| CTRI Number |
CTRI/2025/11/097125 [Registered on: 10/11/2025] Trial Registered Prospectively |
| Last Modified On: |
17/02/2026 |
| Post Graduate Thesis |
No |
| Type of Trial |
Interventional |
|
Type of Study
|
Drug Ayurveda |
| Study Design |
Single Arm Study |
|
Public Title of Study
|
Checking if RSO Plus Oil is Safe and Works for People with skin infection |
|
Scientific Title of Study
|
An Open-Label, Single-Arm, Single-Center, Phase III Clinical Study to Evaluate the Safety and Efficacy of RSO Plus oil in Subjects with Cellulitis |
| Trial Acronym |
Nil |
Secondary IDs if Any
Modification(s)
|
| Secondary ID |
Identifier |
| CTSRS/2527 Version No. 3.0 Dated 13 Nov 2025 |
Protocol Number |
|
|
Details of Principal Investigator or overall Trial Coordinator (multi-center study)
|
| Name |
Dr Jamuna B A |
| Designation |
Principal Investigator |
| Affiliation |
RVS Ayurvedic Medical College Hospital and Research Centre |
| Address |
Ground Floor OPD-1, Srigandhadakavalu, Chandana Layout, Sunkadakatte, Bengaluru, Karnataka 560091
Bangalore KARNATAKA 560091 India |
| Phone |
6364898825 |
| Fax |
|
| Email |
drjamuna5289@gmail.com |
|
Details of Contact Person Scientific Query
|
| Name |
Ms Sathyavathi LM |
| Designation |
HOD-Clinical Operations |
| Affiliation |
Samahitha Research Solutions |
| Address |
Clinical Research Unit, No.1204, "Ashva", 2nd Floor, 26th Main, Jayanagar 9th Block, Bangalore
Bangalore KARNATAKA 560091 India |
| Phone |
09739001749 |
| Fax |
|
| Email |
satyalm@samahitha.com |
|
Details of Contact Person Public Query
|
| Name |
Ms Arpita Malgi |
| Designation |
Team Lead - Clinical Operations |
| Affiliation |
Samahitha Research Solutions |
| Address |
Clinical Research Unit, No.1204, "Ashva", 2nd Floor, 26th Main, Jayanagar 9th Block, Bangalore
Bangalore KARNATAKA 560069 India |
| Phone |
06364898825 |
| Fax |
|
| Email |
arpita@samahitha.com |
|
|
Source of Monetary or Material Support
|
| Teamworks United LLP 11-D, Sampat farms, Bicholi Mardana road,
Opp. Agarwal public school, Indore, Madhya Pradesh - 452016 |
|
|
Primary Sponsor
|
| Name |
Teamworks United LLP |
| Address |
11-D, Sampat farms, Bicholi Mardana road, Opp. Agarwal public school, Indore, Madhya Pradesh - 452016 |
| Type of Sponsor |
Pharmaceutical industry-Indian |
|
|
Details of Secondary Sponsor
|
|
|
Countries of Recruitment
|
India |
|
Sites of Study
|
| No of Sites = 1 |
| Name of Principal
Investigator |
Name of Site |
Site Address |
Phone/Fax/Email |
| Dr Jamuna B A |
RVS Ayurvedic Medical College, Hospital and Research Centre |
Ground Floor R.No-1, Srigandhadakavalu, Vishwaneedam Post, Outer Ring Road, Bangalore KARNATAKA |
06364898825
drjamuna5289@gmail.com |
|
Details of Ethics Committee
Modification(s)
|
| No of Ethics Committees= 1 |
| Name of Committee |
Approval Status |
| Pranav Diabetes Center Ethics Committee |
Approved |
|
|
Regulatory Clearance Status from DCGI
|
|
|
Health Condition / Problems Studied
|
| Health Type |
Condition |
| Patients |
(1) ICD-10 Condition:L039||Cellulitis and acute lymphangitis,unspecified. Ayurveda Condition: VISARPAH, |
|
|
Intervention / Comparator Agent
|
| sno | Intervention/Comparator | Type | Drug-Type | Procedure Name | Details | | 1 | Intervention Arm | Drug | Other than Classical | | (1) Medicine Name: RSO Plus Oil, Reference: NA, Route: Topical, Dosage Form: Taila, Dose: 2(ml), Frequency: od, Bhaishajya Kal: Adhobhakta, Duration: 40 Days, anupAna/sahapAna: No, Additional Information: -RSO Plus Oil 1-2ml applied topically once daily for 40 days
|
|
|
|
Inclusion Criteria
|
| Age From |
18.00 Year(s) |
| Age To |
50.00 Year(s) |
| Gender |
Female |
| Details |
1. Female participants aged 18–50 years.
2. Clinically diagnosed cellulitis of mild-to-moderate severity (as per investigator’s judgment).
3. No active dermatologic conditions or recent skin infections in the treatment area that could interfere with topical application.
4. Stable general health without chronic medical conditions requiring systemic therapy during the study period.
5. Willing and able to provide written informed consent prior to any study-related procedures.
6. Willing to comply with study requirements, including scheduled visits, questionnaires, and use of the investigational product as instructed. |
|
| ExclusionCriteria |
| Details |
1. History of skin allergy, eczema, or hypersensitivity in the treatment area.
2. Pregnant or breastfeeding women, or those planning pregnancy during the study period.
3. Known allergy or intolerance to any component of RSO Plus Oil.
4. Presence of severe cellulitis requiring immediate systemic antibiotic therapy or hospitalization.
5. Participation in another clinical study or use of investigational drugs within the last 30 days prior to screening.
6. Current use of other topical medicated/herbal treatments on the affected area.
7. Any condition that, in the opinion of the investigator, may compromise subject safety, compliance, or study integrity. |
|
|
Method of Generating Random Sequence
|
Not Applicable |
|
Method of Concealment
|
Not Applicable |
|
Blinding/Masking
|
Open Label |
|
Primary Outcome
|
| Outcome |
TimePoints |
1. Change in incidence and severity of cellulitis symptoms (erythema, skin irritation, burning sensation, hypersensitivity) from baseline to Day 20 and Day 40.
-Assessment tools:
a. Physician’s global assessment (clinical grading scale: none, mild, moderate, severe).
b. Patient-reported symptom severity using Visual Analog Scale (VAS; 0–10 cm).
-Endpoint definition: Mean change in composite symptom scores compared to baseline. |
Screening / Baseline (Day 0)
Visit 2 (Day 20 ±2)
Visit 3 (Day 40 ±2; EOS) |
|
Secondary Outcome
Modification(s)
|
| Outcome |
TimePoints |
1. Improvement in cellulite grade & skin firmness/texture
- Measured using the Cellulite Severity Scale (CSS), a validated 5-item scale (range 0–15).
- Evaluated at baseline, Day 20, & Day 40.
2. Improvement in quality of life (QoL)
- Assessed using the Dermatology Life Quality Index (DLQI) or equivalent validated dermatology-specific questionnaire.
- Mean change from baseline to Day 20 & Day 40.
3. Subject satisfaction & cosmetic acceptability
- Measured through a structured questionnaire rating texture, smoothness, fragrance, & overall product satisfaction (5-point Likert scale).
4. Safety & tolerability
- Incidence, severity, & causality of adverse events (AEs) & adverse drug reactions (ADRs).
- Changes in vital signs (Baseline & Day 40). |
Screening / Baseline (Day 0)
Visit 2 (Day 20 ±2)
Visit 3 (Day 40 ±2; EOS) |
|
|
Target Sample Size
|
Total Sample Size="20" Sample Size from India="20"
Final Enrollment numbers achieved (Total)= "20"
Final Enrollment numbers achieved (India)="20" |
|
Phase of Trial
|
Phase 3 |
|
Date of First Enrollment (India)
|
18/11/2025 |
| Date of Study Completion (India) |
08/01/2026 |
| Date of First Enrollment (Global) |
Date Missing |
| Date of Study Completion (Global) |
Date Missing |
|
Estimated Duration of Trial
|
Years="0" Months="6" Days="0" |
Recruitment Status of Trial (Global)
Modification(s)
|
Not Applicable |
| Recruitment Status of Trial (India) |
Completed |
|
Publication Details
|
N/A |
|
Individual Participant Data (IPD) Sharing Statement
|
Will individual participant data (IPD) be shared publicly (including data dictionaries)?
Response - NO
|
Brief Summary
Modification(s)
|
Brief Summary Cellulitis is a common bacterial infection of the skin and subcutaneous tissue, characterized by redness, swelling, warmth, and tenderness. Despite standard antibiotic therapy, recurrence and incomplete resolution of local symptoms remain frequent due to persistent inflammation and impaired skin barrier recovery. RSO Plus Oil is a proprietary Ayurvedic formulation containing herbal oils with anti-inflammatory, antimicrobial, antioxidant, and wound-healing properties. The formulation is intended for topical use to alleviate local symptoms, promote healing, and enhance quality of life in patients with cellulitis. This open-label, single-arm, single-center clinical study aims to evaluate the efficacy, safety, and tolerability of RSO Plus Oil applied topically once daily for 40 days in adult female subjects with mild-to-moderate cellulitis. The primary endpoint is the reduction in erythema, swelling, burning sensation, and hypersensitivity from baseline to end of treatment. Secondary objectives include improvement in skin texture and firmness, quality of life, and subject satisfaction. Results: This Phase III, open-label, single-arm clinical study demonstrated that topical application of RSO Plus Oil resulted in clinically meaningful improvement in adult female subjects with mild-tomoderate cellulitis over a 40-day treatment period. Statistically and clinically relevant reductions were observed in both physician-assessed and patient-reported local symptoms of cellulitis, including erythema, skin irritation, burning sensation, and hypersensitivity, indicating effective local symptom control. The study also shows effect of RSO Plus Oil on subcutaneous fat deposits. Progressive reductions in extra fat deposited under the skin were observed across multiple body regions, including the abdomen, thighs, hips, arms, and neck, along with visible improvements in skin appearance. Consistent improvements were noted across secondary efficacy endpoints. Cellulite severity and skin texture/firmness demonstrated progressive improvement as assessed by the Cellulite Severity Scale (CSS). Quality of life, measured using the Dermatology Life Quality Index (DLQI), showed improvement across all domains, reflecting reductions in physical discomfort, emotional distress, and interference with daily activities and social functioning. Subject satisfaction and cosmetic acceptability assessments further supported favourable user experience and perceived therapeutic benefit. RSO Plus Oil was well tolerated throughout the study. No serious adverse events were reported. All adverse events were mild, transient, resolved without medical intervention, and were assessed as unrelated to the investigational product. High treatment compliance further supported the feasibility and acceptability of daily topical application. In conclusion, RSO Plus Oil demonstrated a favourable safety profile and clinically meaningful efficacy in reducing local cellulitis symptoms, improving cellulite severity and skin quality, and reducing subcutaneous fat deposits across multiple body areas. These findings support its potential role as a safe and effective adjunctive topical therapy |