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Department of Obstetrics, Gynecology & Reproductive Sciences
Clinical Trials
Clinical Research is conducted at Fletcher Allen Health Care (FAHC), including the General Clinical Research Center (GCRC), and includes original investigations initiated by faculty as well as participation in national Phase III trials. Techniques used include the following: Color Doppler ultrasonography, DEXA scans, abdominal CT scans, euglycemic clamps, activity surveys, laparoscopic ovarian diathermy.
If you would like additional information, or to inquire about participating in an ongoing study, please contact:
Penny Fairhurst, RN, CCRC
Clinical Research Coordinator
Phone: (802) 656-7505
E-Mail: Penny.Fairhurst@vtmednet.org
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Study Title: Pre-pregnancy Phenotype and Predisposition to Preeclampsia
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| Purpose: The goal of this research is to examine the contribution of prepregnancy physiologic phenotype to the development of preeclampsia. In addition, we are looking to understand the influence of pregnancy-specific, physiologic adaptations to the pathophysiologic associations of preeclampsia in a group of women at risk for developing preeclampsia. Currently recruiting women who are planning to become pregnant within the next year. |
| Primary/Site/Co Investigator: Ira Bernstein, M.D. |
| Contact: Carole McBride |
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Study Title: Water Birth Registry
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| Purpose: All water births at FAHC are being reviewed and added to a database. This will document outcomes and complications. |
| Primary/Site/Co Investigator: Eleanor Capeless, M.D. |
| Contact: Eleanor Capeless |
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Study Title: The Impact of Structured Pelvic Floor Physical Therapy on Sexual Functioning and Urinary Incontinence Scores in Women with Sexual Dysfunction and Lower Genitourinary Symptoms
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| Purpose: Studies confirm improvements in both urinary incontinence (UI) and pelvic organ prolapse (POP) when treatments incorporate pelvic floor physical therapy (PFPT). A higher incidence of sexual dysfunction has been identified in women with lower urinary tract symptoms, such as UI or POP. The aim of this study was to determine if a supervised PFPT program improves sexual function in women reporting sexual dysfunction and lower urinary/genital tract symptoms, using two established validated questionnaires. |
| Primary/Site/Co Investigator: Julia LaCombe, M.D. |
| Contact: Julie LaCombe |
Last modified January 15 2013 01:08 PM
