IT Matters: The Erectile Restoration Registry
← catalyst calendarNCT04200937 · 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| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2021-08-05 | actual | When the study began enrolling |
| Primary completion | Jan 2031 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | Dec 2031 | estimated | The whole study's end, after follow-up |
| First posted | 2019-12-16 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-08-12 | actual | The 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 OFChange 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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