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NCT03341442 · ClinicalTrials.gov registry record · NA

A Study of Posterior Hip Precautions After Total Hip Arthroplasty

A NA study, sponsored by West Virginia University.

Completed
Registry status
NA
Development phase
321
Enrollment target

NCT03341442: Completed NA study, sponsored by West Virginia University.

NCT03341442 is a NA study that has completed, run by West Virginia University. The registered enrollment target is 321 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03341442, a NA study, has completed, sponsored by West Virginia University.

COMPLETED
Registry status
NA
Development phase
321 participants
Enrollment target

Study Summary

The purpose of this study is to perform a randomized controlled study to compare patients undergoing THA via a posterolateral approach to receive either standard of care post-surgery hip restrictions or to receive no restrictions. The investigators goal is to first complete a pilot study in which the investigators assess the short term dislocation rates 3-6 months and then continue to recruit into this study and follow these patients for a year to determine the 1 year risk for dislocation. The investigators also will compare the HOOS Jr. and VAS scores and time until free from walking aid. The research question is: Will the elimination of post operative posterior hip precautions increase the dislocation rate? The hypothesis is that the elimination of post operative hip precautions will not increase the dislocation rate.

Primary Outcome

Occurrence of dislocations will be compared between groups.

Interventions

  • PROCEDURE No hip precautions

Trial Details

FieldValue
Enrollment Target 321 participants
Start Date 2016-04
Est. Completion 2020-06
Phase NA
West Virginia University

122 total trials

What the finished NCT03341442 record still lists

NCT03341442 is an interventional study that assigns participants to a tested intervention. The registered 321 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 (77% lower).

The record links to 0 conditions, and to 1 intervention - of which No hip precautions is the first listed.

NCT03341442 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03341442 about?

NCT03341442 is a clinical study titled "A Study of Posterior Hip Precautions After Total Hip Arthroplasty". The purpose of this study is to perform a randomized controlled study to compare patients undergoing THA via a posterolateral approach to receive either standard of care post-surgery hip restrictions or to receive no restrictions. The investigators goal is to first complete a pilot study in which th...

What is the current status of trial NCT03341442?

This trial is currently completed. It is a NA study. The enrollment target is 321 participants. The study started on 2016-04. Estimated completion is 2020-06.

What interventions are being tested in trial NCT03341442?

The interventions under investigation include: No hip precautions (PROCEDURE).

Who is sponsoring clinical trial NCT03341442?

This trial is sponsored by West Virginia University, which has 122 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03341442's enrollment target sits among peer trials

321 315th of 2000 higher than 1,686 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 NCT03341442, the US trial registry maintained by the National Library of Medicine. NCT03341442 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.