Ganglion Cyst Clinical Trials

Find Ganglion Cyst Clinical Trials Near You

Evaluating The Efficacy Of Combined Cognitive Processing Therapy and Stellate Ganglion Blocks for PTSD: A Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug, Behavioral
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

The purpose of this study is to understand if we can improve the treatment for posttraumatic stress disorder (PTSD). We are looking into whether the combination of Stellate Ganglion Block (SGB) treatment and Cognitive Processing Therapy (CPT) can reduce symptoms of PTSD. CPT is a trauma-focused talk therapy that can help identify and challenge unhelpful trauma-related beliefs about oneself, others, and the world. It is known to be a highly effective talk therapy for PTSD. SGB treatment is a procedure involving an injection of local anesthetic into a bundle of nerves located in the neck that is part of the sympathetic nervous system which controls our body's response to stressful situations and blocks pain. The proposed project will systematically test whether combining CPT with SGB produces greater PTSD symptom reductions and functional improvements in the short- and longer-term up to 6-months follow-up compared to CPT (+Placebo) or SGB (+Daily Monitoring) alone.

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

• Are 18 years or older

• Are fluent in English

• Have experienced a Criterion A traumatic event during their lifetime

• Have a PTSD diagnosis verified via the Clinician Administered PTSD Scale for DSM-5

• Have not previously received a Stellate Ganglion Block

• Have a smartphone that they can use for the entire duration of the study

• Are willing and able to receive 2 injections (SGB or placebo) 2 weeks apart at the Rush Pain Clinic

• Are willing and able to participate in daily Cognitive Processing Therapy or Daily Monitoring over the course of one week

• Are willing and able to complete self-report measures and clinician-rated assessments at multiple time points over the course of the study

Locations
United States
Illinois
Rush University Medical Center
RECRUITING
Chicago
Contact Information
Primary
Philip Held, PhD
philip_held@rush.edu
312-942-1423
Backup
Sarah Pridgen, MA
sarah_pridgen@rush.edu
312-563-0577
Time Frame
Start Date: 2026-04-01
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 270
Treatments
Active_comparator: Active Stellate Ganglion Block + Cognitive Processing Therapy
Participants in this arm will receive two active Stellate Ganglion Block Injections, two weeks apart. After receiving the first injection, participants will complete 10 sessions of Cognitive Processing Therapy over the course of one week.
Sham_comparator: Placebo Injection + Cognitive Processing Therapy
Participants in this arm will receive two placebo (saline) Injections, two weeks apart. After receiving the first injection, participants will complete 10 sessions of Cognitive Processing Therapy over the course of one week.
Placebo_comparator: Active Stellate Ganglion Block + Daily Symptom Monitoring
Participants in this arm will receive two active Stellate Ganglion Block Injections, two weeks apart. After receiving the first injection, participants will complete 5 sessions of daily symptom monitoring with a member of study staff over the course of one week.
Sponsors
Leads: Rush University Medical Center

This content was sourced from clinicaltrials.gov