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Oral Cancer Biomarker Study

Validation of the Beta Defensin Index (BDI) as a Biomarker for Oral Cancer in India - Hbd

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/01/017092
Enrollment
60
Registered
2019-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: C069- Malignant neoplasm of mouth, unspecified

Interventions

Intervention1: NIL: NIL

Sponsors

Case Western Reserve university
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Consent â?? Subjects must demonstrate understanding of the study procedures as evidenced by voluntary written informed consent and has received a copy of the consent form. 2. Compliance â?? Subjects must be willing, able, and likely to comply with all study procedures and restrictions. 3. Age â?? Subjects must be 18 years of age or older. There are no restrictions on maximum age. 4. Diagnosis â?? Subjects must be currently undergoing clinical evaluation for determination of OSCC diagnosis due to the presence of suspicious red or white lesions, with no prior history of HNC Lesions >5mm that fill the following requirements: i. Include non-diagnosed yet suspicious lesions of the subsites above like CIS, T1 and T2 lesions. ii. Include diagnosed premalignant and early malignant lesions (again CIS, T1 and T2 lesions). iv. Include superficial lesions like Leukoplakia, Erythroplakia and deeper but common problems. v. Exclude large Necrotic lesions (clinically advanced cancer T3 and T4) either diagnosed or non-diagnosed cancers in this group as often as possible

Exclusion criteria

Exclusion criteria: 1. Very small Lesions Less than 5 mm in size. 2. T1, T2 Lesions with Necrotic areas. 3. Diagnosis â?? Individuals with Prior diagnosis of any head neck malignancy. 4. Patients with previous or current treatment involving radiation and/or chemotherapy, regardless of cancer type or cancer diagnosis dates, will be excluded. 5. Pregnancy 6. Anything that would place the individual at increased risk or preclude the individualâ??s full compliance with or completion of the study.

Design outcomes

Primary

MeasureTime frame
Evaluation of Human Beta defensin Level in normal mucosa as well as cases of oral cancerTimepoint: 1month from sample collection

Secondary

MeasureTime frame
correlation Human beta defensin index 2, 3 with histopathology reportTimepoint: after final histopathology report

Countries

India

Contacts

Public ContactDr Deepa Nair

Tata Memorial Centre, Mumbai.

drdeepanair@hotmail.com

Outcome results

None listed

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