Ignite Creation Date:
2024-05-05 @ 4:45 PM
Last Modification Date:
2024-10-26 @ 9:23 AM
Study NCT ID:
NCT00308841
Status:
COMPLETED
Last Update Posted:
2008-10-20
First Post:
2006-03-29
Brief Title:
Anesthetic Efficacy of Intrauterine Lidocaine for Removal of a Lost Intrauterine Device
Sponsor:
Suleyman Demirel University
Organization:
Suleyman Demirel University
Study Overview
Official Title:
None
Status:
COMPLETED
Status Verified Date:
2005-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
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 Friedmans test with Bonferroni correction Students t test and 2
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 Friedmans test with Bonferroni correction Students t test and 2
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None