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Evaluate the Possible Efficacy and Safety of Empagliflozin in Patient With Ulcerative Colitis

Primary Purpose

Ulcerative Colitis

Status
Not yet recruiting
Phase
Early Phase 1
Locations
Study Type
Interventional
Intervention
Empagliflozin
conventional treatment
Sponsored by
Tanta University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: •Patients with mild to moderate UC are diagnosed by history, clinical signs according to the Montreal classification of severity of ulcerative colitis and( Endoscopy, and biopsy) to establish the chronicity of inflammation and to exclude other causes of colitis. Exclusion Criteria: Other inflammatory bowel diseases (CD). History of serious hypersensitivity to empagliflozin or any component of the formulation. Patients on dialysis. Severe renal impairment (eGFR <20 ml/minute/1.73m2) . Chronic urinary tract infection. Chronic genital infection.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Experimental

    Arm Label

    placebo group

    empagliflozin group

    Arm Description

    Patients will receive conventional treatment only (corticosteroids +immune suppressive +amino salicylic acid) for 4 months.

    Patients will receive conventional treatment (corticosteroids +immune suppressive + aminosalicylic acid) and empagliflozin (0.4 - 0.5mg/kg/day) orally (maximum dose 25mg per day)for 4months.

    Outcomes

    Primary Outcome Measures

    clinical improvement of patients of mild to moderate UC using using the Montreal classification of severity of ulcerative colitis.
    difference between the two groups in (number of stool per day+prescence of fever +present of systemic toxicity+hemoglibin +ESR)

    Secondary Outcome Measures

    expression of TNFalpha
    difference between the two groups in TNFalpha
    expression of Adenosine monophosphate kinase (9AMPK ).
    difference between the two groups in Adenosine monophosphate kinase (9AMPK )
    expression of Fecal calprotectin
    difference between the two groups in fecal calprotectin

    Full Information

    First Posted
    October 31, 2022
    Last Updated
    November 9, 2022
    Sponsor
    Tanta University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05610956
    Brief Title
    Evaluate the Possible Efficacy and Safety of Empagliflozin in Patient With Ulcerative Colitis
    Official Title
    Clinical Study to Evaluate the Possible Efficacy and Safety of Empagliflozin in Patients With Ulcerative Colitis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 1, 2022 (Anticipated)
    Primary Completion Date
    December 1, 2023 (Anticipated)
    Study Completion Date
    December 1, 2026 (Anticipated)

    3. Sponsor/Collaborators

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

    4. Oversight

    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
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    •This study will be a randomized, controlled, parallel study. .To demonstrate the efficacy of empagliflozin and clinical improvement in patients of mild to moderate UC using the Montreal classification of severity of ulcerative colitis.
    Detailed Description
    It will be conducted on 60 patients having with mild to moderate degree UC divided into two groups: Group 1 (n=30): Patients will receive conventional treatment only (corticosteroids +immune suppressive +amino salicylic acid). Group 2 (n=30): Patients will receive conventional treatment (corticosteroids +immune suppressive + aminosalicylic acid) and empagliflozin (0.4 - 0.5mg/kg/day) orally (maximum dose 25mg per day). The patient will be selected from the Gastroenterology and Endoscopy Unit, Internal Medicine. . All patients will be subjected to the following: Complete history taking. Colonoscopy with intubation of the ileum and biopsies of affected and unaffected areas should be obtained to confirm the diagnosis of UC. Blood sample collection to assess: A) Routine Laboratory tests Complete blood picture (CBC). Liver functions (ALT, AST, Total and Direct Bilirubin). Kidney functions tests (Urea, serum creatinine). C-reactive protein. Fasting blood glucose. Urine analysis. B) Specific Laboratory tests 1. Tumor necrosis factor alpha (TNF-α). 2. Adenosine monophosphate kinase (9AMPK). 3. Fecal calprotectin. All patients will be assessed at baseline and after 4 months of therapy for all parameters

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Ulcerative Colitis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Early Phase 1
    Interventional Study Model
    Parallel Assignment
    Model Description
    parallel randomized controlled
    Masking
    ParticipantInvestigator
    Masking Description
    double blinded study
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    placebo group
    Arm Type
    Placebo Comparator
    Arm Description
    Patients will receive conventional treatment only (corticosteroids +immune suppressive +amino salicylic acid) for 4 months.
    Arm Title
    empagliflozin group
    Arm Type
    Experimental
    Arm Description
    Patients will receive conventional treatment (corticosteroids +immune suppressive + aminosalicylic acid) and empagliflozin (0.4 - 0.5mg/kg/day) orally (maximum dose 25mg per day)for 4months.
    Intervention Type
    Drug
    Intervention Name(s)
    Empagliflozin
    Intervention Description
    Patients will receive empagliflozin (0.4 - 0.5mg/kg/day) orally (maximum dose 25mg per day)and conventional treatment (corticosteroids +immune suppressive + aminosalicylic acid)for 4 months.
    Intervention Type
    Drug
    Intervention Name(s)
    conventional treatment
    Intervention Description
    conventional treatment (corticosteroids +immune suppressive + aminosalicylic acid)for 4 months
    Primary Outcome Measure Information:
    Title
    clinical improvement of patients of mild to moderate UC using using the Montreal classification of severity of ulcerative colitis.
    Description
    difference between the two groups in (number of stool per day+prescence of fever +present of systemic toxicity+hemoglibin +ESR)
    Time Frame
    4months
    Secondary Outcome Measure Information:
    Title
    expression of TNFalpha
    Description
    difference between the two groups in TNFalpha
    Time Frame
    4months
    Title
    expression of Adenosine monophosphate kinase (9AMPK ).
    Description
    difference between the two groups in Adenosine monophosphate kinase (9AMPK )
    Time Frame
    4months
    Title
    expression of Fecal calprotectin
    Description
    difference between the two groups in fecal calprotectin
    Time Frame
    4months

    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 mild to moderate UC are diagnosed by history, clinical signs according to the Montreal classification of severity of ulcerative colitis and( Endoscopy, and biopsy) to establish the chronicity of inflammation and to exclude other causes of colitis. Exclusion Criteria: Other inflammatory bowel diseases (CD). History of serious hypersensitivity to empagliflozin or any component of the formulation. Patients on dialysis. Severe renal impairment (eGFR <20 ml/minute/1.73m2) . Chronic urinary tract infection. Chronic genital infection.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    youmna hamdy eldeeb, phD
    Phone
    01014860930
    Email
    youmnahamdyeldeeb@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Sahar mohamed Elhaggar
    Phone
    01008838807

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
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