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THA With and Without Computer Navigation

S

Southeast Orthopedic Specialists

Status

Completed

Conditions

Avascular Necrosis of Hip
Hip Osteoarthritis

Treatments

Procedure: Intraoperative Fluoroscopic Computer Navigation

Study type

Observational

Funder types

NETWORK

Identifiers

NCT05871827
DPS-JMP-2019-078

Details and patient eligibility

About

The goal of this observational study is to compare postoperative results between patients who had total hip arthroplasty (THA) with and without the use of a computer navigation program. The main questions this study aims to answer are:

  • Can using computer navigation produce better THA implant placement?
  • Can using computer navigation make surgery more efficient?

Participant data collected include their postoperative x-rays and total operative time.

Full description

The goal of this retrospective study is to compare implant placement and operative time of patients who underwent direct anterior total hip arthroplasty with and without the use of a computer navigation program. X-rays are used to measure acetabular cup orientation, leg length discrepancy, and total operative time.

Enrollment

234 patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who underwent Direct Anterior (DA) THA with the principal investigator between August 2018 and February 2020 and received ACTIS stem and PINNACLE cup with or without computer navigation

Exclusion criteria

  • Patients who underwent subsequent revision THA, conversion arthroplasty, hybrid procedures, experienced native or postoperative dislocations, and missing or inadequate radiographs at time of data collection.

Trial design

234 participants in 2 patient groups

Traditional Overlay
Description:
Subjects who underwent THA without use of computer navigation
Computer Navigation
Description:
Subjects who underwent THA with use of computer navigation
Treatment:
Procedure: Intraoperative Fluoroscopic Computer Navigation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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