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NCT01420237 · ClinicalTrials.gov registry record · NA

Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study

A NA study, sponsored by Stryker Orthopaedics.

Terminated
Registry status
NA
Development phase
367
Enrollment target

NCT01420237: Clinical Trial NA study, sponsored by Stryker Orthopaedics.

NCT01420237 is a NA study that was terminated before completion, run by Stryker Orthopaedics. The registered enrollment target is 367 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (74% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01420237, a NA study, was terminated before completion, sponsored by Stryker Orthopaedics.

TERMINATED
Registry status
NA
Development phase
367 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the success rate of cementless primary hip replacement with the Restoration® ADM X3® Acetabular System as compared to other primary hip systems in the literature, through absence of femoral head dislocation at 10 years postoperative.

Primary Outcome

Defined as absence of postoperative femoral head dislocation.

Interventions

  • DEVICE Restoration ADM X3 Device

Trial Details

FieldValue
Enrollment Target 367 participants
Start Date 2011-06
Est. Completion 2023-11-09
Phase NA
Stryker Orthopaedics

27 total trials

Why NCT01420237 stopped before completion

NCT01420237 is an interventional study that assigns participants to a tested intervention. The registered 367 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 (74% lower).

The record links to 0 conditions, and to 1 intervention - of which Restoration ADM X3 Device is the first listed.

NCT01420237 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01420237 about?

NCT01420237 is a clinical study titled "Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Study". The purpose of this study is to evaluate the success rate of cementless primary hip replacement with the Restoration® ADM X3® Acetabular System as compared to other primary hip systems in the literature, through absence of femoral head dislocation at 10 years postoperative.

What is the current status of trial NCT01420237?

This trial is currently terminated. It is a NA study. The enrollment target is 367 participants. The study started on 2011-06. Estimated completion is 2023-11-09.

What interventions are being tested in trial NCT01420237?

The interventions under investigation include: Restoration ADM X3 Device (DEVICE).

Who is sponsoring clinical trial NCT01420237?

This trial is sponsored by Stryker Orthopaedics, which has 27 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01420237's enrollment target sits among peer trials

367 284th of 2000 higher than 1,717 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 NCT01420237, the US trial registry maintained by the National Library of Medicine. NCT01420237 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.