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NCT07151417 · ClinicalTrials.gov registry record · Phase 2

Use of Corticosteroid in Intraopertive Injections in Total Knee Replacement Surgery.

A Phase 2 study, sponsored by Walter Reed National Military Medical Center.

Not yet
Registry status
Phase 2
Development phase
240
Enrollment target

NCT07151417: Clinical Trial Phase 2 study, sponsored by Walter Reed National Military Medical Center.

NCT07151417 is a Phase 2 study that has not yet begun recruiting, run by Walter Reed National Military Medical Center. The registered enrollment target is 240 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07151417, a Phase 2 study, has not yet begun recruiting, sponsored by Walter Reed National Military Medical Center.

NOT YET RECRUITING
Registry status
Phase 2
Development phase
240 participants
Enrollment target

Study Summary

The goal of this clinical trial is to find out which type of steroid medicine, when added to a standard pain-control injection during total knee replacement surgery, works best at reducing pain, limiting opioid use, and improving recovery in adults undergoing surgery for severe knee arthritis or injury. The main questions it aims to answer are: Does adding a steroid to the injection improve pain control and reduce opioid use after surgery? Is the newer extended-release steroid (Zilretta) more effective and safer-especially for patients with diabetes-than the traditional steroid (methylprednisolone)? Researchers will compare: Standard pain-control injection alone Standard injection plus methylprednisolone Standard injection plus Zilretta to see which option provides better pain relief, less opioid use, and improved knee function. (Patients with diabetes or prediabetes will only be in the standard injection or Zilretta groups so researchers can study whether Zilretta is safer for blood sugar control.) Participants will: Be randomly assigned to one of the study groups during their total knee replacement surgery Receive the assigned pain-control injection around the knee joint Be followed after surgery to measure: Pain levels Opioid pain medication use Knee movement (range of motion) Whether another procedure (such as manipulation under anesthesia) is needed if the knee becomes too stiff Patient-reported outcome surveys about pain and function

Primary Outcome

The following outcomes after total knee arthroplasty will be compared to determine whether outcomes are significantly better for Zilretta (Group 3) and methylprednisolone (Group 2) as compared to standard PAI (Group 1) and Zilretta versus methylprednisolone: • Improvement in pain levels postoperatively based on measurement of pain intensity using a Visual Analogue Scale (VAS) at 24hrs, 72 hours, and 7 days (all phone call), and 28 days

Interventions

  • DRUG PAI
  • DRUG PAI + steroid
  • DRUG PAI + zilretta

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2025-09-01
Est. Completion 2026-08-31
Phase Phase 2

What is known before NCT07151417 opens enrollment

NCT07151417 is an interventional study that assigns participants to a tested intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (80% higher).

The record links to 0 conditions, and to 3 interventions - of which PAI is the first listed.

NCT07151417 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07151417 about?

NCT07151417 is a clinical study titled "Use of Corticosteroid in Intraopertive Injections in Total Knee Replacement Surgery.". The goal of this clinical trial is to find out which type of steroid medicine, when added to a standard pain-control injection during total knee replacement surgery, works best at reducing pain, limiting opioid use, and improving recovery in adults undergoing surgery for severe knee arthritis or inj...

What is the current status of trial NCT07151417?

This trial is currently not yet recruiting. It is a Phase 2 study. The enrollment target is 240 participants. The study started on 2025-09-01. Estimated completion is 2026-08-31.

What interventions are being tested in trial NCT07151417?

The interventions under investigation include: PAI (DRUG), PAI + steroid (DRUG), PAI + zilretta (DRUG).

Who is sponsoring clinical trial NCT07151417?

This trial is sponsored by Walter Reed National Military Medical Center, which has 48 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07151417's enrollment target sits among peer trials

240 239th of 2000 higher than 1,746 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT07151417, the US trial registry maintained by the National Library of Medicine. NCT07151417 (mid enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.