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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT00420264 |
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Date of registration:
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10/01/2007 |
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Primary sponsor: |
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Public title:
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ThermaChoice III Under Local Sedation in the Office Setting
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Scientific title:
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Feasibility of Using Gynecare Thermachoice III in the Office Setting Without Conscious Sedation |
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Date of first enrolment:
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November 2005 |
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Target sample size:
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20 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT00420264 |
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Study type:
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Observational |
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Study design:
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Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal, Time Perspective: Prospective
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Countries of recruitment
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United States
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Contacts
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Name:
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Douglas M Van Drie, MD |
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Address:
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Telephone:
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616-774-0700 |
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Email:
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vandriedm@gvgobgyn.com |
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Affiliation:
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Name:
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Jason B Bennett, MD |
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Address:
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Telephone:
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616-774-0700 |
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Email:
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bennettjb@gvgobgyn.com |
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Affiliation:
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Name:
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Jason B Bennett, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Grand Valley Gynecologists, PC |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Heavy uterine bleeding
Exclusion Criteria:
- Uterine or cervical cancer
- Unable to tolerate office hysteroscopy
- Uterine fibroid tumors that distort endometrial cavity
- Uterine cavity greater than 12 cm
- Patients with hyperplasia or premalignant changes of the endometrium
- Active genital or urinary tract infections
- Intrauterine device
- Pregnant or want to become pregnant
Age minimum:
30 Years
Age maximum:
60 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Heavy Uterine Bleeding
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Secondary ID(s)
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ThermaChoice III
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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