Pilot Study of Management of Facial Paralysis in the Oncologic Patient: Nerve Transfer Techniques to Improve Facial Function and Quality of Life

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this research study is to measure changes in patients' quality of life after surgeries that affect the facial nerve, including nerve transfer as treatment for facial paralysis.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ In order to be eligible to participate in the intervention group of this study, an individual must meet all of the following criteria:

• Provision of signed and dated informed consent form

• Aged 18 or greater

• Patient scheduled to undergo facial nerve transfer

• Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study

⁃ In order to be eligible to participate in the non-intervention historical control group of this study, an individual must meet all of the following criteria:

• Provision of signed and dated informed consent form

• Aged 18 or greater

• Previous facial surgery severing a facial nerve without graft or other form of dynamic facial nerve reconstruction within the last 5 years

Locations
United States
Texas
The University of Texas M. D. Anderson Cancer Center
RECRUITING
Houston
Contact Information
Primary
Z-Hye Lee, MD
zlee@mdanderson.org
713-563-4598
Time Frame
Start Date: 2025-01-13
Estimated Completion Date: 2028-08-01
Participants
Target number of participants: 40
Treatments
Experimental: Control
Participants will be identified and recruited during their visit to the Center of Reconstructive Surgery.
Experimental: Surgery
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov