Anesthetic Efficacy of Intrauterine Lidocaine for Removal of a "Lost" Intrauterine Device

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Study Classification

INTERVENTIONAL

Brief Summary

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Objective: To evaluate the efficacy of intrauterine lidocaine instillation in reducing patient discomfort during the removal of a "lost" intrauterine device (IUD).

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.

Detailed Description

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Conditions

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"Lost" IUD

Keywords

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Objective: To evaluate the efficacy of intrauterine lidocaine instillation in reducing patient discomfort during the removal of a "lost" IUD

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Lidocaine (drug)

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

patients undergoing a minor gynecologic procedure for removal of a "lost" IUD.

Exclusion Criteria

women with a history of cervical stenosis, known allergy to lidocaine, pregnancy, acute cervicitis

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

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)

Site Status

Countries

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Turkey (Türkiye)

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.

Reference Type RESULT

PMID: 16816065 (View on PubMed)

Other Identifiers

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B.30.2.SDÜ.0.01.00.01.301.01

Identifier Type: -

Identifier Source: org_study_id