About this trial

This is a study to establish a safe and feasible dose for prophylactic use of a combination of gabapentin and ketamine in head and neck cancer patients undergoing chemoradiation.

Eligibility criteria

Qualifiers

Histologically proven cancer of the head and neck cancer

Locally advanced non-metastatic disease (T3N0M0, T4N0M0, T1-4N1-3M0)

Planned primary or adjuvant radiation or chemoradiation therapy

Willing and able to provide informed consent

Disqualifiers

Currently on gabapentin or ketamine

Prior non-tolerance of gabapentin or ketamine

Unable to administer ketamine intranasally due to anatomical restrictions

History of seizure disorder

Trial design

Treatments tested in this trial

  • Gabapentin
  • Ketamine

Treatment groups

64 Participants
are divided into 1 treatment group

Locations

1
Vanderbilt-Ingram Cancer Center37232, NashvilleTennessee, United States

Sponsors and collaborators

Natalie Lockney

Lead sponsor

Vanderbilt-Ingram Cancer Center

Sponsor institution