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Effect of Ptyrone on diabetes

An open labelled Study of Ptyrone in patients with treated uncontrolled type 2 diabetes mellitus

Status
Active, not recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019446
Enrollment
100
Registered
2019-05-30
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: E119- Type 2 diabetes mellitus without complications

Interventions

Intervention1: Ptyrone: 2 Capsules (425 mg/Capsule)orally for two times in a day for 12 weeks Control Intervention1: NA: NA

Sponsors

SSV Phytopharmaceuticals
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Male and female aged 18 to 65 who are suffering from type 2 diabetes mellitus. 2.Willing to give informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients who are suffering from any other systemic illness other than type 2 diabetes mellitus or megaloblastic anaemia. 2.Patients who are on corticosteroids and oral contraceptives 3.Patients with seropositive status. 4.Pregnancy 5.Patients Participation in clinical trials evaluating investigational pharmaceuticals or biologics within 3 months or devices within 30 days of admission to the study. 6.History of alcohol. substance abuse or alcoholism, within the previous one year

Design outcomes

Primary

MeasureTime frame
The primary objective of the study is to evaluate the activity and tolerability of Ptyrone in patients with treated uncontrolled type 2 diabetes mellitus.Timepoint: 12 weeks

Secondary

MeasureTime frame
Safety and tolerability; clinical and metabolic variables.Timepoint: 12 weeks

Countries

India

Contacts

Public ContactYogesh Dound

Kokan Hospital

milinddevale75@gmail.com

Outcome results

None listed

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