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Nitazoxanide as Adjuvant Therapy in Type 2 Diabetes Mellitus

Primary Purpose

Diabetes Mellitus, Type 2

Status
Recruiting
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
Nitazoxanide
Sponsored by
Tanta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Glycated hemoglobin (HbA1c) between 7% and 9%. Body mass index ≥ 25 kg/m2 Exclusion Criteria: Pregnant or nursing women. Type 1 diabetes mellitus. Liver disease (alanine aminotransferase > 3 upper normal limit). Kidney disease (estimated glomerular filtration rate < 60 ml/min/1.73 m2). Inflammatory bowel diseases. History of allergy and/or adverse reactions to the drugs used in the study.

Sites / Locations

  • Faculty of medicine, Tanta UniversityRecruiting
  • Faculty of Medicine, Menoufia UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Group 1

Group 2

Arm Description

35 Patients with type 2 diabetes receiving treatment with metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors (such as vildagliptin).

35 Patients with type 2 diabetes receiving nitazoxanide 500 mg orally twice daily in addition to metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors (such as vildagliptin).

Outcomes

Primary Outcome Measures

Glycemic control
Fasting blood glucose and glycated hemoglobin

Secondary Outcome Measures

Insulin resistance
fasting insulin level with HOMA-IR calculation
Lipid profile
Serum levels of total cholesterol, LDL, HDL, and triglycerides
Serum levels of A-kinase anchoring protein 1
Serum levels of asprosin

Full Information

First Posted
August 21, 2023
Last Updated
August 21, 2023
Sponsor
Tanta University
Collaborators
Menoufia University
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1. Study Identification

Unique Protocol Identification Number
NCT06010992
Brief Title
Nitazoxanide as Adjuvant Therapy in Type 2 Diabetes Mellitus
Official Title
A Clinical Study Evaluating the Potential Benefit of Nitazoxanide in Patients With Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 1, 2023 (Anticipated)
Primary Completion Date
October 1, 2024 (Anticipated)
Study Completion Date
January 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tanta University
Collaborators
Menoufia University

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
Diabetes mellitus (DM) is a complex metabolic disorder characterized by hyperglycemia and abnormalities in carbohydrate, fat, and protein metabolism. Despite the advancement in anti-diabetic drug therapy, most patients fail to achieve optimal glycemic control. This highlights the need for more effective strategies to control type 2 diabetes mellitus. Nitazoxanide (NTZ), a broad-spectrum anti-infective drug with activity against various protozoa, helminthes, bacteria, and viruses, was identified as peroxisome proliferative activated receptor gamma (PPARγ) agonist using one dimensional drug profile matching. Additionally, it improved insulin sensitivity in insulin-resistant type 2 diabetic rats. Therefore, this study is designed to evaluate the efficacy of nitazoxanide as adjunctive therapy in patients with type 2 diabetes mellitus.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
No Intervention
Arm Description
35 Patients with type 2 diabetes receiving treatment with metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors (such as vildagliptin).
Arm Title
Group 2
Arm Type
Experimental
Arm Description
35 Patients with type 2 diabetes receiving nitazoxanide 500 mg orally twice daily in addition to metformin and dipeptidyl peptidase-4 (DPP-4) inhibitors (such as vildagliptin).
Intervention Type
Drug
Intervention Name(s)
Nitazoxanide
Intervention Description
Nitazoxanide oral capsules 500 mg twice daily
Primary Outcome Measure Information:
Title
Glycemic control
Description
Fasting blood glucose and glycated hemoglobin
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Insulin resistance
Description
fasting insulin level with HOMA-IR calculation
Time Frame
12 weeks
Title
Lipid profile
Description
Serum levels of total cholesterol, LDL, HDL, and triglycerides
Time Frame
12 weeks
Title
Serum levels of A-kinase anchoring protein 1
Time Frame
12 weeks
Title
Serum levels of asprosin
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Glycated hemoglobin (HbA1c) between 7% and 9%. Body mass index ≥ 25 kg/m2 Exclusion Criteria: Pregnant or nursing women. Type 1 diabetes mellitus. Liver disease (alanine aminotransferase > 3 upper normal limit). Kidney disease (estimated glomerular filtration rate < 60 ml/min/1.73 m2). Inflammatory bowel diseases. History of allergy and/or adverse reactions to the drugs used in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eman Ghonaim, Assistant lecturer
Phone
+20-010-970-821-57
Email
eman.ghonim@pharm.tanta.edu.eg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eman Ghonaim
Organizational Affiliation
Assistant Lecturer, Faculty of Pharmacy, Tanta University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of medicine, Tanta University
City
Tanta
State/Province
El-Gharbia
ZIP/Postal Code
31527
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eman Ghonaim
Phone
+20-010-970-821-57
Email
eman.ghonim@pharm.tanta.edu.eg
Facility Name
Faculty of Medicine, Menoufia University
City
Shibīn Al Kawm
State/Province
Menoufia
ZIP/Postal Code
32511
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eman Ghonaim
Phone
+20-010-970-812-57
Email
eman.ghonim@pharm.tanta.edu.eg

12. IPD Sharing Statement

Plan to Share IPD
No

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Nitazoxanide as Adjuvant Therapy in Type 2 Diabetes Mellitus

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