Non-Contact Low-Frequency Ultrasound Vs Standard LaLonde Protocol for Fingertip Injury Wound Healing
Recruiting
N/A
Interventional Study
Non-contact Low Frequency Ultrasound
Lalonde Protocol
Fingertip Amputation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 22 (estimated)
- Sponsor
- St. Luke's Hospital, Pennsylvania · Other
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About This Trial
The goal of this clinical trial is to compare the efficacy of non-contact low frequency ultrasound in populations sustaining fingertip amputations. The main question it aims to answer is:
• Does non-contact low frequency ultrasound significantly improve patient outcomes in patients sustaining acute fingertip amputations?
Researchers will compare non-contact low frequency ultrasound to a standard…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Individuals aged 18 years or older with an acute traumatic fingertip amputation without exposed bone or tendons (Allen 1, Tamai level 1; ICD-10 codes S68.5 and S68.6).
Exclusion Criteria:
* Patients less than 18 years old,
* Injuries involving exposed bone
* Those with diagn…
Contacts