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NCT01996371 · ClinicalTrials.gov registry record · NA
Radiographic and Clinical Outcomes Following Unilateral or Bilateral Posterior Fixation in MI-TLIF
A NA study, sponsored by H Francis Farhadi, MD, PhD.
- Terminated
- Registry status
- NA
- Development phase
- 15
- Enrollment target
NCT01996371: Clinical Trial NA study, sponsored by H Francis Farhadi, MD, PhD.
NCT01996371 is a NA study that was terminated before completion, run by H Francis Farhadi, MD, PhD. The registered enrollment target is 15 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01996371, a NA study, was terminated before completion, sponsored by H Francis Farhadi, MD, PhD.
- TERMINATED
- Registry status
- NA
- Development phase
- 15 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the healing of the patients spine at 24-months following surgery and screw placement among 3 groups. The doctor will also compare clinical outcomes and the immediate and delayed medical and surgical complications among the 3 study groups. The goal of this study is to determine if treating patients with one of the 3 groups is better than the others.
Primary Outcome
Primary Outcome: To compare bony fusion rates at two years among the three study arms, using the Brantigan, Steffee and Fraser scale. Post-operative CT scans will be evaluated at 24 months for evidence of new solid osseous trabeculations bridging across the interspace.
Interventions
- DEVICE Pedicle Screw
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2014-01 |
| Est. Completion | 2020-05 |
| Phase | NA |
Why NCT01996371 stopped before completion
NCT01996371 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Pedicle Screw is the first listed.
NCT01996371 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01996371 about?
NCT01996371 is a clinical study titled "Radiographic and Clinical Outcomes Following Unilateral or Bilateral Posterior Fixation in MI-TLIF". The purpose of this study is to compare the healing of the patients spine at 24-months following surgery and screw placement among 3 groups. The doctor will also compare clinical outcomes and the immediate and delayed medical and surgical complications among the 3 study groups. The goal of this stud...
What is the current status of trial NCT01996371?
This trial is currently terminated. It is a NA study. The enrollment target is 15 participants. The study started on 2014-01. Estimated completion is 2020-05.
What interventions are being tested in trial NCT01996371?
The interventions under investigation include: Pedicle Screw (DEVICE).
Who is sponsoring clinical trial NCT01996371?
This trial is sponsored by H Francis Farhadi, MD, PhD, which has 2 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01996371's enrollment target sits among peer trials
15 1881st of 2000 higher than 92 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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