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Trial Data

OptiLiv®

(Hepatogenic, Hepato-protective and Hepatic Stimulant : Capsules and Syrup)

This Product is available in Ukraine under the name GEPATOVID Capsule & Syrup

In a randomized placebo controlled double blind trial, 62 patients of pulmonary TB were given either OptiLiv or placebo during the first 45 days of intensive phase ATT. In addition, 8 patients already on ATT having drug induced jaundice were also randomized and added to the above schedule of study in a dose of one capsule twice a day but without any ATT. Changes in Serum Bilirubin, SGOT, SGPT and Alkaline Phosphatase were negligible in OptiLiv supplemented groups, as compared to the placebo group. Further, a significant rise in hemoglobin was also seen in the OptiLiv treated group. In cases with established jaundice due to ATT, faster recovery was seen in patients on OptiLiv treatment. With OPTILIV all patients had marked feeling of well-being, improved appetite and weight gain and their bowel movements became regular with well formed stools.

This study thus brings forth clearly the benefit of adding OptiLiv capsules as an integral part of intensive phase ATT in order to prevent overt and incipient hepatotoxicity and thus minimize the chances of treatment default and discontinuation, which is a common cause for development of resistance to standard ATT.

Singh, V.K. (2000), J.K. Practitioner (2000), 7 (4) : 289-292).

Forty adult patients of either sex and between 14 to 50 years of age suffering from acute viral hepatitis were randomized. OptiLiv capsules or placebo were given in 1 capsule b.d. dose for 15 days. Treatment with OptiLiv was associated with significantly less (P<0.05) loss in body weight and rapid (P<0.05) clinical and bio-chemical recovery, as compared to placebo. No relapse was observed in OptiLiv group.

Biswas, et al (1998), AIIMS, New Delhi, Paper was presented at XIIIthinternational Congress of Pharmacology, 26-31 July, 1998, Munchen, Germany.

Clinical Trial of OptiLiv was conducted in healthy male volunteers (age 20-40 years) as per the terms of Helsinki declaration. Safety and tolerability of the formulation was well established with no adverse effect on clinical or biochemical parameters. Improvement was seen in hepatic and renal function values as they declined to the lower limits of normal, from the higher range thereby signifying improved and efficient hepatic and renal function. This was reflected in improvement of subjective parameters in a majority of the volunteers who reported better appetite and bowel evacuation. Significant anti-hypercholesterolaemic effect was noted in individuals in whom Serum cholesterol values were > 220 mg. These effects along with the high safety and tolerability profile of OptiLiv coupled with its convenient dosage schedule make it an ideal herbal Hepatoprotective, Hepatogenic and Hepatic tonic for use in liver dysfunction of varied aetiology.

Mathur, AK et. al.(1998). Paper presented at Annual APPI Conference, Imphal, Dec'98.

 

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