tility of individualized homoeopathic medicine in management of pain in cases of paronychia: a prospective open label observational clinical study

DG CCRH0 个研究点目标入组 0 人开始时间: 待定最近更新: 2024年5月27日

试验速览

暂无简介。

•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.

•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.

发起方

DG CCRH