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The Effects of Stellate Ganglion Block on Sleep in U.S. Active Duty Service Members and Veterans Receiving Prolonged Exposure Therapy for Posttraumatic Stress Disorder (PTSD)

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

Participants in this study will have already been enrolled in another research study: Combining Stellate Ganglion Block with Prolonged Exposure for PTSD, NCT05889741. The investigators are using a Sleep Profiler, EEG headband to monitor a participants brainwaves while they sleep to see what effects the Stellate Ganglion Block injection has on their sleep. Participants will wear the headband for 3 nights before the injection and then 3 nights after the injection. Participants will also complete self-report questionnaires regarding their sleep prior to the injection and following the injection. Approximately 40 participants will be included in this study. This study is a nested observational study whereby participants in the parent study who elect to participate will have their sleep assessed using the EEG headband device and self-reported sleep measures performed.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Ability to provide informed consent and follow study-related instructions.

• Be randomized into the study titled Combining Stellate Ganglion Block with Prolonged Exposure for PTSD: A Randomized Clinical Trial. NCT05889741

• Indicates willingness to wear the Sleep Profiler sleep monitor and to complete self-report assessments.

Locations
United States
Texas
Carl R. Darnall Army Medical Center at Fort Hood
RECRUITING
Killeen
University of Texas Health Science Center at San Antonio
RECRUITING
San Antonio
Contact Information
Primary
Kristi E Pruiksma, PhD, DBSM
pruiksma@uthscsa.edu
(210) 562-6700
Time Frame
Start Date: 2026-06-15
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 40
Treatments
Massed Prolonged Exposure (PE) with SGB group
Participants will wear the EEG headband monitoring device (Sleep Profiler)for 3 nights as a baseline prior to SGB injection administered as part of enrollment in original study from which they were recruited. After the SGB injection, participants will wear the headband monitoring device for 3 nights.
Massed PE Exposure with Sham SGB
Participants will wear the EEG headband monitoring device (Sleep Profiler) for 3 nights as a baseline prior to the sham SGB injection administered as part of enrollment in original study from which they were recruited. Participants will wear the EEG headband monitoring device for 3 nights following the sham SGB injection.
Sponsors
Collaborators: Trauma Research and Combat Casualty Care Collaborative (TRC4)
Leads: The University of Texas Health Science Center at San Antonio

This content was sourced from clinicaltrials.gov