Observational Study of Allay™ Hydrogel Cap for Peripheral Nerve Injuries
This study is observing the safety and effectiveness of the allay™ Hydrogel Cap, a device used during nerve surgeries like amputations or neuroma excisions (removal of nerve tumors). We are looking at patients who have already received or will receive the allay™ Hydrogel Cap. The main goal is to see how well the cap works by tracking changes in your pain levels, how much pain interferes with your daily life, and if you experience cold intolerance. We'll also look at whether neuromas return and how your pain medication use changes over time. This study aims to gather information from 1000 participants.
- Study design
- This is an observational study, meaning we will collect information from patients who receive the allay™ Hydrogel Cap. It is open-label, so everyone involved will know you are receiving the device.
- What's involved
- You would provide information at baseline (before surgery), and then at 2 weeks, 1 month, 4 months, 12 months, and 24 months after surgery.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for up to 24 months (2 years) after their surgery.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Continuous Observational Monitoring Program for Allay™ Hydrogel Cap Safety and Success Study
At a glance
Conditions
NCT07246980
Where you'd take part
This study runs at 4 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Complete Foot and Ankle Care of North Texas, PA
Denton, Texasstudy coordinator listed
Recruiting
Florida Orthopedic Institute
St. Petersburg, Floridastudy coordinator listed
Recruiting
Orlando Health
Orlando, Floridastudy coordinator listed
Recruiting
University of Colorado Anschutz.
Englewood, Coloradostudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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What this trial measures
- Assessment of change in Pain Scores from baseline using VASBaseline (Pre Surgery ), 2 Weeks, 1 month, 4 month, 12 month and 24 month (Post Surgery)
Pain scores will be collected using either of the following scales: 1\) The Visual Analog Scale (VAS) or 2) The Numerical Rating Scale (NRS) The VAS for pain is a simple, validated tool used to measure a patient's perceived pain intensity. It consists of a straight 100 mm horizontal line labeled from "no pain" (0) on the left to "worst imaginable pain" (100) on the right. Patients are asked to mark a point on the line that corresponds to their current level of pain, which is then measured in millimeters from the zero point to quantify the score. The VAS is widely used in both clinical and research settings due to its ease of use and sensitivity to changes in pain over time.
- Assessment of change in Pain scores from baseline using Numerical Rating ScaleBaseline (Pre Surgery ), 2 Weeks, 1 month, 4 month, 12 month and 24 month (Post Surgery)
The NRS is a validated pain screening tool, commonly used to assess pain severity at that moment in time using a 0-10 scale, with zero meaning "no pain" and 10 meaning "the worst pain imaginable. The patient selects the single whole number that best reflects how severe their current pain is to them.
- Assessment of change in Pain Interference from baseline using PROMIS PI Short Form 5bBaseline (Pre Surgery ), 2 Weeks, 1 month, 4 month, 12 month and 24 month (Post Surgery)
The Patient-Reported Outcomes Measurement Information System Pain Interference (PROMIS-PI) scale is a validated tool used to assess the extent to which pain hinders engagement with social, cognitive, emotional, physical, and recreational activities. It measures the impact of pain over the past seven days using a series of standardized questions rated on a 5-point Likert scale. Scores are converted to T-scores, with higher scores indicating greater pain interference. The PROMIS-PI is widely used in clinical research due to its reliability, responsiveness, and ability to compare results across diverse patient populations.
- Assessment of change in Neuropathic Pain Quality from baseline using Patient-Reported Outcome Measurement Information System (PROMIS) v2.0 Neuropathic Pain Quality 5aBaseline (Pre Surgery ), 2 Weeks, 1 month, 4 month, 12 month and 24 month (Post Surgery)
The Patient-Reported Outcome Measurement Information System (PROMIS) v2.0 Neuropathic Pain Quality 5a is a 5-item, self-administered questionnaire for participants to assess qualities of neuropathic pain, like "numb," "tingly," and "shooting," over the past seven(7) days. The final score is represented by the T-score, a standardized score with a mean of 50 and a standard deviation (SD) of 10. Higher T-scores indicate more severe neuropathic pain. It helps to accurately screen for neuropathic pain, which arises from nerve damage, versus nociceptive pain, which comes from tissue injury, and can then assess the severity of the condition.
- Assessment of change in Cold Intolerance from baseline using Cold Intolerance Symptom Severity (CISS) scoreBaseline (Pre Surgery ), 2 Weeks, 1 month, 4 month, 12 month and 24 month (Post Surgery)
The Cold Intolerance Symptom Severity (CISS) score is a validated patient-reported outcome measure used to assess the severity of cold intolerance, often following peripheral nerve injury or extremity trauma. The questionnaire includes six items evaluating symptoms such as pain, numbness, stiffness, color changes, and the impact on daily activities in response to cold exposure. Each item is scored on a Likert scale, with the total score ranging from 4 to 100, where higher scores indicate greater symptom severity. The CISS is commonly used in clinical research to quantify cold intolerance and monitor changes over time or in response to interventions.
- Assessment of change from baseline in the average quantity of pain medication taken via the Medication Quantification Scale (MQS) at 12 months.Baseline (Pre Surgery ), 2 Weeks, 1 month, 4 month, 12 months (Post Surgery)
A pain medication log will be provided to each participant to complete at all visits. For opioid and non-opioid pain medications, the Medication Quantification Scale (MQS) Version III is a validated tool used to quantify the complexity and detriment of pain medication regimens. It calculates a single numeric value by combining medication detriment weights (ranging from 1.1 to 4.5) with dosage levels (scaled from 1 for subtherapeutic use to 4 for supratherapeutic use). A higher MQS score indicates greater potential medication detriment and/or dosage intensity. At 12 months, the study assessed changes from baseline in patients' average MQS scores.