CTRI/2018/10/016065CompletedPhase 3
A Comparative Effectiveness Study of 50 Millesimal Potencies and Centesimal Potencies in the Treatment of Tinea Corporis: An Open, Randomized, Pragmatic Trial
DNDe Homoeopathic Medical College and Hospital0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Diagnosed case of Tinea corporis, suffering for at least 3 months (ICD 10 B35.4)
- •2. Age 18-65 yrs
- •3. Both sexes
- •4. Literate patients who are able to read or write
- •5. Patient using topical agents for tinea lesions will be included after a washout period of two weeks
Exclusion Criteria
- •1. Cases with complications like lichenification and eczematisation
- •2. Similar looking skin conditions; e.g. seborrhic dermatitis, pityriasis rosea and some types of psoriasis
- •3. Patients who are too sick for consultation, unable to read patient information sheet, unwilling to take part or not giving consent to join the study
- •4. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure
- •5. Pregnant women and lactating mothers
- •6. Substance abuse and/or dependence
- •7. Self-reported immune-compromised state, and
- •8. Already undergoing homeopathic treatment for chronic disease within last 6 months
Investigators
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