Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01833481 · ClinicalTrials.gov registry record

THA Kinematics and Sound for Subjects Implanted Using Various Surgical Approaches

A clinical trial, sponsored by The University of Tennessee, Knoxville.

Completed
Registry status
30
Enrollment target

NCT01833481: Completed study, sponsored by The University of Tennessee, Knoxville.

NCT01833481 is a clinical trial that has completed, run by The University of Tennessee, Knoxville. The registered enrollment target is 30 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01833481 has completed, sponsored by The University of Tennessee, Knoxville.

COMPLETED
Registry status
30 participants
Enrollment target

Study Summary

In a previous study conducted within the Center for Musculoskeletal Research (CMR) on Total Hip Arthroplasties (THA), it was determined that the investigators could simultaneously capture in vivo sound and motion of the femoral head within the acetabular cup during weight-bearing activities for subjects implanted with either a metal-on-polyethylene (MOP), metal-on-metal (MOM) or ceramic-on-ceramic (COC) THA. This was the first study to apply sound analysis as an impulse excitation technique for testing hip conditions and for measuring femoral head sliding in the acetabular component of human hip joints by acoustic means. Unfortunately, no studies have been conducted to compare the in vivo kinematics and sound for subjects implanted using various surgical approaches. It could be hypothesized that subjects having various surgical approaches could lead to an increase or reduction of in vivo hip separation. Therefore, the objective of this study is to analyze a total of 30 subjects implanted with either an anterior (10 patients), anterior-lateral (10 patients), or posterior-lateral (10 patients) surgical approach to determine if any of these surgical approaches leads to less or more in vivo hip separation. All subjects will be analyzed under in vivo weight-bearing conditions using video fluoroscopy to determine in vivo motion.

Primary Outcome

Determine amount of in vivo swing phase hip separation present within implanted hip during weight-bearing level walking while under fluoroscopic surveillance.

Interventions

  • RADIATION Fluoroscopy surveillance of patients while walking

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2013-06
Est. Completion 2014-09

What the finished NCT01833481 record still lists

NCT01833481 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 30 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which Fluoroscopy surveillance of patients while walking is the first listed.

NCT01833481 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01833481 about?

NCT01833481 is a clinical study titled "THA Kinematics and Sound for Subjects Implanted Using Various Surgical Approaches". In a previous study conducted within the Center for Musculoskeletal Research (CMR) on Total Hip Arthroplasties (THA), it was determined that the investigators could simultaneously capture in vivo sound and motion of the femoral head within the acetabular cup during weight-bearing activities for subj...

What is the current status of trial NCT01833481?

This trial is currently completed. The enrollment target is 30 participants. The study started on 2013-06. Estimated completion is 2014-09.

What interventions are being tested in trial NCT01833481?

The interventions under investigation include: Fluoroscopy surveillance of patients while walking (RADIATION).

Who is sponsoring clinical trial NCT01833481?

This trial is sponsored by The University of Tennessee, Knoxville, which has 81 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01833481, the US trial registry maintained by the National Library of Medicine. NCT01833481 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.