Post-traumatic neuropathy from facial fracture Gabapentin, Neuropathy, Facial fracture, Sensory impairment, Pain intensity, Quality of life
Conditions
Interventions
Received Gabapentin(300mg) 1 tab per oral twice a day for 3 months,Received Vitamin B 1 tab per oral twice a day for 3 months
Gabapentin,Vitamin B
Sponsors
Faculty of Medicine Siriraj Hospital, Mahidol University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Traumatic facial fracture patient who in stable condition, 2. Numbness at fracture site, 3. First visit at facial fracture clinic within 2 weeks after injuries
Exclusion criteria
Exclusion criteria: 1. Who has other injuries that interfere assessment, 2. Who has Intellectual disability or Communication disability, 3. Who are pregnancy or lactation, 4. Who allergic to gabapentin, 5. Who is using Gabapentin, Carbamazepine, Amitriptyline, 6. Who is recieved surgery from the fracture, 7. End stage kidney disease (CrCl < 15 ml/min ), 8. Who has history of analgesic drus abuse
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Neuropathy at 3 months after end of the intervention level of sensory impairment,Neuropathy at 3 months after end of the intervention pain intensity | — |
Secondary
| Measure | Time frame |
|---|---|
| Sensation at 3 months after end of the intervention Patient reported outcome using a questionnaire interview,adverse event at 3 months after end of the intervention Patient reported outcome using a questionnaire interview,discontinuation at 3 months after end of the intervention Patient reported outcome using a questionnaire interview,satisfaction at 3 months after end of the intervention Patient reported outcome using a questionnaire interview,quality of life at 3 months after end of the intervention Patient reported outcome using a questionnaire interview | — |
Countries
Thailand
Contacts
Public ContactJatuporn Sirikun
Department of surgery, Faculty of medicine, Siriraj Hospital
Outcome results
None listed