To evaluate the safety and efficacy of pregabalin in reducing neuropathic pain associated with HIV neuropathy
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
220
75mg BID, titrated up to 300mg according to individual response and tolerability
Mean Visual Analogue Scale (VAS) Pain Scores
Pain scores were assessed on a 100 mm Visual Analogue Scale (VAS); scores range from 0= no pain to 100= worse pain. Subjects assessed their pain during the last week. Endpoint = last non-missing observation carried forward after Baseline visit.
Time frame: Baseline, Week 4, Week 8, Week 12, and Endpoint
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