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NCT07197775Enrolling by invitation

Post-market SUrveiLlance RegiStry for the Endogenex System (Endogenex PULSE Registry)

Endogenex PULSE Registry

Source: ClinicalTrials.gov · Last updated 1 Jul 2026

Brief summary (registry, in English)

This registry is designed to collect long-term data and support ongoing post-market surveillance of real-world data for the Endogenex System.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
500 (estimated)
First submitted
26 Sept 2025
Start date
11 Mar 2026
Primary completion date
May 2032
Lead sponsor
Endogenex, Inc.
NCT number
NCT07197775

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 11 Mar 2026 to the primary completion date, May 2032
  • 4 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Unwilling or unable to attend study visits
  • Unwilling or unable to provide medical records to study sites

Who the study is looking for

  • Type 2 diabetes
  • Have been treated with the Endogenex System
  • Consented to participate in the Endogenex PULSE Registry

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
St Vincent's Hospital Melbourne
Coordinator of this site? Confirm its status
FitzroyAustraliaUnknown status
Care Access
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Care Access
Coordinator of this site? Confirm its status
QuincyUnited StatesUnknown status
Care Access
Coordinator of this site? Confirm its status
RaleighUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.