To study the effects of homoeopathic treatment in reduction of smokeless tobacco.
- Conditions
- Health Condition 1: F172- Nicotine dependence
- Registration Number
- CTRI/2023/06/054183
- Lead Sponsor
- oble Homoeopathic College and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. New cases diagnosed on the basis of diagnostic criteria and pre diagnosed cases of smokeless tobacco.
2. Patients willing to participate in the study and giving written informed consent.
3. Only those patients will be considering into the study that have consumption of smokeless tobacco for last 1 year or more.
4. Currently and continuous uses of smokeless tobacco.
1. Cases with any type of oral pathology.
2. Patients with other systemic diseases.
3. Patients having mental and behaviour disorder due to psycho active substance other than tobacco.
4. Patient is already under going nicotine replacement therapy.
5. Patient already undergoing homoeopathic treatment for any chronic disease.
6. Any symptoms suggestive of any serious medical condition that may require active intervention within 6 months.
7. Pregnant women and lactating mothers.
8. Patients not giving written consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess changes in the FTND-ST through individualized homoeopathic treatment.Timepoint: Baseline, 4 weeks, 8 weeks, 12 weeks, till 6th month.
- Secondary Outcome Measures
Name Time Method To shortlist the commonly indicated homoeopathic medicines.Timepoint: Baseline, 4 weeks, 8 weeks, 12 weeks, till 6th month.