Gynecological Presentations Following Supracervical Hysterectomy
NCT ID: NCT03606772
Last Updated: 2019-06-12
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
130 participants
OBSERVATIONAL
2018-08-01
2019-03-31
Brief Summary
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Detailed Description
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* Patients: 130 patients with hysterectomy recruited at Tanta University Hospital, gynecology clinics in central hospitals in Gharbia governorate will be recruited according inclusion and exclusion criteria. Inclusion criteria include all symptomatizing patients following supracervical hysterectomy, of any age, of any complaints. The
* Methods: All patients' demographic data, history, indication of hysterectomy, duration since operation, postoperative complications and their main complaint.
Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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supracervical hysterectomy
Patients operated abdominal by removal of uterus, with removal of tubes and ovaries and retaining of cervix
Questionanniare
Filling printed questionnaire + Pelvic examination
Interventions
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Questionanniare
Filling printed questionnaire + Pelvic examination
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
35 Years
60 Years
FEMALE
No
Sponsors
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Tanta University
OTHER
Responsible Party
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Ayman S Dawood, MD
Lecturer
Principal Investigators
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Ayman Dawood
Role: PRINCIPAL_INVESTIGATOR
Lecturer at Tanta University
Locations
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Ayman Shehata Dawood
Tanta, Algharbia, Egypt
Countries
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Other Identifiers
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GPHysterectomy
Identifier Type: -
Identifier Source: org_study_id
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