Homoeopathy in paronychia
Not Applicable
Completed
- Conditions
- Health Condition 1: L030- Cellulitis and acute lymphangitisof finger and toe
- Registration Number
- CTRI/2019/06/019563
- Lead Sponsor
- DG CCRH
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Age 18-60 years
2. Both sexes
3. Clinically diagnosed cases of paronychia in one or more fingers or toes.
4. Patients already undergoing regular oral or topical analgesics or NSAID therapy for painful episodes of paronychia provided the medications are stopped completely at least 2 weeks prior study entry.
5. Providing written informed consent to take part in the study.
Exclusion Criteria
1. Patient suffering from nail diseases other than paronychia.
2. Patient taking NSAIDS or using topical application within 2 weeks of recruitment into the study, or undergoing homeopathic treatment for any chronic disease within last 1 month.
3. Unwilling to take part and not giving consent to join the study.
4. Self-reported immune-compromised state.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. NRS pain rating score estimation.Timepoint: 1. NRS pain rating score estimation at baseline and after 2 months.
- Secondary Outcome Measures
Name Time Method 1. DLQI scale and Modified naranjo criteria assessment.Timepoint: After 2 months of treatment