatitis B and C.

Sites / Locations

  • Rehab Hussein WeridaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

group (A) for controlled (placebo).

group (D) for Dapagliflozin.

Arm Description

25 patients will recieve placebo for 6 months.

25 patients will recieve 10 mg Dapagliflozin daily for 6 months.

Outcomes

Primary Outcome Measures

leptin (ng/ml)
leptin by enzyme-linked immunosorbent assay (ELISA).
adiponectin (pg/ml)
adiponectin by enzyme-linked immunosorbent assay (ELISA).
VCAM-1 (ng/ml)
VCAM-1 was analyzed in serum using the human VCAM-1 ELISA kits.

Secondary Outcome Measures

Full Information

First Posted
July 12, 2022
Last Updated
September 26, 2023
Sponsor
Rehab Werida
Collaborators
University of Alexandria
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1. Study Identification

Unique Protocol Identification Number
NCT05459701
Brief Title
Dapagliflozin in Type 2 Diabetes Mellitus Patients (T2DM) With Nonalcoholic Fatty Liver Disease (NAFLD)
Official Title
The Hepato-protective Effect of Dapagliflozin in Type 2 Diabetes Mellitus Patients (T2DM) With Nonalcoholic Fatty Liver Disease (NAFLD)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 1, 2022 (Actual)
Primary Completion Date
December 30, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rehab Werida
Collaborators
University of Alexandria

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to evaluate the effect of dapagliflozin on liver function of patient with NAFLD and T2DM.
Detailed Description
Ethical committee approval will be obtained from Ethics committee of Faculty of Pharmacy, Damanhour University. Ethical committee approval will be obtained from Ethics committee of General Organization for Teaching Hospitals and Institutes. About 50 patients who are candidate to detect the hepato-protective effect of Dapagliflozin on non- alcoholic fatty disease, will be recruited from Alexandria Teaching Hospital (EL-Mery), General Organization for Teaching Hospitals and Institutes. All participants should agree to take part in this clinical study and will provide informed consent. Demographic data; age (year), sex (female/male), weight (kg), height (cm), BMI (kg/m2) will be collected. Venous blood samples (5 ml will be collected by a sterile syringe then placed in a suitable sterile tube to be centrifuged, the serum will be reserved and stored at -80°C until the analysis) before, and after receiving medication (Dapagliflozin). Measuring outcome: The biochemical tests will be done on the patients are alanine aminotransferase (ALT), aspartate aminotransferase (AST), homeostasis model assessment of insulin resistance (HOMA-IR), Hemoglobin A1C (HbA1C), Low-density lipoproteins (LDL), High-density lipoproteins (HDL), Triglycerides (TG), liver fibrosis score, and complete blood count (CBC). The molecular tests will be done on the patient are soluble vascular cell adhesion molecule-1 (Svcam-1), adipocytes (e.g. adiponectin, leptin). The ultrasound screening will be done at first examination. Statistical tests appropriate to the study design will be conducted to evaluate the significance of the results. Results, conclusion, discussion and recommendations will be given.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nonalcoholic Fatty Liver Disease, Type 2 Diabetes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
This is a prospective, randomized (1:1), double-blind clinical trial, will be carried out on 50 patients who are candidate to detect the hepato-protective effect of Dapagliflozin on diabetic type 2 patients with non- alcoholic fatty disease (dapagliflozin 10 mg once daily for 24 - 48 weeks -Patients will be randomly allocated into two equal groups (25 patients each); group (A) for controlled (placebo), and the other group (D) for Dapagliflozin.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
group (A) for controlled (placebo).
Arm Type
Placebo Comparator
Arm Description
25 patients will recieve placebo for 6 months.
Arm Title
group (D) for Dapagliflozin.
Arm Type
Active Comparator
Arm Description
25 patients will recieve 10 mg Dapagliflozin daily for 6 months.
Intervention Type
Drug
Intervention Name(s)
Dapagliflozin 10mg Tab
Other Intervention Name(s)
Dapagliflozin 10 mg.
Intervention Description
Dapagliflozin 10 mg once daily for 24 weeks.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
leptin (ng/ml)
Description
leptin by enzyme-linked immunosorbent assay (ELISA).
Time Frame
6 months
Title
adiponectin (pg/ml)
Description
adiponectin by enzyme-linked immunosorbent assay (ELISA).
Time Frame
6 months
Title
VCAM-1 (ng/ml)
Description
VCAM-1 was analyzed in serum using the human VCAM-1 ELISA kits.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Type 2 diabetes mellitus patients. HbA1C < 8.5. Patients were They were having fatty liver changes on abdominal ultrasound and mild to moderate elevation of serum liver enzymes. BMI more than 30 Exclusion Criteria: Patients with a history of alcohol, smoking, uncontrolled diabetes. (HbA1c > 9.0). Pregnancy. Lactation. Hemochromatosis. Thyroid disorders. Renal dysfunction. Cardiac problem. Chronic liver and decompensated liver disease in the form of hepatitis B and C.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rehab H Werida, Ass Prof.
Phone
+201005359968
Email
rehabwrieda@pharm.dmu.edu.eg
First Name & Middle Initial & Last Name or Official Title & Degree
Yasmine Essam, Bachlor
Email
Y.essam02001@pharm.dmu.edu.eg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rehab H Werida, Ass Prof.
Organizational Affiliation
Damanhour University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Amira B. Kassem, Lecturer
Organizational Affiliation
Damanhour University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yasmin Essam, Bachlor
Organizational Affiliation
Damanhour University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehab Hussein Werida
City
Damanhūr
State/Province
Elbehairah
ZIP/Postal Code
31527
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rehab H Werida
Phone
01005359968
Email
rehabwrieda@pharm.dmu.edu.eg
First Name & Middle Initial & Last Name & Degree
Jassmin Essam
Phone
01555973972
Email
Y.essam02001@pharm.dmu.edu.eg

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26963613
Citation
Chiba Y, Yamada T, Tsukita S, Takahashi K, Munakata Y, Shirai Y, Kodama S, Asai Y, Sugisawa T, Uno K, Sawada S, Imai J, Nakamura K, Katagiri H. Dapagliflozin, a Sodium-Glucose Co-Transporter 2 Inhibitor, Acutely Reduces Energy Expenditure in BAT via Neural Signals in Mice. PLoS One. 2016 Mar 10;11(3):e0150756. doi: 10.1371/journal.pone.0150756. eCollection 2016.
Results Reference
background
PubMed Identifier
23707905
Citation
Tahara A, Kurosaki E, Yokono M, Yamajuku D, Kihara R, Hayashizaki Y, Takasu T, Imamura M, Li Q, Tomiyama H, Kobayashi Y, Noda A, Sasamata M, Shibasaki M. Effects of SGLT2 selective inhibitor ipragliflozin on hyperglycemia, hyperlipidemia, hepatic steatosis, oxidative stress, inflammation, and obesity in type 2 diabetic mice. Eur J Pharmacol. 2013 Sep 5;715(1-3):246-55. doi: 10.1016/j.ejphar.2013.05.014. Epub 2013 May 23.
Results Reference
result
PubMed Identifier
26914659
Citation
Ohki T, Isogawa A, Toda N, Tagawa K. Effectiveness of Ipragliflozin, a Sodium-Glucose Co-transporter 2 Inhibitor, as a Second-line Treatment for Non-Alcoholic Fatty Liver Disease Patients with Type 2 Diabetes Mellitus Who Do Not Respond to Incretin-Based Therapies Including Glucagon-like Peptide-1 Analogs and Dipeptidyl Peptidase-4 Inhibitors. Clin Drug Investig. 2016 Apr;36(4):313-9. doi: 10.1007/s40261-016-0383-1.
Results Reference
result

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Dapagliflozin in Type 2 Diabetes Mellitus Patients (T2DM) With Nonalcoholic Fatty Liver Disease (NAFLD)

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