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Effect of local insulin therapy versus standard dressing on healing in diabetic foot ulcer

Comparison Between Local Insulin Injection Therapy and Simple Dressing on Wound Vascularisation in Patient With Diabetic Foot Ulcer: A Randomised Control Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/089382
Enrollment
52
Registered
2025-06-23
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: E116- Type 2 diabetes mellitus with other specified complications

Interventions

Intervention1: Injectmncxnc: hxiuhiuashuiq Intervention2: Local injection of long acting insulin over diabetic foot ulcer: In Intervention group half the dose of calculated isophane insulin will be di

Sponsors

Dr Sandeep Singh
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Confirmed diagnosis of diabetes mellitus with HbA1c between 7-9% 2) Presence of a diabetic foot ulcer with duration exceeding three weeks 3) Patients willing to participate and provide informed consent 4) Patients able to comply with the study protocol and follow-up requirements

Exclusion criteria

Exclusion criteria: 1) Patients with extensive or complete necrosis requiring immediate amputation 2) Patients undergoing immunosuppressive therapy, radiotherapy, or treatment with corticosteroids or anticoagulants 3) Patients with peripheral vascular disease 4) Patients with any malignancy 5) Patients unable to comply with the study protocol or follow-up requirements 6) Patients who decline to participate or are unable to provide informed consent 7) Pregnant women and nursing mothers

Design outcomes

Primary

MeasureTime frame
Angiogenesis as measured by CD34 expression through immunohistochemical stainingTimepoint: Angiogenesis as measured by CD34 expression through immunohistochemical staining on day 0, day 5 and day 12

Secondary

MeasureTime frame
Reduction in wound surface area (measured in cm ) Timepoint: on day 0 and day 12;Wound contraction percentageTimepoint: On day 0 and day 12

Countries

India

Contacts

Public ContactDr Manabendra Baidya

Government Institute of Medical Sciences

manabendra306@gmail.com8874798762

Outcome results

None listed

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