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Preoperative Gabapentine for Carpal Tunnel

F

Federal University of São Paulo

Status and phase

Completed
Phase 3

Conditions

Carpal Tunnel Syndrome

Treatments

Other: Sugar pill
Drug: Gabapentine

Study type

Interventional

Funder types

Other

Identifiers

NCT01632215
CEP 0223/09

Details and patient eligibility

About

The purpose of this study was to evaluate the postoperative analgesic effect of preoperative gabapentine for carpal tunnel syndrome surgery.

Full description

There was studied 40 patients. Group 1 patients received 600 mg of gabapentin 1 hour before surgery; G2 received placebo 1 hour before surgery.

Anesthesia was regional intravenous block. Postoperative analgesia when needed was with acetaminophen. If needed was administered codeine. The evaluation of neuropathic pain was made by DN4 questionnaire. Pain intensity was assessed by numeric scale at block and after 30min, 1h, 2h, 2wk, 4wk, 6m. It was noted the duration of analgesia, and the amount of acetaminophen and codeine.

The statistical program used for analysis of the results was the Instat Graph

Enrollment

40 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • carpal tunnel syndrome

Exclusion criteria

  • disorientation, psychiatric disease, myocardial ischemia, hypertension, arrhythmia, another pain syndrome, drug user, and pregnant

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

40 participants in 2 patient groups, including a placebo group

preoperative gabapentine,
Experimental group
Description:
Gabapentine
Treatment:
Drug: Gabapentine
sugar pill
Placebo Comparator group
Description:
Placebo group
Treatment:
Other: Sugar pill

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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