Endocervical Evaluation With the Curette Versus Cytobrush for the Diagnosis of Dysplasia of the Uterine Cervix
NCT ID: NCT01435590
Last Updated: 2015-05-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
180 participants
INTERVENTIONAL
2011-09-30
2014-09-30
Brief Summary
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METHOD: women referred to colposcopy because of abnormal Papanicolaou tests will be randomized to endocervical sampling with either a metal curette (endocervical curettage -ECC) or and endocervical brush. All samples will be submitted for histological study.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Interventions
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Curette v/s endocervical brush
Eligibility Criteria
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Inclusion Criteria
* 21 years or older
* Attending our colposcopy clinic
* Need for endocervical evaluation
* Full autonomy or capacity to understand the procedures
Exclusion Criteria
* Absence of uterus
* History of DES exposure in utero
21 Years
70 Years
FEMALE
No
Sponsors
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University Hospital, Geneva
OTHER
Responsible Party
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Manuela Undurraga Malinverno
Medecin Interne
References
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Undurraga M, Catarino R, Navarria I, Ibrahim Y, Puget E, Royannez Drevard I, Pache JC, Tille JC, Petignat P. User perception of endocervical sampling: A randomized comparison of endocervical evaluation with the curette vs cytobrush. PLoS One. 2017 Nov 6;12(11):e0186812. doi: 10.1371/journal.pone.0186812. eCollection 2017.
Other Identifiers
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CER 11-029
Identifier Type: -
Identifier Source: org_study_id
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