Expired Study
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Maywood, Illinois 60153


Purpose:

The purpose of this study is to evaluate if lidocaine-prilocaine (EMLA 5%) cream can reduce pain and discomfort at the time of vaginal pessary removal and insertion. Half of the participants will receive lidocaine-prilocaine (EMLA 5%) cream and the other half will receive a placebo cream.


Study summary:

Lidocaine-prilocaine (EMLA 5%) cream has been shown to be effective in reducing pain during minor gynecologic procedures. The primary objective of this trial is to determine if the use of 5% EMLA cream at the time of pessary removal and insertion reduces pain when compared to the use of placebo cream. Participants will be randomized to receive either 10 grams of 5% EMLA cream (4 mL) or 4 mL of placebo cream (aqueous cream BP). Cream will be applied in office at the time of pessary removal and insertion.


Criteria:

Inclusion Criteria: - Women in the Loyola Urogynecology clinic who use a pessary for management of pelvic organ prolapse (POP) or urinary incontinence (UI) - Read and speak the English language Exclusion Criteria: - Non-English speaking - Allergy or contraindication to topical anesthetic - Participation/randomization in the study at a previous visit - Currently pregnant or lactating or planning a pregnancy within the next 6 months


NCT ID:

NCT02380742


Primary Contact:

Principal Investigator
Cynthia Brincat, MD
Loyola University


Backup Contact:

N/A


Location Contact:

Maywood, Illinois 60153
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 23, 2017

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