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
PHASE4
197 participants
INTERVENTIONAL
2022-09-01
2022-11-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Patients using intrauterine lidocaine for analgesia
Analgesic
comparing the effectiveness of analgesics in endometrial biopsy
Patients using oral dexketoprofen for analgesia
Analgesic
comparing the effectiveness of analgesics in endometrial biopsy
Patients using cervical lidocaine spray for analgesia
Analgesic
comparing the effectiveness of analgesics in endometrial biopsy
Patients using paracervical block with prilocaine for analgesia
Analgesic
comparing the effectiveness of analgesics in endometrial biopsy
Interventions
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Analgesic
comparing the effectiveness of analgesics in endometrial biopsy
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* women with a history of severe uncontrolled cardiovascular disease, diabetes mellitus, pregnancy, vaginal, cervical, or pelvic infection, cervical cancer, or severe cervical stenosis
18 Years
75 Years
FEMALE
No
Sponsors
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Gaziosmanpasa Research and Education Hospital
OTHER_GOV
Responsible Party
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Locations
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Gaziosmanpaşa Training and Research Hospital
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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GaziosmanpasaTREHes
Identifier Type: -
Identifier Source: org_study_id
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