A study on efficacy of Pregabalin for the cervical dissection postoperative pain

A study on efficacy of Pregabalin for the cervical dissection postoperative pain - cervical dissection postoperative pain

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000005479

Enrollment

Registered

2011-04-25

Start date

2011-04-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

cervical dissection postoperative pain

Interventions

pregabalin NSAIDS,Fomentation,and othors

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: After cervical dissection enforcement, pass more than 30 days; the patients with the pain after the cervical dissection

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Subjective improvement (VAS level) with pregabalin of the cervical dissection postoperative pain	—

Secondary

Measure	Time frame
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	—

Countries

Japan

Contacts

Public ContactTomoo Onoda

Okayama University Hospital Department of Otolaryngology-Head and Neck surgery

0862357307

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026