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Review study on use of Galvus and Galvus/Met medicines

A drug utilization review of Galvus (vildagliptin) and GalvusMet (vildagliptin plus metformin fixed-drug combination) in type 2 diabetes mellitus - DUR

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
CTRI
Registry ID
CTRI/2016/06/006991
Enrollment
800
Registered
2016-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- Diagnosed with Type II diabetes mellitus

Interventions

None listed

Sponsors

Novartis Healthcare Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adult (>= 18 years) T2DM patients of both genders, who have been prescribed vildagliptin or vildagliptin-metformin fixed-dose combination (Galvus or GalvusMet). 2.Written informed consent will be obtained from patients for use of their data in hospital database for the purpose of research

Exclusion criteria

Exclusion criteria: Not applicable

Design outcomes

Primary

MeasureTime frame
To assess the utilization of vildagliptin-metformin FDC in real-world scenario. Timepoint: Data would be collected from hospital medical records of patients with type 2 diabetes mellitus, who have been prescribed vildagliptin or its combination as per the discretion of the physician, during the study period (June 2016 - June 2017)

Secondary

MeasureTime frame
To assess the utilization pattern of vildagliptin and its combinations in real-world scenario.Timepoint: Data would be collected from hospital medical records of patients with type 2 diabetes mellitus, who have been prescribed vildagliptin or its combination as per the discretion of the physician, during the study period (June 2016 - June 2017)

Countries

India

Contacts

Public ContactDr Smit Shah

Novartis Healthcare Private Limited

smit.shah@novartis.com912224958863

Outcome results

None listed

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