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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  
Name  Address 
NIL  Nil 
 
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  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition:L039||Cellulitis and acute lymphangitis,unspecified. Ayurveda Condition: VISARPAH,  
 
Intervention / Comparator Agent  
snoIntervention/ComparatorTypeDrug-TypeProcedure NameDetails
1Intervention ArmDrugOther 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

 
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