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ENROLLING BY INVITATION
NCT06903767
NA

Automated V Manual Impactor Study

Sponsor: Rothman Institute Orthopaedics

View on ClinicalTrials.gov

Summary

This study investigates the use of an automated impactor device in total hip arthroplasty versus manual malleting method and the physiological strain on the surgeon. This study will be a randomized, prospective, multicenter study involving fellowship-trained arthroplasty surgeons. Each participating surgeon will contribute data from 50 primary, elective THA cases, using the HAMMR powered impactor in 25 cases and manual impaction in 25 cases.

Official title: Do Quantifiable Differences in Physiologic Stress Exist in Surgeons When Comparing the Use of a Powered Femoral Impactor Versus Manual Impaction in Total Hip Arthroplasty?

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

200

Start Date

2025-03-25

Completion Date

2026-03-31

Last Updated

2025-04-01

Healthy Volunteers

Yes

Interventions

DEVICE

Automated Impaction (HAMMR)

For cases that are randomized to the automated impaction HAMMR group, the surgeon will utilize an automated impactor device for impaction of the implant during total hip arthroplasty.

DEVICE

Manual Malleting

For cases that are randomized to the manual malleting group, the surgeon will utilize a mallet for impaction of the implant during total hip arthroplasty.

Locations (1)

Rothman Orthopaedic Institute

Philadelphia, Pennsylvania, United States