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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03051113
Other study ID # NeuromUL2016
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2016
Est. completion date December 2018

Study information

Verified date February 2019
Source Danish Pain Research Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Neuromas are frequent after trauma and surgery, including amputation and can be identified by high-resolution ultrasound. The role of neuromas as the cause of neuropathic pain is uncertain. In this observational cohort study, the investigators wish to explore if the prevalence of neuromas are higher in patients with pain after peripheral nerve injury and amputation, than in patients with the same conditions but without pain.


Recruitment information / eligibility

Status Completed
Enrollment 67
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Subjects with peripheral nerve injury 3 months prior to participation

- Subjects with amputation 3 months or more prior to participation

Exclusion Criteria:

- Severe somatic or psychiatric diseases

- Other peripheral neuropathy

- Lack of ability to cooperate to the clinical examination

Study Design


Locations

Country Name City State
Denmark Danish Pain Research Center, Aarhus University Hospital Aarhus

Sponsors (1)

Lead Sponsor Collaborator
Danish Pain Research Center

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of neuromas in patients with pain and without pain after peripheral nerve injury or amputation. Neuromas identified by ultrasound. 3 hours
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