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Role of Linagliptin and Dapagliflozin versus Vildagliptin and Dapagliflozin in Diabetes patients

Efficacy and safety of Linagliptin and Dapagliflozin versus Vildagliptin and Dapagliflozin in Type 2 Diabetes mellitus: A Randomized controlled trial - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/04/066007
Enrollment
48
Registered
2024-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E119- Type 2 diabetes mellitus without complications

Interventions

Intervention1: Dapagliflozin plus Linagliptin: Fixed drug combination of Dapagliflozin(10 mg) plus Linagliptin (5mg) will be given once daily via oral route for 3 months. Control Intervention1: Dapagl

Sponsors

All India Institute of Medical Sciences, Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Age 18 to 65yr 2. Diagnosis of type 2 diabetes mellitus as per ADA criteria. 3. Newly diagnosed Type 2 DM patients. 4. Previously diagnosed DM patient on lifestyle modifications and anti-diabetic drugs. HbA1c more than 7 percentage.

Exclusion criteria

Exclusion criteria: 1. History of cardiac diseases (NYHA grade 3 – 4) or cardiac anomalies 2. Renal insufficiency - serum creatinine more than or equal to 1.8mg/dl 3. Patients with significant thyroid dysfunction and hepatic impairment (serum bilirubin more than 4. times, AST, ALT, and ALP more than three times the upper limit of normal) 5.Patient have any malignancy 6.Patient have any substance abuse(alcohol/drugs) 7.Pregnant & Lactating Woman 8.Those being treated with any investigational drug within the last 30 days 9.The patient is with severe illness/ infections  HbA1c more than 11%

Design outcomes

Primary

MeasureTime frame
To compare the effect of combination of dapagliflozin plus linagliptin versus dapagliflozin plus vildagliptin on HbA1c in T2 DM after 3 months from baselineTimepoint: 3 months from baseline

Secondary

MeasureTime frame
To evaluate the effect on fasting blood glucose (FBG) and HOMA index (HOMA-IR and HOMA- beta cell function) of dapagliflozin plus linagliptin versus dapagliflozin plus vildagliptin in T2 DM after 3 months from baseline.Timepoint: 3 months from baseline;To evaluate the effect on lipid profile parameters of dapagliflozin plus linagliptin versus dapagliflozin plus vildagliptin in T2 DM after 3 months from baseline.Timepoint: 3 months from baseline.;To evaluate the effect on QOL score (DQOL) of dapagliflozin plus linagliptin versus dapagliflozin plus vildagliptin in T2 DM after 3 months from baselineTimepoint: 3 months from baseline;To evaluate the safety of dapagliflozin plus linagliptin versus dapagliflozin plus vildagliptin in T2 DM over 3 monthsTimepoint: 3 months from baseline

Countries

India

Contacts

Public ContactIsha Yadav

AIIMS Jodhpur

yadavisha.2411@gmail.com8209302725

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026