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Laser Acupuncture for Smokeless Tobacco Cessation

EFFICACY OF AURICULAR LASER ACUPUNCTURE AND BEHAVIOURAL COUNSELING IN REDUCING NICOTINE DEPENDENCE AMONG DENTAL PATIENTS USING SMOKELESS TOBACCO - A RANDOMIZED CONTROLLED TRIAL - LASC

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/07/044503
Enrollment
102
Registered
2022-07-29
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: K137- Other and unspecified lesions of oral mucosa

Interventions

Intervention1: Auricular laser acupuncture for reducing nicotine dependence related to smokeless tobacco use: Diode laser equipment (Novolase, Novolase Technologies, India) with a power output of 100

Sponsors

Dr Mahalaxmi HS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy adults aged 18- 35years, willing to quit smokeless tobacco use and who report to peripheral center of Bapuji Dental College and Hospital, at Community Health center, Malebennur. 2. Adults using smokeless tobacco along with pan masala (vimal, G S T, siddhu) and gutka (star, RMD, pan parag). 3. Adults who have not undergone nicotine replacement, behavioral or pharmacotherapy for tobacco cessation in their life time. 4. Adults whose salivary thiocyanate level will be more than 2mMol/ml of saliva (objective criteria for determining tobacco exposure)

Exclusion criteria

Exclusion criteria: 1. Adults with history of smoking and/or other substance use like heroin, marijuana, cannabis, benzodiazepines, opioids 2. Adults diagnosed with oral submucosal fibrosis, leucoplakia, tobacco-associated keratosis and any type of oral malignancy 3. Adults under medication which may affect their salivary flow rate. 4. Pregnant and lactating women 5. Adults with infection at and around the acupoints and/ or lack skin sensation near the acupoints 6. Adults unable to comply with appointment schedule

Design outcomes

Primary

MeasureTime frame
Nicotine Dependence Level (Fagerstrom Test Scores)Timepoint: Baseline and one month post intervention

Secondary

MeasureTime frame
Salivary Thiocyanate level,Withdrawal effects assessed on 10 point Visual Analog scaleTimepoint: 1 month post intervention

Countries

India

Contacts

Public ContactDR Mahalaxmi HS

Bapuji Dental College and Hospital,Davanagere

pujacyavagal@gmail.com9972946664

Outcome results

None listed

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