Gabapentin and Neural Mobilization Pain Reduction Effect Compared to Only Gabapentine
NCT ID: NCT06778798
Last Updated: 2025-12-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
72 participants
INTERVENTIONAL
2025-02-19
2025-03-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
TRIPLE
Study Groups
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Median nerve neural mobilization and oral gabapentin
Median nerve neural mobilization, non pharmaceutical, non invasive, physiotherapy technique; which consists of a passive and repetitive upper limb movement that seeks to induce median nerve gliding and incursions against surrounding connective tissue. Subjects will be treated 5 days per week during a total time lapse of 2 weeks. This arm will also receive a Gabapentin Oral capsule pharmaceutical treatment. Participants will be treated with a maximum of 600 mg per day, subdivided in 2 intakes of 300 mg each 12 hours during a time lapse of 2 weeks.
Median nerve neural mobilization and oral gabapentin
Manual therapy maneuver performed in the upper limb combined with gabapentin oral capsules.
Gabapentin
Gabapentin Oral capsule pharmaceutical treatment. Participants will be treated with a maximum of 600 mg per day, subdivided in 2 intakes of 300 mg each 12 hours during a time lapse of 2 weeks.
Gabapentin 300mg
Gabapentin oral capsules
Interventions
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Median nerve neural mobilization and oral gabapentin
Manual therapy maneuver performed in the upper limb combined with gabapentin oral capsules.
Gabapentin 300mg
Gabapentin oral capsules
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Full understanding of written and spoken Spanish (language).
* Participants must freely consent to participate.
* The presence of positive Phalen and Tinel signs.
* The presence of carpal tunnel syndrome signs and symptoms
Exclusion Criteria
18 Years
70 Years
ALL
Yes
Sponsors
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Universidad Europea de Madrid
OTHER
Responsible Party
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Francisco Unda Solano
Biomedicine Doctorate Program Investigator
Principal Investigators
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Francisco Unda, PhD
Role: PRINCIPAL_INVESTIGATOR
Locations
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Ciudad Hospitalaria Enrique Tejera
Valencia, Carabobo, Venezuela
Countries
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Other Identifiers
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CE0072015-02-06
Identifier Type: -
Identifier Source: org_study_id
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