Clinical Trial Details
Braintumor Website

[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT03610763 : Harnessing Neuroplasticity to Enhance Functional Recovery During Chronic Recovery From Upper Extremity Nerve Repair
PhaseN/A
AgesMin: 18 Years Max: N/A
Eligibility
Inclusion Criteria:

- Individuals whom have received a unilateral allogeneic transplantation proximal to the
wrist and are at the chronic stage of recovery (approx. 12 - 18 months following
surgery, when Tinel's sign reaches the distal fingertips).

- Individuals whom have undergone a complete amputation the hand between the wrist and
elbow followed by successful re-attachment and are at the chronic stage of recovery
(approx. 12 - 18 months following surgery, when Tinel's sign reaches the distal
fingertips).

- Individuals whom have undergone repairs of the median, ulnar, or other related or
nearby nerve(s) following complex volar forearm lacerations or other injuries between
the distal wrist crease and the flexor musculotendinous junctions. Individuals must be
at the chronic stage of recovery (approx. 12 - 18 months following surgery, when
Tinel's sign reaches the distal fingertips).

Exclusion Criteria:

- Individuals with significant/severe brain trauma

- Serious psychiatric conditions

- Chronic or severe neurological conditions.

- Current pregnancy

- History of seizures or unexplained loss of consciousness

- Metallic implants above the chest

- Certain implanted medical devices.
LinksPermanent Link to THIS page: https://virtualtrials.com/nct/display1trial.cfm?nct=NCT03610763      |      Link to official Clinicaltrials.gov listing
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