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To Study The Efficacy Of An Ultrasonic Cavitation Machine With Mahavishgarbha gel on the disease of Lipoma in the age Group 18-60 Years.

Randomized Clinical Study On Lipoma By Using Ultrasonic Cavitation Machine With Mahavishgarbha Gel In The Age Group Of 18-60 Years. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/06/088213
Enrollment
80
Registered
2025-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-06-24

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

Conditions

Health Condition 1: L99- Other disorders of skin and subcutaneous tissue in diseases classified elsewhere

Interventions

Intervention1: Nil: Nil Intervention2: Nil: Nil Intervention3: Nil: Nil

Sponsors

DMM Ayurved Mahavidyalaya,Yavatmal
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient diagnosed with lipoma or multiple lipomas. 2. Patient with lipoma size having a diameter is less than 4cm. 3. Sites of lipoma Subcutaneous only. 4. Age group above 18 and below 60 years. 5. Patients willing for clinical trial. Irrespective of gender, occupation, religion, and economic barrier. 6. Patients with controlled DM and Hypertension.

Exclusion criteria

Exclusion criteria: 1.) Sites of lipoma Periosteal, Sub serosal, Submucosal (GI tract), Extradural (not intradural), Intra-articular, Sub- synovial, Sub-periosteal, Intraglandular breast, pancreas, kidney. If a patient develops any adverse effects which cause life-threatening conditions. 2.) Patients with other systemic diseases such as AIDS, HBsAg, TB, Uncontrolled Diabetes, Uncontrolled Hypertension, Malignancy, and Leprosy may affect the outcome of the Treatment. 3.) Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
The parameters will be noted down before and after treatment. 1.Size of swelling Timepoint: 14 Days study. 3 times per week for 2 weeks. 1st, 3rd, 5th, 7th, 9th, 11. final follow up on 21st day.

Secondary

MeasureTime frame
1) No improvement - 0 % relief in swelling. 2) Poor improvement - 0%-25% relief in swelling. 3) Mild improvement 26% to 50% relief in swelling. 4) Moderate improvement 51% to 75 % relief in swelling. 5) Marked improvement 76% to 100% relief in swelling. Timepoint: 14 Days study. 3 times per week for 2 weeks. 1st, 3rd, 5th, 7th, 9th, 11. Final follow-up on 21st day.

Countries

India

Contacts

Public ContactDr Aditya Thamdeo Fulzele

Dayabhai Maoji Majithiya Ayurved Mahavidyalaya ,Yavatma

drviharbidwai@gmail.com9822299174

Outcome results

None listed

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