New Orleans, LANCT07023185Now EnrollingIRB Ready

Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery Clinical Trial in New Orleans, LA

Access cutting-edge primary osteoarthritis patients scheduled for total knee replacement surgery treatment through this clinical trial at a research site in New Orleans. Study-provided care at no cost to qualified participants.

Sponsored by Ochsner Health System

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Expert Care in New Orleans

Access primary osteoarthritis patients scheduled for total knee replacement surgery specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related primary osteoarthritis patients scheduled for total knee replacement surgery treatment provided free

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Check if you qualify for this primary osteoarthritis patients scheduled for total knee replacement surgery clinical trial in New Orleans, LA

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Why Participate?

  • No-Cost Study Care

  • Local to New Orleans

    Convenient for LA residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit New Orleans site if eligible
  4. 4Begin participation

About This Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery Study in New Orleans

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.

Sponsor: Ochsner Health System

Who Can Participate

Inclusion Criteria

Aged 50 yr or older
Patient of Dr. Howard Hirsch or Dr. Vinod Dasa scheduled for total knee arthroplasty (knee replacement) at Ochsner Kenner
Will receive outpatient physical therapy at OTW Driftwood for the entire post-op rehabilitation period
English speaking
Diagnosis of primary osteoarthritis

Exclusion Criteria

Chronic opioid use
Opioid use within the last 3 months
PCS score ≥ 30
Diagnosis of inflammatory disease process (i.e., gout, rheumatoid arthritis, systematic lupus erythematosus...)
Discharge to skilled nursing
Cold intolerance related to diseases, like Raynaud's
Significant vascular impairment in the affected region
Current clinical signs of inflammatory phlebitis, venous ulcers, or cellulitis
Significant risk factors or current clinical signs of embolism (e.g., pulmonary embolus, pulmonary edema, cerebral infarction, atrial fibrillation, endocarditis, myocardial infarction, or atheromatous embolic plaque)
A condition in which increased venous or lymphatic return is not desired in the affected extremity (e.g., lymphedema after breast cancer or other local carcinoma and/or carcinoma metastasis in the affected extremity).
Uncontrolled hypertension (physician discretion), cardiac failure, extreme low blood pressure, or decompensated cardiac insufficiency.
Localized unstable skin condition (e.g., dermatitis, vein ligation, gangrene, or recent skin graft) in the affected region.
Had recent toe surgery in the affected region
Current clinical signs in the affected region of significant peripheral edema (e.g., deep vein thrombosis, chronic venous insufficiency, acute compartment syndrome, systemic venous hypertension, congestive heart failure, cirrhosis/liver failure, renal failure).
An acute, unstable (untreated) fracture in the affected region.
Any active local or systemic infection.
Obtunded or with diabetes mellitus, multiple sclerosis, poor circulation, spinal cord injuries, and rheumatoid arthritis
Areas of skin breakdown or damage (damaged or at-risk skin) producing uneven heat conduction across the skin (e.g., open wound, scar tissue, burn or skin graft). Any open wound must be dressed prior to use of the Polar Care Wave System.
Presumptive evidence of congestive heart failure
Pre-existing DVT condition
Deep acute venal thrombosis (Phlebothrombosis)
Episodes of pulmonary embolism
Pulmonary edema
Acute inflammation of the veins (Thrombophlebitis)
Decompensated cardiac insufficiency
Arterial dysregulation
Carcinoma and carcinoma metastasis in the affected extremity
Decompensated hypertonia
Acute inflammatory skin diseases or infection
Venous or arterial occlusive disease
Medical situations where increased venous or lymphatic return is undesirable
Poor peripheral circulation
Severe arteriosclerosis, or active infection
Known hematological dyscrasias that predispose to thrombosis (e.g., paroxysmal cold hemoglobinuria, cryoglobulinemia, sicklecell disease, serum cold agglutinins).
Tissues inflamed as a result of recent injury or exacerbation of chronic inflammatory condition.
Compromised local circulation or neurologic impairment (including paralysis or localized compromise due to multiple surgical procedures or diabetes) in the affected region.
Cognition or communication impairments that prevent them from giving accurate and timely feedback.
Cold allergy
Cold agglutinin disorders like paroxysmal cold hemoglobinuria
Buerger's disease
Cryoglobulinemia
Sickle cell anemia
Uncontrolled diabetes (physician discretion)
Hypersensitivity to cold
History of cold injury
Severe cardiovascular disease, anesthetic skin, hypercoagulation disorders, poor circulation, extremities sensitive to pain, extremely low blood pressure that are incapacitated, decreased skin sensitivity, vein ligation or recent skin grafts, or pheochromocytoma.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in New Orleans?

Yes, this clinical trial (NCT07023185) has an active research site in New Orleans, LA that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Primary Osteoarthritis Patients Scheduled for Total Knee Replacement Surgery Treatment Options in New Orleans, LA

If you're searching for primary osteoarthritis patients scheduled for total knee replacement surgery treatment options in New Orleans, LA, this clinical trial (NCT07023185) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our New Orleans research site is actively enrolling participants for this clinical trial. You'll receive care from experienced primary osteoarthritis patients scheduled for total knee replacement surgery specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all primary osteoarthritis patients scheduled for total knee replacement surgery clinical trials near you to find additional studies recruiting in your area.

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