Clinical Trial Findings

Dicon has proven itself in the laboratory as having a significant benefit for those suffering from Irritable Bowel Syndrome. In a placebo-controlled trial to test the efficacy of the remedy, patients suffering from IBS-constipation and IBS-diarrhea who took dicon showed measurable improvements and continued benefits even after cessation of the treatment.

“The clinical trial was administered by Dr. Warren Z. Jacobsohn, MD, Director of Institute of Gastroenterology (Ret.) in Shaare Zedek Hospital in Jerusalem, Israel. Dr. Jacobsohn was selected for his expertise in the field of gastroenterology and in particular for his experience with a myriad of patients exhibiting symptoms of IBS. The statistics were compiled and reviewed by Mario Baraz, leading statistician for Hadassah Ein Keren Hospital in Jerusalem.”

The participating patients were suffering from a range of typical IBS complaints such as constipation, diarrhea and pain-predominant IBS. Each of the test subjects was given a daily dose of either dicon or a placebo for a four-week period and the effects were monitored.

The results after the initial four weeks were dramatic among those taking the active ingredient with over 60% showing a considerable improvement in their condition. In particular, the sub-group of patients whose primary complaint was constipation (constipation-predominant) or mixed IBS showed the most pronounced reduction in symptom severity.

In conclusion the report found that there was a statistically significant benefit in taking dicon for those patients afflicted with IBS characterized by constipation. Patients suffering from IBS characterized by diarrhea were also shown to enjoy significant relief when using dicon, although in this condition a wider scale study was suggested due to the sample size.

Clinical Trial Data: IBS Constipation & Mixed

Description Of Test Used To Analyze Data