Assesment safety and efficacy of Ayurvedic Formulation AYUSH AGT in external wounds.
- Conditions
- Health Condition 1: - Health Condition 2: - Health Condition 3: L99- Other disorders of skin and subcutaneous tissue in diseases classified elsewhere
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
.1 Patients of either sex with age between 18 and 60 years
2 Patients with Superficial externalwounds requiring dressing
3. Solitary wound not less than 1 inches (2.5 cm) in diameter
4 Patienwilling to participate in the study for 1 month
1Known allergy/hypersensitivity to any of the components of the dressing
2.Wound associated with fracture
3.Wound associated with skin disorder that is chronic or currently active like psoriasis, eczema
4.Neurological deficit at wound site
5.Hemoglobin level <7.0 g/dl, serumalbumin <3 g/dl
6.Patients with concurrent Hepatic Dysfunction (defined as AST and/or ALT > 2 times of the upper normal limit) or Renal Dysfunction (defined as S.Creatinine > 1.2 mg/dl)
7.Known cases of Diabetes Mellitus, AIDS & other sexually
transmitted diseases, Malignancy or known history of coagulopathy
8.Patients receiving immune-suppressive medication
9.Pregnancy or lactation
10.Varicose veins/Deep Vein Thrombosis
11.Wounds requiring full thickness graft
12.Patients where a reference wound cannot be treated in isolation fromother wounds.
13.H/o hypersensitivity to any of thetrial drugs or their ingredients.
14.Patient taking participationin any other clinical trial
15.Any other condition which the Investigatorthinksmay jeopardize the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method