Homeopathic treatment of muscle pain

INTERVENTION: Intervention1: Individualized homoeopathic medicines in individualized dosage in centesimal potencies plus concomitant care: The proposed intervention entails the administration of prescribed homoeopathic medications at centesimal potencies (CH). Every dosage consists of four No. 40 cane sugar globules moistened with the prescribed medication (kept in 90% v/v ethanol), which is to be taken orally on an empty stomach with a clean tongue. The dosage and frequency of administration depend on the specific needs of each case. Patients will be instructed to suck the globules rather than swallow them, and they will be forbidden from handling the globules or from eating, drinking, smoking, or brushing their teeth for 30 minutes after ingesting them. Every time, a single, customized medication will be recommended, taking into consideration the entirety of the patients presenting symptoms, the clinical history, the patients constitutional characteristics, any miasmatic expressions, and when necessary, repertorization utilizing ZOMEO software. concomitant care measures include gentle physical aerobic and strength training exercises .Route of Administration : per oral. Duration of follow up:3 months. Control Intervention1: Identical looking placebo plus concomitant care: This arm will be given a placebo that looks exactly like verum. Each dose of the placebo will consist of four (number forty) cane sugar globules, moistened with rectified spirit, to be taken orally on an empty stomach and clean tongue; the dosage and repetition depend on the specific needs of each patient management guidelines will be given as in the experimental arm.The therapy lasted for three months. The medications and placebos will be repackaged in matching glass bottles, labeled with the medications name, po CONDITION: Health Condition 1: M797‐ Fibromyalgia PRIMARY OUTCOME: The Revised Fibromyalgia Impact Questionnaire (FIQR)Timepoint: Baseline, and every month, up to 3 months SECONDARY OUTCOME: Measure yourself Medical Outcome Profile v‐2 (MYMOP‐2) questionnaireTimepoint: Baseline, and every month, up to 3 months Multi Dimensional questionnaire for patient reported outcome measures ‐ Fibromyalgia (PROM FM)Timepoint: Baseline, and every month, up to 3 months INCLUSION CRITERIA: 1.Patients who have received a diagnosis of primary fibromyalgia according to The American College of Rheumatology 2010 criteria for the classification of fibromyalgia ? Widespread pain score 7 or more ? Based on severity of symptom (SS 5 or more) 2. Age between 18 and 65 years 3. Symptoms are present for at least 3 months. 4. Participants of either se Xor transgender. 5. Patients ability to understand English / Hindi / Bengali