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Group 1: immediate weight bearing for Postoperative Pain

N/A
Waitlist Available
Research Sponsored by Rothman Institute Orthopaedics
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
femoral revision patients with the use of a modern titanium, fluted, tapered stem.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1 year
Awards & highlights

Study Summary

This study is evaluating whether weight bearing after a revision surgery is better for patients.

Eligible Conditions
  • Postoperative Pain
  • Hip Replacement

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Implant survival
Postoperative Complications
Return to function

Trial Design

2Treatment groups
Experimental Treatment
Group I: Group 2: 6 week toe touch weight bearingExperimental Treatment1 Intervention
Group II: Group 1: immediate weight bearingExperimental Treatment1 Intervention

Find a Location

Who is running the clinical trial?

Rothman Institute OrthopaedicsLead Sponsor
121 Previous Clinical Trials
21,409 Total Patients Enrolled
2 Trials studying Postoperative Pain
354 Patients Enrolled for Postoperative Pain

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Recent research and studies
clinicaltrials.govStudy
Trial of Weight Bearing Status Following Femoral Revision With Tapered, Fluted, Titanium Stems
2020. "Trial of Weight Bearing Status Following Femoral Revision With Tapered, Fluted, Titanium Stems". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04592939.
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~38 spots leftby Apr 2025
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