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NCT04062630 · ClinicalTrials.gov registry record · NA

SI Joint Stabilization in Long Fusion to the Pelvis

A NA study, sponsored by SI-BONE.

Completed
Registry status
NA
Development phase
213
Enrollment target

NCT04062630: Completed NA study, sponsored by SI-BONE.

NCT04062630 is a NA study that has completed, run by SI-BONE. The registered enrollment target is 213 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT04062630, a NA study, has completed, sponsored by SI-BONE.

COMPLETED
Registry status
NA
Development phase
213 participants
Enrollment target

Study Summary

The purpose of this study is to compare outcomes of subjects undergoing multilevel lumbar fusion (MLF) surgery with and without the iFuse 3-D implants in the "bedrock" trajectory.

Primary Outcome

Proportion of subjects with any of following: S2AI screw breakage, loosening or pullout OR rod breakage distal to S1 on 2-year CT scan as interpreted by an independent bone radiologist

Interventions

  • DEVICE iFuse 3-D in Bedrock Configuration
  • PROCEDURE Multilevel Lumbar Fusion surgery

Trial Details

FieldValue
Enrollment Target 213 participants
Start Date 2020-05-20
Est. Completion 2025-01-15
Phase NA
SI-BONE

10 total trials

What the finished NCT04062630 record still lists

NCT04062630 is an interventional study that assigns participants to a tested intervention. The registered 213 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 2 interventions - of which iFuse 3-D in Bedrock Configuration is the first listed.

NCT04062630 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04062630 about?

NCT04062630 is a clinical study titled "SI Joint Stabilization in Long Fusion to the Pelvis". The purpose of this study is to compare outcomes of subjects undergoing multilevel lumbar fusion (MLF) surgery with and without the iFuse 3-D implants in the "bedrock" trajectory.

What is the current status of trial NCT04062630?

This trial is currently completed. It is a NA study. The enrollment target is 213 participants. The study started on 2020-05-20. Estimated completion is 2025-01-15.

What interventions are being tested in trial NCT04062630?

The interventions under investigation include: iFuse 3-D in Bedrock Configuration (DEVICE), Multilevel Lumbar Fusion surgery (PROCEDURE).

Who is sponsoring clinical trial NCT04062630?

This trial is sponsored by SI-BONE, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04062630's enrollment target sits among peer trials

213 488th of 2000 higher than 1,512 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT04062630, the US trial registry maintained by the National Library of Medicine. NCT04062630 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.