NCT07302464

Brief Summary

The work aimed to compare the effects of Sodium-glucose co-transporter-2 (SGLT2) inhibitors on glomerular filtration rate (GFR) in patients with diabetic chronic kidney disease (CKD) and non-diabetic CKD.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

December 11, 2025

Completed
13 days until next milestone

First Posted

Study publicly available on registry

December 24, 2025

Completed
Last Updated

December 24, 2025

Status Verified

December 1, 2025

Enrollment Period

8 months

First QC Date

December 11, 2025

Last Update Submit

December 11, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in the estimated glomerular filtration rate

    Change in the estimated glomerular filtration rate (eGFR) was recorded.

    6 months post-procedure

Study Arms (2)

Study group

Chronic kidney disease (CKD) participants with type 2 diabetes mellitus (T2DM)

Other: Sodium Glucose Co-Transporter 2 Inhibitors

Control group

Chronic kidney disease (CKD) participants without diabetes mellitus

Other: Sodium Glucose Co-Transporter 2 Inhibitors

Interventions

All candidates start therapy with sodium glucose co-transporter 2 (SGLT2) inhibitors with a dose of 10mg daily Dapagliflozin for 6 months

Control groupStudy group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

This case-control study was done on 60 adult chronic kidney disease (CKD) individuals with stage 3 and 4 (eGFR\>\_20ml/min/1.73 m2) according to KIDGO classification at Ain Shams University Hospitals, Cairo, Egypt.

You may qualify if:

  • Age ≥ 18 years.
  • Both sexes.
  • Chronic kidney disease (CKD) participants with stages 3 and 4.

You may not qualify if:

  • Patients with type 1 diabetes mellitus (DM).
  • Patients with decompensated Chronic liver disease.
  • Patients with uncontrolled hypertension.
  • Patients with blood pressure (BP) \> 110/70.
  • Patients already on the same medication (Sodium Glucose Co-Transporter 2 Inhibitors).
  • Patients with a history of recurrent or recent urinary tract infection (UTI).
  • Patients with glycated hemoglobin (HbA1c) ≤10.
  • Adult polycystic kidney disease.
  • All patients on immunosuppressive medications.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ain Shams University

Cairo, 11591, Egypt

Location

MeSH Terms

Conditions

Diabetes MellitusRenal Insufficiency, Chronic

Condition Hierarchy (Ancestors)

Glucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System DiseasesRenal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Internal Medicine and Nephrology, Faculty of Medicine, Ain shams University, Cairo, Egypt

Study Record Dates

First Submitted

December 11, 2025

First Posted

December 24, 2025

Study Start

October 1, 2024

Primary Completion

June 1, 2025

Study Completion

June 1, 2025

Last Updated

December 24, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will share

The data will be available upon a reasonable request from the corresponding author after the end of study for one year.

Shared Documents
STUDY PROTOCOL
Time Frame
After the end of study for one year.
Access Criteria
The data will be available upon a reasonable request from the corresponding author.

Locations