- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07625020
Ultrasound-Guided Nerve Hydrodissection for Diabetic Lower Limb Entrapment Neuropathy (HUND)
Ultrasound-Guided Nerve Hydrodissection for Diabetic Lower Limb Entrapment Neuropathy: A Randomized, Single-Blind, Sham-Controlled Trial
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiekontakt
- Navn: Qingfeng Cheng, PhD
- Telefonnummer: 13628482293
- E-mail: cqf19760516@163.com
Studiesteder
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Chongqing Municipality
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Chongqing, Chongqing Municipality, Kina, 400016
- Rekruttering
- The First Affiliated Hospital of Chongqing Medical University
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Kontakt:
- Qingfeng Cheng, PhD
- Telefonnummer: 13628482293
- E-mail: cqf19760516@163.com
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Age 18-85 years, male or female;
- Diagnosis of DLLEN meeting the following criteria: ① Clinical diagnosis of DPN (presence of DPN clinical symptoms plus at least one positive physical sign, or absence of symptoms but presence of two or more positive physical signs), with other etiologies excluded; ② Presence of unilateral or bilateral lower limb symptoms suggestive of peripheral nerve entrapment, including hypoesthesia/paresthesia in a specific nerve distribution area, pain and/or motor dysfunction, or a positive Tinel sign at the corresponding site; ③ Physical examination findings such as decreased or absent skin sensation in the corresponding nerve distribution area, reduced or absent strength of ankle dorsiflexion or eversion, metatarsophalangeal joint movement disorder, foot drop, or foot inversion; ④ Electrophysiological study showing slowing or blockade of nerve conduction velocity at a specific site (across a narrowed segment); ⑤ Imaging study (nerve ultrasound) showing compression of the corresponding nerve (cross-sectional area at the entrapment site exceeding the upper limit of the reference range, decreased nerve echogenicity, or swelling of the nerve fascicles). Diagnosis requires fulfillment of ①, ②, and ③, plus either ④ or ⑤;
- Inadequate response to adequate treatment with medications such as mecobalamin and α-lipoic acid;
- Understanding of the entire study process and voluntary provision of written informed consent.
Exclusion Criteria:
- Presence of another clearly identified etiology assessed by the investigator as the primary cause of the patient's current lower limb neurological symptoms, including but not limited to: cervical or lumbar spine disease (e.g., radicular symptoms or sciatica), lower extremity vascular disease, cerebral infarction, thyroid dysfunction, vitamin B12 deficiency, heavy alcohol use history, recent chemotherapy or radiotherapy, drug toxicity, or other non-diabetic causes of neuropathy (e.g., CIDP, cauda equina syndrome, subacute combined degeneration of the spinal cord, Guillain-Barré syndrome);
- Concurrent malignancy, active systemic infection, or immune system disease;
- Lower limb edema due to any cause;
- Skin breakdown or infection at the treatment site below the knee;
- Severe cardiac, hepatic, or renal insufficiency (eGFR <30 mL/min/1.73m², liver transaminases >2.5 times the upper limit of normal, or New York Heart Association functional class ≥II);
- Cognitive impairment or severe mental illness;
- Pregnancy or breastfeeding;
- Participation in another interventional clinical trial within the past 3 months;
- Poor compliance, assessed as unlikely to complete the study per protocol;
- Any other condition assessed by the investigator as making the patient unsuitable to complete the trial.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Ultrasound-guided nerve hydrodissection treatment group
The patient is placed in a standard position, followed by routine disinfection and draping.
A high-frequency ultrasound probe is used and covered with a sterile sheath to clearly visualize the target nerve.
Using an in-plane puncture technique, the needle tip is advanced to the perineural fascial plane under real-time guidance.
After confirming placement and negative aspiration, a pre-prepared solution of mecobalamin and normal saline is slowly injected.
The main sites are the common peroneal nerve (fibular head) and tibial nerve (medial malleolus).
Based on preliminary data, a volume of 20 mL is injected, which separates the nerve from surrounding tissues without causing significant discomfort.
The fixed volume ensures a standardized procedure.
During injection, fluid spread is monitored to ensure it surrounds the nerve and achieves hydrodissection.
After injection, the needle is withdrawn, local compression is applied, and the site is covered with a sterile dressing.
|
The patient is placed in a standard position, followed by routine disinfection and draping.
A high-frequency ultrasound probe is used and covered with a sterile sheath to clearly visualize the target nerve.
Using an in-plane puncture technique, the needle tip is advanced to the perineural fascial plane under real-time guidance.
After confirming placement and negative aspiration, a pre-prepared solution of mecobalamin and normal saline is slowly injected.
The main sites are the common peroneal nerve (fibular head) and tibial nerve (medial malleolus).
Based on preliminary data, a volume of 20 mL is injected, which separates the nerve from surrounding tissues without causing significant discomfort.
The fixed volume ensures a standardized procedure.
During injection, fluid spread is monitored to ensure it surrounds the nerve and achieves hydrodissection.
After injection, the needle is withdrawn, local compression is applied, and the site is covered with a sterile dressing.
Andre navne:
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Sham-komparator: Sham treatment group
The patient is placed in the same standard position, followed by identical disinfection and ultrasound positioning.
Under ultrasound guidance, a needle identical in appearance is inserted into the superficial subcutaneous fascia above the target nerve, clearly avoiding the nerve structure.
A syringe containing mecobalamin and normal saline is then connected, and a full set of simulated injection maneuvers including aspiration and slow "injection" is performed, while ensuring that the actual volume of fluid delivered is small (less than 5 mL).
To simulate a real sensory experience, the operator provides standardized verbal cues during the procedure.
After needle withdrawal, local compression and dressing application are performed identically to the treatment group.
|
The patient is placed in the same standard position, followed by identical disinfection and ultrasound positioning.
Under ultrasound guidance, a needle identical in appearance is inserted into the superficial subcutaneous fascia above the target nerve, clearly avoiding the nerve structure.
A syringe containing mecobalamin and normal saline is then connected, and a full set of simulated injection maneuvers including aspiration and slow "injection" is performed, while ensuring that the actual volume of fluid delivered is small (less than 5 mL).
To simulate a real sensory experience, the operator provides standardized verbal cues during the procedure.
After needle withdrawal, local compression and dressing application are performed identically to the treatment group.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Remission rate of TCSS score
Tidsramme: At 1 month after the treatment
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The Toronto Clinical Scoring System (TCSS) assesses neuropathy symptoms, sensory deficits, and reflexes, with a total score ranging from 0 to 19. Higher scores indicate worse outcomes (more severe neuropathy). Remission is defined as a decrease of 1 point or more from baseline. This outcome is compared between the ultrasound-guided nerve hydrodissection group and the sham treatment group. |
At 1 month after the treatment
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Change in TCSS from baseline
Tidsramme: Within 5 days and 1 month after the treatment
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Changes in TCSS from baseline
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Within 5 days and 1 month after the treatment
|
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Change in ultrasound-measured nerve cross-sectional area (CSA) from baseline
Tidsramme: At 1 month after the treatment
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Changes in nerve cross-sectional area measured by ultrasound compared to baseline
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At 1 month after the treatment
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Changes in each component of TCSS compared to baseline
Tidsramme: Within 5 days and 1 month after the treatment
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Changes in each component of the Toronto Clinical Scoring System (TCSS) from baseline. The TCSS assesses three components: symptoms, sensory deficits, and reflexes. Total score range: 0 to 19 Each component has its own sub-score range (symptoms: 0-6, sensory: 0-5, reflexes: 0-8) Higher scores indicate worse outcomes (more severe neuropathy) This outcome measures the within-group change from baseline at each follow-up time point. |
Within 5 days and 1 month after the treatment
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Change in VAS pain score from baseline
Tidsramme: Within 5 days and 1 month after the treatment
|
Visual Analogue scale(VAS)Score range: 0-10 Higher scores indicate worse outcomes (more severe pain) This outcome measures the within-group change from baseline at each follow-up time point. |
Within 5 days and 1 month after the treatment
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Change in EQ-5D quality of life score from baseline
Tidsramme: Within 5 days and 1 month after the treatment
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Changes in the EuroQol Five-Dimensional Five-Level Questionnaire (EQ-5D-5L) from baseline. The EQ-5D-5L consists of two components:
Self-rated overall health on a vertical scale Score range: 0 (worst imaginable health) to 100 (best imaginable health) Higher scores indicate better outcomes This outcome measures the within-group change from baseline at each follow-up time point. |
Within 5 days and 1 month after the treatment
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Patient Global Impression of Change (PGIC)
Tidsramme: Within 5 days and 1 month after the treatment
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Patients' self-assessment of overall change in their condition since the start of treatment, measured by the Patient Global Impression of Change (PGIC) scale. The PGIC is a 7-point rating scale: Score range: 1 to 7 Scoring:
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Within 5 days and 1 month after the treatment
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Samarbejdspartnere og efterforskere
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Sygdomme i nervesystemet
- Neuromuskulære sygdomme
- Genetiske sygdomme, medfødte
- Sygdomme i det perifere nervesystem
- Neurodegenerative sygdomme
- Medfødte abnormiteter
- Heredodegenerative lidelser, nervesystem
- Misdannelser i nervesystemet
- Polyneuropatier
- Arvelig sensorisk og motorisk neuropati
- Medfødte, arvelige og neonatale sygdomme og abnormiteter
- Charcot-Marie-Tooth sygdom
Andre undersøgelses-id-numre
- 2026-0264-02
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