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Multicenter Outcome Registry of AnaLgesic Effect of SCS(MORALES) Registry Protocol

NCT04548375 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2024-08-20

No results posted yet for this study

Summary

The objective is to provide information to help the physician community decide the most effective type of device/therapy that would work for their patients, based off of the etiology of pain, the location of the pain for sustained pain relief.

Conditions

  • SCS

Interventions

DEVICE

SCS

Conventional SCS implants approved through all payors(government and private) for FDA approved indications

Sponsors & Collaborators

  • Cardio Surgical Partners

    lead NETWORK

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-11-01
Primary Completion
2026-11-01
Completion
2026-11-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04548375 on ClinicalTrials.gov