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NCT03770169

Validation of Patient Reported Outcome Measures for Use in Vulvodynia

Completed Last updated 28 October 2019
What this trial tests

trial in Vulvodynia in 20 participants. Completed in 19 September 2019.

Timeline
18 February 2019
Primary endpoint
19 September 2019
19 September 2019

Quick facts

Lead sponsorIpsen
StatusCompleted
Study typeOBSERVATIONAL
Enrollment20
Start date18 February 2019
Primary completion19 September 2019
Estimated completion19 September 2019
Sites4 locations across United States

Conditions studied

Sponsor

Ipsen — full company profile →

Who can join

Adults 18 to 45, female only, with Vulvodynia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The overall aim of this project is to demonstrate content validity and usability of the modified Vulvar Pain Assessment Questionnaire (mVPAQ), the modified Female Sexual Function Index (mFSFI), and pain on intercourse Numeric Rating Scale (NRS) for adult patients with Vulvodynia

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Vulvodynia

Currently open trials in the same condition.

Other Ipsen trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03770169.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing