Eligibility
Ages eligible for study: 10-40 years, genders eligible for study: Both inclusion and exclusion criteria. Informed consent from the patients.
Design
Case control direct, unicentre, prospective, randomized authentic allopathic controlled, two arm parallel group clinical trial.
Ages eligible for study: 10-40 years, genders eligible for study: Both inclusion and exclusion criteria. Informed consent from the patients.
Design
Case control direct, unicentre, prospective, randomized authentic allopathic controlled, two arm parallel group clinical trial.
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