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Lidocaine for Sexual Dysfunction
Phase 4
Waitlist Available
Led By David Bender, MD
Research Sponsored by David Bender
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Female
Age 18-99
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 9 months
Awards & highlights
Study Summary
This study is evaluating whether a cream applied to the vagina may help reduce pain during sexual intercourse for women who have had surgery for gynecologic cancer.
Eligible Conditions
- Gynecologic Cancers
- Sexual Dysfunction
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 9 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~9 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Changes in Pain
Changes in Sexual Function
Secondary outcome measures
Adverse Childhood Events
Anxiety
Depressive Symptoms
+5 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: LidocaineActive Control1 Intervention
Patients being treated for gynecologic cancer assigned aqueous lidocaine solution as intervention to use during sexual encounters.
Group II: PlaceboPlacebo Group1 Intervention
Patients being treated for gynecologic cancer assigned placebo solution as intervention to use during sexual encounters.
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Who is running the clinical trial?
David BenderLead Sponsor
David Bender, MDPrincipal Investigator - University of Iowa
University of Iowa Chemical Dependency Center, University of Iowa Hospitals & Clinics
Finch U Of Hs/Chicago Medical Sch (Medical School)
University Hlth Ctr Of Pittsburgh (Residency)
Frequently Asked Questions
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