02140nas a2200349 4500000000100000008004100001260001700042653001500059653001000074653002600084653001000110653002200120653001100142653001100153653002300164653001200187653000900199653001600208653001400224653001300238653002200251100001700273700001500290700001700305700001700322245012200339300001100461490000700472050001800479520127900497022001401776 2003 d c2003 Jul-Sep10aAdolescent10aAdult10aAnti-Bacterial Agents10aChild10aDrug Combinations10aFemale10aHumans10aLeprostatic Agents10aleprosy10aMale10aMinocycline10aOfloxacin10aRifampin10aTreatment Outcome1 aDeshmukh A R1 aDhurat R S1 aJerajani H R1 aJerajani U R00aA comparative clinico-pathological study of single dose ROM in paucibacillary leprosy patients with 1-3 skin lesions. a209-170 v75 aDESHMUKH 20033 a
A controlled clinical and histopathological study was carried out to compare the efficacy of a combination of rifampicin 600 mg plus ofloxacin 400 mg plus minocycline 100 mg (ROM) administered as a single dose with that of standard WHO/MDT-PB six months' regimen with regard to resolution of lesion clinically and histopathologically. Skin biopsy was performed at the intake and at 6 months. The study subjects were 32 previously untreated, smear-negative patients, without nerve trunk involvement and having 1-3 skin lesions. The results were analyzed for mean clinical score for marked, moderate and no improvement and mean histopathological score was graded as active, resolving and complete resolution, according to granuloma fraction at the end of 6 months. Marked clinical improvement was seen in 25% and 12%, moderate improvement in 50% and 56% patients treated with ROM and standard regimens respectively. Histopathologically, activity was seen in 62.5% and 43.7% and resolution of granuloma in 25% and 31.2% in the ROM and standard regimens respectively. Both the regimens were equally efficacious in the reduction of clinical score and granuloma fraction. No adverse drug reactions or reversal reactions were seen during the study period in both the groups.
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