Efficacy of Ultrasound-guided Injection of 5% Dextrose for Meralgia Paresthesia
- Conditions
- Meralgia Paresthetica
- Interventions
- Other: injection
- Registration Number
- NCT06251882
- Lead Sponsor
- Peking University People's Hospital
- Brief Summary
Meralgia paresthetica (MP) is one of the most common peripheral entrapment neuropathies of the lower limbs. It is characterized by paresthesia, pain, tingling, numbness, hypersensitivity, or other abnormal skin sensations on the anterolateral aspect of the thigh. The condition results from compression of the lateral femoral cutaneous nerve (LFCN) along its course, often occurring as the nerve exits the pelvis.The injection of 5% dextrose (D5W) under ultrasound guidance is a novel treatment method for peripheral nerve entrapment. However, there is limited evidence about the efficacy of this method for patients with MP. The investigators found D5W was more safe and effective than corticosteroids for patients with MP. Thus, this study aimed to evaluate the 6-month efficacy of ultrasound-guided injection of D5W for MP patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 40
- patients aged between 18 and 80 years;
- those diagnosed with MP based on clinical and physical examination, with symptoms persisting for at least 3 months;
- a high-resolution ultrasound revealing LFCN compression as it exited the pelvis.
- MP resulting from trauma, surgery or occupying lesions affecting the LFCN;
- pregnancy;
- concurrent presence of rheumatic immune diseases, hypothyroidism, or diabetes mellitus;
- a known history of allergy to lidocaine or corticosteroids;
- L2/3 lumbar radiculopathy;
- patients who had undergone local injection or surgery for MP within 3 months
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description D5W group injection The patients received one session of ultrasound-guided 10ml D5W injection around the lateral femoral cutaneous nerve as it exited the pelvis.
- Primary Outcome Measures
Name Time Method visual analogue scale(VAS) baseline as well as 1month, 3 month, 6 months post-injection VAS is one of the most common tool to assess pain severity for patients, ranging from 0(no pain) to 10(most possible pain).
- Secondary Outcome Measures
Name Time Method cross-sectional area(CSA) of the nerve baseline as well as 1month, 3 month, 6 months post-injection CSA could reflect the compression of the nerve, to some extent
Trial Locations
- Locations (1)
Peking University People's Hospital
🇨🇳Beijing, Beijing, China