Nerve Pain After Surgery

  • STATUS
    Recruiting
  • sponsor
    Averitas
Updated on 2 September 2021

Summary

A clinical trial evaluating the efficacy and safety of the topical study medication in subjects with post-surgical neuropathic pain.

Description

The purpose of this study is to evaluate the efficacy and safety of the medication in subjects with post-surgical neuropathic pain. The study may last up to 44 weeks.

Details
Condition Post-Surgical Pain, post-surgical neuropathic pain
Clinical Study IdentifierTX281509
SponsorAveritas
Last Modified on2 September 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Female or male subjects aged 18 years or older
A history of post-surgical pain with a duration of at least 6 months to maximally 36 months that is plausibly related to the surgical intervention

Exclusion Criteria

Neuropathic pain areas located only on the face, above the hairline of the scalp, and/or in proximity to mucous membranes
Pending litigation due to chronic pain or disability
The subject has a history of alcohol or drug abuse or is actively abusing drugs (including alcohol, medication) during the 1 year prior to the Screening Visit
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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