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IT Matters: The Erectile Restoration Registry

← catalyst calendar

NCT04200937 · readout ≤ 1,625 d

Sponsored by Boston Scientific Corporation (industry) · BSX — their whole pipeline →.

Phase
Status
Enrolling by invitation
Study type
Observational
Enrollment
450estimated
Sites
25
Countries
China, Saudi Arabia, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-08-05actualWhen the study began enrolling
Primary completionJan 2031estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2031estimatedThe whole study's end, after follow-up
First posted2019-12-16actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-12actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Erectile Dysfunction

Interventions

  • Device: Tactra Malleable
  • Device: Spectra™ Concealable Penile Prothesis
  • Device: AMS Ambicor™ Inflatable Penile Prosthesis
  • Device: AMS 700™ Inflatable Penile Prosthesis w/Momentary Squeeze (MS) Pump
  • Device: AMS 700™ Inflatable Penile Prosthesis w/Tenacio™ Pump

Primary outcome

what the primary-completion date above is the date OF
Change from baseline to six months in the Erectile Function domain ofthe International Index of Erectile Function (IIEF-EF) questionnaire for Tactra
measured Baseline to 6 months

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