Figure 1.

The schematic diagram of current clinical study. The study enrolled “intension to treat” 40 subjects through the inclusion and exclusion criteria screening followed by the SAS random number generation method. Upon discontinuation of one subject from each group, total 38 subjects were considered per protocol for evaluation. No subject reported for adverse events or serious adverse events. The study compliance was checked at every follow-up visit alongside study evaluation and assessment by a team of physician-investigator and officers.