Innovative Spinopelvic Solutions with Real-World Evidence (INSPIRE)

SI-Bone

Status: Invitation-only

Conditions: Sacroiliac Joint Pain; Sacroiliac Joint Dysfunction

Treatments: Other: Health questionnaires

Study type: Observational

Funder types: Industry

Identifiers

NCT06706908

302022

Details and patient eligibility

About

INSPIRE is a prospective decentralized study evaluating post-operative health outcomes in patients who undergo a procedure using implants manufactured by SI-BONE.

Enrollment: 1,000 estimated patients

Sex: All

Ages: 21+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Age > 21 at time of screening.
2. Patient will undergo a procedure utilizing an iFuse Implant family product.
3. Patient is comfortable communicating in written and spoken English.
4. Patient is willing and able to complete study questionnaires online, using either a smartphone, tablet, or computer.
5. Patient is willing and able to provide informed consent to participate

Exclusion criteria

1. Patient has fibromyalgia.
2. Patient has a pain pump.
3. Patient is currently receiving or seeking worker's compensation, disability remuneration, and/or involved in injury litigation