Active — Not RecruitingNot Applicable

VIA Disc NP Registry 3.0

United States500 participantsStarted 2024-02-27

Plain-language summary

Registry is to observe and trend patterns of care and outcomes for patients treated with VIA Disc NP.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Willing to sign the informed consent and deemed capable of complying with the requirements of the study protocol
. 18 years of age or older
. Literate, able to speak and read English, and able to complete questionnaires independently
. Subject received a VIA Disc NP injection with 1 or more levels within 90 days of the baseline visit.

Exclusion criteria

. Participant did not receive VIA Disc NP injection
. Participant is pregnant (self-reported, no special study pregnancy testing needed).
. Any contraindications as noted in the VIA Disc NP Instructions for Use
. Previous treatment with VIA Disc NP

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Numeric Pain Rating Scale (NPRS)

Timeframe: 1, 3, 6, & 12 months

Oswestry Disability Index (ODI)

Timeframe: 1, 3, 6, & 12 months

Patient Satisfaction

Timeframe: 1, 3, 6, & 12 months

Frequency of Pain Medication Use

Timeframe: 1, 3, 6, & 12 months

Trial details

NCT IDNCT06345690

SponsorVIVEX Biologics, Inc.

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2027-01-01

View on ClinicalTrials.gov More Discogenic Pain trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Willing to sign the informed consent and deemed capable of complying with the requirements of the study protocol
. 18 years of age or older
. Literate, able to speak and read English, and able to complete questionnaires independently
. Subject received a VIA Disc NP injection with 1 or more levels within 90 days of the baseline visit.

Exclusion criteria

. Participant did not receive VIA Disc NP injection
. Participant is pregnant (self-reported, no special study pregnancy testing needed).
. Any contraindications as noted in the VIA Disc NP Instructions for Use
. Previous treatment with VIA Disc NP