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Effect of a Yogic Breathing Technique on Mouth Lesions in Tobacco Users

Effect of Sequential Mindful Breathing (Ojas Breath) on Capillary Blood Uric Acid Levels and clinical response in Patients with Oral Leukoplakia Receiving Curcumin Supplementation: An 8 Week Clinical Study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/106066
Enrollment
80
Registered
2026-03-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: T758- Other specified effects of external causes

Interventions

Intervention1: 1.Sequential Mindful Breathing (Ojas Breath) 2.Standardized Tobacco Cessation Counseling 3. Curcumin Supplementation: 1. Sequential Mindful Breathing (Ojas Breath) Protocol This stru

Sponsors

DrPKMeena priya
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Participants meeting all of the following criteria will be included: Adults aged 18 60 years. Clinically diagnosed cases of oral leukoplakia based on standard clinical criteria. Presence of measurable lesion(s) suitable for dimensional assessment. Willingness to undergo curcumin supplementation and tobacco cessation counseling. Willingness to learn and practice Sequential Mindful Breathing (Ojas Breath) (for study group participants). Ability to provide written informed consent.

Exclusion criteria

Exclusion criteria: Participants meeting any of the following criteria will be excluded: Use of antioxidant supplements or herbal antioxidant therapy within the past 1 month. Presence of systemic diseases known to significantly influence oxidative stress or uric acid metabolism (e.g., uncontrolled diabetes mellitus, chronic kidney disease, gout). Current use of medications affecting uric acid levels (e.g., allopurinol, febuxostat, thiazide diuretics). History of malignancy or clinically suspected malignant transformation of the lesion. Pregnancy or lactation. Ongoing participation in another clinical trial. Inability to comply with the 8-week follow-up schedule. Physical or cognitive limitations that prevent proper performance of the breathing protocol.

Design outcomes

Primary

MeasureTime frame
Mean change in capillary blood uric acid level from baseline to 8 weeks, compared between the study and control groups.Timepoint: Mean change in capillary blood uric acid level from baseline to 8 weeks, compared between the study and control groups.

Secondary

MeasureTime frame
1.Mean change in lesion area from baseline to Week 8. 2.Proportion of participants achieving CR or PR at Week 8.Timepoint: Clinical lesion measurements will be recorded at baseline, Week 4, and Week 8, with final response classification performed at Week 8.

Countries

India

Contacts

Public ContactDrPKMeena priya

JKKN Dental College

meenapriya@jkkn.ac.in09865248844

Outcome results

None listed

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