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Nanoscopic Meniscectomy vs Standard Meniscectomy for Meniscus Tears
N/A
Recruiting
Research Sponsored by Marshall University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 hours
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new, smaller surgical tool called a Nanoscope for knee surgery on patients with meniscus tears. The goal is to see if this tool can reduce pain and speed up recovery compared to the standard method. The NanoScope is part of a new generation of minimally invasive surgical tools that do not require standard incisions or portals.
Who is the study for?
This trial is for individuals with confirmed meniscus tears, shown by MRI, who have enough joint space and are undergoing their first knee arthroscopy. It's not for those over 60, on workers' compensation, or needing revision surgeries.
What is being tested?
The study compares two surgical methods for treating meniscus tears: a newer technique using a smaller Nanoscope and the traditional standard arthroscopic surgery. The goal is to see if the Nanoscope leads to less pain and quicker recovery.
What are the potential side effects?
While specific side effects aren't listed, typical risks of meniscectomy include pain at the incision site, swelling, infection risk, blood clots in legs or lungs (rare), and potential complications from anesthesia.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 hours
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Functional Outcomes Following Partial Meniscectomy: International Knee Documentation Committee Score
Functional Outcomes following partial meniscectomy: Knee Injury and Osteoarthritis Score
Secondary study objectives
Narcotic Medication Use
Pain: Visual Analog Pain Score
Return to work
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Nanoscopic Partial MeniscectomyExperimental Treatment1 Intervention
This is the experimental group. patients will have a partial meniscectomy performed using the arthrex nanoscope
Group II: Standard Partial MeniscectomyActive Control1 Intervention
Patients will have a partial meniscectomy performed using standard arthroscopic equipment which is the current gold standard
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for meniscus tears include conservative management (rest, physical therapy, and anti-inflammatory medications) and surgical interventions such as partial meniscectomy. The Nanoscope for Partial Meniscectomy is a minimally invasive surgical technique that uses a smaller diameter scope to remove the damaged meniscal tissue.
This approach aims to reduce pain and improve function by preserving as much of the healthy meniscus as possible, which is crucial for maintaining knee stability and function. Understanding these mechanisms helps patients appreciate the benefits of minimally invasive techniques, such as faster recovery times, reduced pain, and lower risk of complications compared to traditional arthroscopy.
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Who is running the clinical trial?
Marshall UniversityLead Sponsor
20 Previous Clinical Trials
4,062 Total Patients Enrolled
Medstar Washington Hospital CenterUNKNOWN
2 Previous Clinical Trials
3,400 Total Patients Enrolled
Arthrex, Inc.Industry Sponsor
46 Previous Clinical Trials
29,872 Total Patients Enrolled
1 Trials studying Meniscus Tears
50 Patients Enrolled for Meniscus Tears
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Nanoscopic Partial Meniscectomy
- Group 2: Standard Partial Meniscectomy
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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