![]() ![]() Group 1: 25mm +/- 27mm (standard deviation).They enrolled 120 patients over a 6 month period, and 113 completed the protocol. A 13 mm (out of 100) difference was considered clinically significant. The primary outcome was relief of pain (as measured by the difference in millimeters between the pretreatment and posttreatment visual analog scales) at 30 minutes. Group 3: 30 mL of Mylanta plus 10mL of Donnatal plus 10 mL of 2% viscous lidocaine Outcome ![]() Group 2: 30 mL of Mylanta plus 10mL of Donnatal (a combination of phenobarbital, hyoscyamine sulfate, atropine sulfate, and scopolamine hydrobromide, meant to act as an antispasmodic and anticholinergic agent) Group 1: 30 mL of Mylanta (a combination of magnesium hydroxide, aluminium hydroxide, and simethicone)
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