A study on efficacy of Pregabalin for the cervical dissection postoperative pai
Not Applicable
- Conditions
- cervical dissection postoperative pain
- Registration Number
- JPRN-UMIN000005479
- Lead Sponsor
- Okayama University Hospital,Department of Otolaryngology-Head and Neck surgery
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
(1) the patients with a history of hypersensitivity for an ingredient of pregabalin. (2) A pregnant woman, woman in childbed, nursing mother. (3) The serum creatinine level is the patients more than 0.9 mg/dl.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Subjective improvement (VAS level) with pregabalin of the cervical dissection postoperative pain
- Secondary Outcome Measures
Name Time Method After improvement (PDAS score) of the quality of life with the pregabalin administration, neck dissection a change of the quality of life using the questionnaire (a simple version), improvement (a VAS level, THI, an examination for standard tinnitus) of the tinnitus with the pregabalin administration