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RECRUITING NA

Cold and Compression Post TKA

NCT07023185 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to compare pain score (Patient-Reported Outcomes Measurement Information System: PROMIS NRS Pain Subscale) between the control and cold/compression groups pre-surgically, daily after surgery for 14 days, then weekly after surgery for 3 months, and at 6 months post-surgery.

Interventions

  • DEVICE Cold and Compression
  • OTHER SOC (Standard of care)

Study Locations (1)

Louisiana

  • Ochsner Medical Center - Kenner — New Orleans

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2025-12-15
Est. Completion 2028-06
Phase NA

Sponsor

Ochsner Health System

71 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07023185

The ClinicalTrials.gov registry entry for NCT07023185 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ochsner Health System, which has 71 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery appearing as the primary indexed condition, and to 2 interventions — of which Cold and Compression is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07023185 reports 1 study location spanning 1 distinct geographic area — top geographies include Louisiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07023185 about?

NCT07023185 is a clinical study titled "Cold and Compression Post TKA". The purpose of this study is to compare pain score (Patient-Reported Outcomes Measurement Information System: PROMIS NRS Pain Subscale) between the control and cold/compression groups pre-surgically, daily after surgery for 14 days, then weekly after surgery for 3 months, and at 6 months post-surger...

What is the current status of trial NCT07023185?

This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2025-12-15. Estimated completion is 2028-06.

What conditions does trial NCT07023185 study?

This clinical trial studies the following conditions: Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07023185?

The interventions under investigation include: Cold and Compression (DEVICE), SOC (Standard of care) (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07023185?

This trial is sponsored by Ochsner Health System, which has 71 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07023185 being conducted?

This trial has 1 study location across Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial