Desmostachya Bipinnata Platinum Patch for Oral Ulcers in Cancer Therapy
- Conditions
- Malignant neoplasm of mouth, unspecified,
- Registration Number
- CTRI/2025/04/084509
- Lead Sponsor
- Department of Health Research
- Brief Summary
We are conducting this study to develop an **effective, plant-based nanomedicine** for managing **chemotherapy-induced oral mucositis**, a painful and debilitating condition that significantly impacts cancer patients’ **quality of life, nutrition, and treatment adherence**. Current treatments provide **limited relief** and often have **side effects**, necessitating **a safer, more effective alternative**. The **Db platinum mucoadhesive patch** integrates **Desmostachya bipinnata-derived phytochemicals with platinum nanoparticles**, offering **anti-inflammatory, wound-healing, and antimicrobial properties**. This study aims to assess its **efficacy in reducing mucositis severity, pain, and microbial load**, while improving **oral healing and patient comfort**, ultimately enhancing **clinical outcomes in cancer care**.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 30
- Patients aged 30 years and above, diagnosed with oral squamous cell carcinoma (OSCC) and operated for the same.
- Undergoing chemotherapy post-surgery and at risk of developing oral mucositis.
- Willing to participate and provide informed consent.
- No known allergies to the Db platinum mucoadhesive patch components.
- Patients with severe (Grade 4) oral mucositis at baseline.
- History of severe allergic reactions to herbal or nanoparticle-based formulations.
- Presence of active oral infections (bacterial, viral, or fungal).
- Pregnant or lactating women or those with severe systemic illnesses.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduction in Oral Mucositis Severity The follow-up schedule includes assessments at Day 0 (baseline), Day 3 (early pain reduction and safety check), Day 7 (mucositis improvement and compliance check), Day 14 (final mucositis grading and microbial analysis), Day 21 (extended healing evaluation if needed), and Day 30 (long-term QoL assessment). These timepoints provide a comprehensive evaluation of the therapeutic efficacy, safety, and patient adherence to the Db platinum mucoadhesive patch Measured using the World Health Organization (WHO) Oral Mucositis Grading Scale or National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE). The follow-up schedule includes assessments at Day 0 (baseline), Day 3 (early pain reduction and safety check), Day 7 (mucositis improvement and compliance check), Day 14 (final mucositis grading and microbial analysis), Day 21 (extended healing evaluation if needed), and Day 30 (long-term QoL assessment). These timepoints provide a comprehensive evaluation of the therapeutic efficacy, safety, and patient adherence to the Db platinum mucoadhesive patch Assessed by the reduction in ulcer size, severity of pain, and ability to eat/drink The follow-up schedule includes assessments at Day 0 (baseline), Day 3 (early pain reduction and safety check), Day 7 (mucositis improvement and compliance check), Day 14 (final mucositis grading and microbial analysis), Day 21 (extended healing evaluation if needed), and Day 30 (long-term QoL assessment). These timepoints provide a comprehensive evaluation of the therapeutic efficacy, safety, and patient adherence to the Db platinum mucoadhesive patch
- Secondary Outcome Measures
Name Time Method Pain Reduction Assessed using the Visual Analog Scale (VAS) (0 = no pain, 10 = worst pain).
Trial Locations
- Locations (1)
SAVEETHA DENTAL COLLEGE & HOPSITALS
🇮🇳Chennai, TAMIL NADU, India
SAVEETHA DENTAL COLLEGE & HOPSITALS🇮🇳Chennai, TAMIL NADU, IndiaDr Nitya KrishnasamyPrincipal investigator09962623510drknitya@gmail.com