Anesthetic Efficacy of Intrauterine Lidocaine for Removal of a "Lost" Intrauterine Device
NCT ID: NCT00308841
Last Updated: 2008-10-20
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
PHASE1
INTERVENTIONAL
Brief Summary
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Methods: This double-blinded, randomized, placebo-controlled trial included 68 women who underwent removal procedure for a "lost" IUD. Thirty-four women were allocated to the lidocaine group and 34 to the saline group. The main outcome measure was the intensity of pain during, immediately after, and 20 minutes after the procedure, assessed by a visual analog scale. Statistical analysis was performed using Friedman's test with Bonferroni correction, Student's t test, and 2.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
DOUBLE
Interventions
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Lidocaine (drug)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
FEMALE
No
Sponsors
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Suleyman Demirel University
OTHER
Principal Investigators
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Mehmet Güney, M.D
Role: PRINCIPAL_INVESTIGATOR
SDU
Locations
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Süleyman Demirel University, School of Medicine
Isparta, , Turkey (Türkiye)
Countries
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References
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Guney M, Oral B, Mungan T. Efficacy of intrauterine lidocaine for removal of a "lost" intrauterine device: a randomized, controlled trial. Obstet Gynecol. 2006 Jul;108(1):119-23. doi: 10.1097/01.AOG.0000223201.42144.80.
Other Identifiers
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B.30.2.SDÜ.0.01.00.01.301.01
Identifier Type: -
Identifier Source: org_study_id
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