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Through the use of a doule blind technique, the drug, Solantal, was tested against a control group in order to investigate the extent of its therapeutic effects on patients having recieve an episiotomy and at Laparoscopic sterilization as well as on patients with chronic P. I. D. and pelvic Congestion Symdrome. The results were as follows : In both the Yoon`s Ring method and the electro-cautery method of Laparoscopic sterilization, excellent results were found in 10% of the (Pontal) control group and in 27% of the Solantal group. In mother having received an episiotomy; excellent results were seen in only 12% of the control group cases, whereas, using either 300mg or 600mg of Solantal, excellent results could be seen in 44% of the cases. There was no significant difference in the therapeutic effect between the 300 mg per day and the 600mg per day Solantal groups when the drug was used on episiotomy or laparoscopic sterilization patient groups. There were no dermatologic complications following the administration of Solantal for laparoscopic sterilization or for episiotomy. In those patients tested having chronic P.I.D. and the pelvic Congestion Syndrome, 14% showed excellent results, 42% good results, 28% fair to poor results and 17% showed no effectiveness at all. There were no hypersensitive or other adverse side effects noted in any of the cases studied.
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