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NCT ID: NCT00941590 Not yet recruiting - Clinical trials for Central European Encephalitis

Postencephalitic Symptoms After Tick Borne Encephalitis

Start date: July 2009
Phase: N/A
Study type: Observational

The purpose of this study is to assess clinical outcome in patients with tick borne encephalitis.

NCT ID: NCT00548288 Not yet recruiting - Arthroplasty Clinical Trials

Effect of Local Pamidronate in Preventing Bone Loss After Total Hip Arthroplasty

Start date: November 2007
Phase: Phase 1
Study type: Interventional

The aims of the study are to determine whether pamidronate applied locally causes diminished periprosthetic bone loss and decreased rate of bone turnover compared to patients receiving placebo after cemented total hip arthroplasty (THA). The study design will be prospective, randomized, and blind. Periprosthetic bone mineral density (BMD) will be measured with dual energy X-ray absorptiometry (DXA) at the total periprosthetic area as well as at seven Gruen zones or regions of interest. DXA scans will be performed at one week (baseline), three months, and six months postoperatively. Mean values of biochemical markers of bone turnover, BMD, and baseline-normalized BMD values will be compared between the bisphosphonate and placebo groups at each time point. For all temporal measurements including bone markers, BMD and normalized BMD, mean values will be compared across each time point within a given group.