ARTHRICEPT CLINICAL FIELD STUDY SUMMARY
A clinical field study using a combination application of the Arthricept oral and topical products was evaluated in 33 compromised volunteers with multiple joint problems and pain ailments. The Arthricept topical and oral combination regimen provided significant benefit with greater than 80% success ratewithin the first month of use. At the end of the three month trial period 25 participants were completely pain free and an additional 5 were pain free in daily life but experience minimal residual pain during and after strenuous tasks.
At start of the field study, the daily life of each volunteer was significantly impacted by regular chronic pain and in many cases continuous pain. All were suffering with chronic pain in more than one joint for a minimum of six months. All volunteers had significantly compromised range of motion. Some had pain for many years. Ages ranged from 25 to 68 years with median age of 58 years. All were taking pain medications. All volunteers have tried or were using multiple standard or alternate treatments with minimal or no benefit and were not helped by these therapies.
At the end of three month trial period 25 volunteers were completely pain free and were able to complete many strenuous tasks that they could not do earlier additional 5 had minimal pain at times with strenuous tasks. All 30 had significantly improved range of motion. Only three of the 33 volunteers reported no benefit.
In this limited sampling of volunteer use, no prolonged side effects were reported. All their daily function remained normal except for few who reported loose bowl movement for the initial three to four days at start of treatment that returned to normal after initial deviation. All reported greater freedom and significant improvement in quality of life. Many reported sound and uninterrupted sleep. Poor sleep was a chronic problem for this group.
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