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NCT04533880 · ClinicalTrials.gov registry record · NA

The Effect of Bone-void Filler on Anterior Knee Pain Following ACL Reconstruction

A NA study, sponsored by NYU Langone Health.

Completed
Registry status
NA
Development phase
150
Enrollment target

NCT04533880: Completed NA study, sponsored by NYU Langone Health.

NCT04533880 is a NA study that has completed, run by NYU Langone Health. The registered enrollment target is 150 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04533880, a NA study, has completed, sponsored by NYU Langone Health.

COMPLETED
Registry status
NA
Development phase
150 participants
Enrollment target

Study Summary

One of the common complaints after ACLR with BPTB autograft anterior knee pain. It is thought that this may be due to harvesting the patellar tendon for graft use. Specifically, this may be due to the bone defect that is left after graft harvesting. There is currently no consensus on a gold standard for treating the bone defect with surgeons using multiple commercially available bone void fillers as well as autologous bone graft in standard practice. The purpose of the proposed study is to evaluate the effect bone-void filler on anterior knee pain following ACL reconstruction BPTB autograft.

Primary Outcome

The KOOS survery comprises 42 questions; questions are divided into 5 sub-categories: symptoms (7 questions), pain (9 questions), function/daily living (17 questions), function/sports and recreational activities (5 questions), quality of life (4 questions). Each item is rated on a Likert scale from 0 to 4. The score is calculated by summing the responses. The total range for each sub-category is 0-100, making the total range for the whole survey 0-500. The higher the score, the worse the symptom

Interventions

  • DEVICE DBM
  • DEVICE Calcium phosphate cement
  • OTHER Autologous bone graft

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2020-08-31
Est. Completion 2023-07-07
Phase NA
NYU Langone Health

1,164 total trials

What the finished NCT04533880 record still lists

NCT04533880 is an interventional study that assigns participants to a tested intervention. The registered 150 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 (89% lower).

The record links to 0 conditions, and to 3 interventions - of which DBM is the first listed.

NCT04533880 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04533880 about?

NCT04533880 is a clinical study titled "The Effect of Bone-void Filler on Anterior Knee Pain Following ACL Reconstruction". One of the common complaints after ACLR with BPTB autograft anterior knee pain. It is thought that this may be due to harvesting the patellar tendon for graft use. Specifically, this may be due to the bone defect that is left after graft harvesting. There is currently no consensus on a gold standard...

What is the current status of trial NCT04533880?

This trial is currently completed. It is a NA study. The enrollment target is 150 participants. The study started on 2020-08-31. Estimated completion is 2023-07-07.

What interventions are being tested in trial NCT04533880?

The interventions under investigation include: DBM (DEVICE), Calcium phosphate cement (DEVICE), Autologous bone graft (OTHER).

Who is sponsoring clinical trial NCT04533880?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04533880's enrollment target sits among peer trials

150 661st of 2000 higher than 1,299 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 NCT04533880, the US trial registry maintained by the National Library of Medicine. NCT04533880 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.