- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07626983
Botulinum Toxin Type A Versus Local Anesthetic Injection for Chronic Neuroma Pain After Combat-Related Amputation (NEUROQUIET)
Botulinum Toxin Type A Versus Local Anesthetic Injection for Chronic Neuroma Pain After Combat-Related Amputation: A Multicenter Randomized Double-Blind Trial
Patients with combat-related amputations frequently experience persistent neuroma pain that may interfere with rehabilitation, prosthesis use, sleep, mobility, and quality of life. Current treatment options often provide only temporary relief. This study aims to compare two ultrasound-guided injection approaches for chronic neuroma pain after combat-related amputation: botulinum toxin type A and local anesthetic injection.
Participants will be randomly assigned to receive one of the two treatments. Pain intensity, neuropathic pain symptoms, phantom limb pain, prosthesis tolerance, and functional outcomes will be evaluated during follow-up visits over a 24-week period.
The goal of the study is to determine whether botulinum toxin type A provides longer-lasting pain reduction and improved functional recovery compared with local anesthetic injection in patients with chronic neuroma pain after combat-related amputation.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
Neuroma pain is a common and disabling complication after combat-related limb amputation. Persistent neuroma pain may contribute to residual limb pain, phantom limb pain, impaired prosthesis tolerance, sleep disturbance, reduced mobility, and decreased quality of life. Conventional treatment strategies, including local anesthetic injections, often provide only temporary pain relief.
Botulinum toxin type A has emerged as a potential treatment option because of its ability to modulate peripheral nociceptive signaling, reduce neurogenic inflammation, and decrease peripheral sensitization. However, evidence regarding its efficacy in patients with combat-related amputations remains limited.
The NEUROQUIET Trial is a multicenter, randomized, double-blind clinical trial designed to compare ultrasound-guided botulinum toxin type A injection versus ultrasound-guided local anesthetic injection for persistent neuroma pain after combat-related amputation.
Eligible participants with ultrasound-confirmed painful neuroma will be randomized in a 1:1 ratio to receive either botulinum toxin type A or local anesthetic injection under ultrasound guidance. Participants, outcome assessors, and data analysts will remain blinded to treatment allocation.
Patients will undergo longitudinal follow-up for 24 weeks. Outcomes will include pain intensity, neuropathic pain characteristics, phantom limb pain, residual limb pain, prosthesis tolerance, analgesic consumption, sleep disturbance, and patient-reported global improvement.
The study aims to determine whether botulinum toxin type A provides greater and longer-lasting analgesia compared with local anesthetic injection in patients with chronic neuroma pain following combat-related amputation.
Studietype
Registrering (Antatt)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiekontakt
- Navn: Dmytro Dmytriiev, PhD.Professor
- Telefonnummer: +380674309449
- E-post: mddmytriiev@gmail.com
Studiesteder
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Vinnitsa, Ukraina, 21000
- Vinnitsya university hospital
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Ta kontakt med:
- Dmytro Dmytriiev, Phd
- Telefonnummer: 0674309449
- E-post: mddmytriiev@gmail.com
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Vinnytsia Oblast
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Kyiv, Vinnytsia Oblast, Ukraina, 03143
- Feofaniya Clinical Hospital
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Ta kontakt med:
- Andrii Khomenko, MD
- Telefonnummer: +380937635858
- E-post: farmen@ukr.net
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
Tar imot friske frivillige
Beskrivelse
Inclusion Criteria:
- Age ≥18 years
- Combat-related limb amputation
- Persistent neuroma pain lasting ≥3 months
- Ultrasound-confirmed neuroma
- Positive Tinel sign over the neuroma
- Average pain intensity ≥4/10 on the Numeric Rating Scale (NRS)
- Stable analgesic regimen for at least 14 days before enrollment
- Ability to provide written informed consent
Exclusion Criteria:
- Active infection at the injection site
- Previous botulinum toxin injection within 6 months
- Previous neuroma surgery within 3 months
- Severe uncontrolled psychiatric disorder
- Coagulopathy or anticoagulant therapy contraindicating injection
- Known allergy to botulinum toxin or local anesthetics
- Severe uncontrolled systemic disease
- Inability to complete study follow-up or questionnaires
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Botulinum Toxin Type A
Ultrasound-guided perineuroma injection of botulinum toxin type A for persistent neuroma pain after combat-related amputation.
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Ultrasound-guided perineuroma injection of botulinum toxin type A for treatment of persistent neuroma pain after combat-related amputation.
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Aktiv komparator: Local Anesthetic
Ultrasound-guided perineuroma injection of local anesthetic for persistent neuroma pain after combat-related amputation.
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Ultrasound-guided perineuroma injection of local anesthetic for treatment of persistent neuroma pain after combat-related amputation.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Change in neuroma pain intensity measured
Tidsramme: Baseline to 12 weeks after intervention
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Assessment of change in average neuroma pain intensity using an 11-point Numeric Rating Scale (0 = no pain, 10 = worst imaginable pain) following ultrasound-guided injection treatment.
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Baseline to 12 weeks after intervention
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Residual Limb Pain Intensity Assessed Using the Numeric Rating Scale (NRS)
Tidsramme: Baseline to 24 weeks
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Residual limb pain intensity will be assessed using the 11-point Numeric Rating Scale (NRS). Participants will rate their average residual limb pain during the previous 7 days on a scale from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst imaginable pain." Higher scores indicate greater pain intensity and a worse clinical outcome. Scale Information: Numeric Rating Scale (NRS) Minimum Value: 0 Maximum Value: 10 Interpretation: Higher scores indicate worse residual limb pain intensity. |
Baseline to 24 weeks
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Pain Catastrophizing
Tidsramme: Baseline, 3 months, 6 months, and 12 months after amputation.
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Pain catastrophizing will be assessed using the Pain Catastrophizing Scale (PCS), a validated 13-item self-report questionnaire designed to measure catastrophic thinking related to pain. The PCS evaluates three domains: rumination, magnification, and helplessness. Total scores range from 0 to 52, with higher scores indicating greater levels of pain catastrophizing and a worse psychological pain profile. Scale Information: Pain Catastrophizing Scale (PCS) Minimum Value: 0 Maximum Value: 52 Interpretation: Higher scores indicate greater pain catastrophizing and worse pain-related psychological outcomes. |
Baseline, 3 months, 6 months, and 12 months after amputation.
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Prosthesis Tolerance Assessed Using the Prosthesis Evaluation Questionnaire (PEQ) - Utility and Satisfaction Domains
Tidsramme: Baseline to 24 weeks
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Prosthesis tolerance will be assessed using selected domains of the Prosthesis Evaluation Questionnaire (PEQ), a validated instrument evaluating comfort, utility, satisfaction, and functional use of the prosthesis. Scores range from 0 to 100, with higher scores indicating better prosthesis tolerance and satisfaction. Scale Information: Prosthesis Evaluation Questionnaire (PEQ) Minimum Value: 0 Maximum Value: 100 Interpretation: Higher scores indicate better prosthesis tolerance, comfort, and prosthetic adaptation. |
Baseline to 24 weeks
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Analgesic Consumption
Tidsramme: Baseline to 24 weeks
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Analgesic consumption will be assessed by calculating the total daily analgesic use and converting opioid medications into Oral Morphine Equivalent Daily Dose (OMEDD). Non-opioid analgesics (e.g., acetaminophen, NSAIDs, gabapentinoids) will also be recorded. Higher opioid consumption indicates greater analgesic requirements and potentially more severe pain. Measurement: Oral Morphine Equivalent Daily Dose (OMEDD), expressed in milligrams per day (mg/day) Minimum Value: 0 mg/day Maximum Value: No predefined maximum value Interpretation: Higher values indicate greater analgesic consumption and higher pain management requirements. |
Baseline to 24 weeks
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Patient Global Impression of Change (PGIC)
Tidsramme: Week 12 and Week 24
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Overall perceived improvement will be assessed using the Patient Global Impression of Change (PGIC) scale. The PGIC is a validated patient-reported outcome measure that evaluates a participant's perception of change in pain, function, and overall health status since the beginning of treatment. Participants rate their overall improvement on a 7-point scale ranging from "Very much worse" to "Very much improved." Scale Information: Patient Global Impression of Change (PGIC) Minimum Value: 1 (Very much worse) Maximum Value: 7 (Very much improved) Interpretation: Higher scores indicate greater perceived improvement and better overall clinical outcomes. Scale Categories:
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Week 12 and Week 24
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Adverse Events
Tidsramme: Baseline to 24 weeks
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Adverse events will be assessed by recording the occurrence, type, severity, and relationship to treatment throughout the study period. Events may include medication-related adverse effects, prosthesis-related complications, falls, skin breakdown, residual limb complications, infections, hospitalizations, and other clinically significant events. Severity will be graded according to the Common Terminology Criteria for Adverse Events (CTCAE), Version 5.0, when applicable. Measurement: Number of participants experiencing one or more adverse events. Minimum Value: 0 participants Maximum Value: Number of participants enrolled in the study Interpretation: Higher values indicate a greater incidence of adverse events and worse safety outcomes. Additional Safety Assessment: Severity of adverse events will be categorized as Grade 1 (Mild) to Grade 5 (Death related to adverse event) according to CTCAE v5.0. |
Baseline to 24 weeks
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Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Sleep Disturbance
Tidsramme: Baseline to 24 weeks
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Sleep disturbance will be assessed using the Pittsburgh Sleep Quality Index (PSQI), a validated 19-item questionnaire that evaluates subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleep medication, and daytime dysfunction during the previous month. The global PSQI score ranges from 0 to 21, with higher scores indicating poorer sleep quality and greater sleep disturbance. Scale Information: Pittsburgh Sleep Quality Index (PSQI) Minimum Value: 0 Maximum Value: 21 Interpretation: Higher scores indicate worse sleep quality and greater sleep disturbance. Clinical Interpretation: A global PSQI score >5 is commonly considered indicative of clinically significant sleep disturbance. |
Baseline to 24 weeks
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Functional Mobility
Tidsramme: Baseline to 24 weeks
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Functional mobility will be assessed using the Amputee Mobility Predictor (AMP), a validated performance-based instrument designed to evaluate ambulatory potential, balance, transfers, gait, and functional mobility in individuals with lower-limb amputation. The scale assesses the patient's ability to perform a series of mobility tasks and predicts prosthetic functional potential. Scale Information: Amputee Mobility Predictor (AMP) Minimum Value: 0 Maximum Value: 47 Interpretation: Higher scores indicate better functional mobility, greater ambulatory capacity, and improved rehabilitation outcomes. Clinical Interpretation: Higher AMP scores are associated with higher functional levels and greater potential for successful prosthetic use. |
Baseline to 24 weeks
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Need for Repeat Intervention
Tidsramme: Up to 24 weeks
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he need for repeat intervention will be assessed by recording the number of participants who require additional pain-related interventions following the initial treatment. Repeat interventions may include repeat nerve blocks, cryoneurolysis, radiofrequency ablation, neuroma surgery, revision procedures, additional injections, or other clinically indicated pain-management procedures. Measurement: Number of participants requiring one or more additional pain-related interventions during follow-up. Minimum Value: 0 participants Maximum Value: Number of participants enrolled in the study Interpretation: Higher values indicate a greater need for additional interventions and may reflect reduced durability or effectiveness of the initial treatment. Additional Analysis: Time to first repeat intervention (days) may also be recorded and analyzed as a secondary outcome. |
Up to 24 weeks
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Patient Satisfaction
Tidsramme: Week 12 and Week 24
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Patient satisfaction will be assessed using the Client Satisfaction Questionnaire (CSQ-8), a validated 8-item patient-reported outcome measure evaluating satisfaction with treatment, services received, and overall care experience. Total scores range from 8 to 32, with higher scores indicating greater satisfaction with treatment outcomes and care. Scale Information: Client Satisfaction Questionnaire (CSQ-8) Minimum Value: 8 Maximum Value: 32 Interpretation: Higher scores indicate greater patient satisfaction and better perceived treatment outcomes. |
Week 12 and Week 24
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Neuroma Maximum Diameter Measured by High-Resolution Ultrasound
Tidsramme: Baseline and Week 24
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Neuroma size will be assessed using high-resolution ultrasound. The maximum neuroma diameter will be measured in the longitudinal or transverse plane and recorded in millimeters (mm). The largest measured diameter will be used for analysis. Unit of Measure: Millimeters (mm) Minimum Value: 0 mm Maximum Value: No predefined maximum value Interpretation: Higher values indicate larger neuroma size and greater structural abnormality. |
Baseline and Week 24
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Samarbeidspartnere og etterforskere
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Smerte
- Nevrologiske manifestasjoner
- Sykdommer i nervesystemet
- Postoperative komplikasjoner
- Patologiske prosesser
- Nevromuskulære sykdommer
- Sykdommer i det perifere nervesystemet
- Nevroatferdsmanifestasjoner
- Perseptuelle forstyrrelser
- Smerter, postoperativt
- Patologiske tilstander, tegn og symptomer
- Tegn og symptomer
- Nevralgi
- Fantomlem
- Aminosyrer, peptider og proteiner
- Proteiner
- Biologiske faktorer
- Hydrolaser
- Enzymer
- Enzymer og koenzymer
- Botulinumtoksiner
- Metalloendopeptidaser
- Endopeptidaser
- Peptidhydrolaser
- Metalloproteaser
- Bakterielle proteiner
- Bakterielle giftstoffer
- Giftstoffer, biologisk
- Botulinumtoksiner, type A
- incobotulinumtoxinA
Andre studie-ID-numre
- 2205v0123052026
- UARA-NEUROQUIET (Annen identifikator: UARA-NEUROQUIET)
Plan for individuelle deltakerdata (IPD)
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IPD-planbeskrivelse
IPD-delingstidsramme
Tilgangskriterier for IPD-deling
IPD-deling Støtteinformasjonstype
- STUDY_PROTOCOL
- SEVJE
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