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Enhancing the Effect of Stellate Ganglion Block in the Treatment of Posttraumatic Stress Disorder: A Double-blind Randomized Controlled Trial of Bupivacaine vs Bupivacaine + Ketamine

3. november 2026 oppdatert av: Rebecca Gomez, MD, The Royal's Institute of Mental Health Research

The goal of this clinical trial is to learn whether stellate ganglion block (SGB), with or without ketamine, can reduce symptoms of post-traumatic stress disorder (PTSD) in adults receiving care through the Operational Stress Injury (OSI) Clinic and military community partners. The main questions it aims to answer are:

Does adding ketamine to the standard SGB anesthetic (bupivacaine) improve treatment effectiveness compared with bupivacaine alone?

Does SGB reduce PTSD symptom severity compared with no injection (control group)?

Researchers will compare participants receiving SGB with bupivacaine, SGB with bupivacaine plus ketamine, and no injection (control) to determine whether SGB reduces PTSD symptoms and whether ketamine enhances the effects of the procedure.

Participants will:

Be randomly assigned to receive SGB with bupivacaine, SGB with bupivacaine plus ketamine, or no injection during the randomized controlled trial portion of the study.

Complete questionnaires and clinical interviews assessing PTSD symptoms, anxiety, depression, functioning, and quality of life.

Participate in follow-up interviews to discuss their experiences with the treatment.

Invite a family member or support person to complete a questionnaire about observed changes in symptoms and functioning.

Have the option to receive a standard SGB procedure during the study extension phase, if eligible.

This study will enroll approximately 126 participants and aims to improve understanding of how SGB works for PTSD and whether ketamine can enhance its therapeutic effects.

Studieoversikt

Detaljert beskrivelse

The most common treatment for Post-traumatic Stress Disorder (PTSD) is trauma-focused therapy and/or prescription of medication(s). However, these treatments may not directly reduce symptoms associated with PTSD, making it difficult for patients to be treated for this condition and recover.

Stellate ganglion block (SGB) is a medical procedure that involves injection of a local anesthetic (a medication that causes reduced sensation/feeling in a given area) around the stellate ganglion, which is a collection of nerves near the base of the neck. This procedure causes a short-lived, temporary shutdown of nerve signals (up to 5-7 hours) and is commonly performed in Canada for certain pain and medical conditions. In the last decade, several studies, including those involving members of military groups, have shown that SGB can result in a rapid and sustained drop in symptoms related to PTSD such as overwhelming anxiety, increased irritability, heightened alertness, and exaggerated startle. Considering these results and the known safety of this procedure (as demonstrated by previous research and use in other illnesses), SGB has been increasingly used to treat PTSD among veterans in the United States but has not yet been thoroughly evaluated in Canada. More research is thereby needed to use SGB as a method of PTSD treatment in Canada, and to better understand how it works to reduce symptoms associated with this condition.

The use of the SGB procedure for PTSD has not yet been approved by Health Canada for the general population.

WHY IS THIS STUDY BEING DONE? The purpose of this study is to better understand how SGB works in helping reduce symptoms associated with PTSD, and to understand if infusing bupivacaine (the standard local anesthetic used for SGB) with ketamine increases the effectiveness of the procedure. Combining ketamine with local anaesthetics such as lidocaine or bupivacaine is a specialized approach used in interventional pain management. Research has shown that this combination works safely in providing powerful relief for severe treatment resistant chronic conditions. However, combining ketamine in the context of an SGB injection, or as a supporting treatment for PTSD symptoms, has yet to be studied.

To do this, the study will have two Parts. The first Part is the Randomized Controlled Trial (RCT), and the second Part is the study extension. In Part I, participants will be randomized into groups where they will either receive one SGB injection of bupivacaine alone, one injection of bupivacaine combined with ketamine, or no injection. We will also be collecting additional information through the use of pupillometry (a non-invasive technique that measures the size and reactivity of your pupil) to monitor the effectiveness of each individual procedure. Additionally, during this project we hope to obtain feedback from both the participant and their family/support network about their experience and satisfaction with the SGB procedure and its effects. This will help us understand for whom SGB works best and will provide us with information and experience for introducing SGB into programs within The Royal. A series of questionnaires will also be asked to understand more about each participant.

In Part II, all participants who meet eligibility criteria, including those who received no injection during Part I, will have the option to finish and exit the study, or continue and receive one standard SGB injection (bupivacaine) during the extension. This means those who received an injection during the RCT will have the option for a second injection, and those who were randomized to the Control Group will have the option to receive one injection.

Studietype

Intervensjonell

Registrering (Antatt)

126

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studer Kontakt Backup

  • Navn: Krysta Boutin-Miller, Research Coordinator
  • Telefonnummer: 6137226521
  • E-post: kboutin@theroyal.ca

Studiesteder

    • Ontario
      • Ottawa, Ontario, Canada, K1Z 7K4
        • The Royal
        • Ta kontakt med:
          • Tammy Beaudoin, Director, Clinical Research
          • Telefonnummer: 6214 613-722-6521
          • E-post: tbeaudoin@theroyal.ca

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 69 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. DSM-5 diagnosis of PTSD of at least moderate severity confirmed by PCL-5 score ≥33 or CAPS-5 score ≥26 at screening visit
  2. Age 18-69 years
  3. Under care of a mental health clinician
  4. Has not benefited from pharmacological and/or psychological evidence-based treatments for PTSD

Exclusion Criteria:

  1. Assessed with high risk for suicide in the last 30 days
  2. Active mania/ hypomania or psychosis within the last 30 days
  3. Moderate to severe substance use within the last 30 days
  4. In process of disability assessment or legal action
  5. Current participation in another treatment study for PTSD
  6. Pregnancy or breastfeeding confirmed by urine test
  7. Current anticoagulant use (eligible if can be held before the procedure)
  8. History of bleeding disorder
  9. Infection, mass or anatomic abnormalities at target injection site
  10. Myocardial infarction within 6 months of procedure
  11. Pathologic bradycardia or irregularities of heart rate or rhythm;
  12. Symptomatic hypotension
  13. Phrenic or laryngeal nerve palsy
  14. History of glaucoma
  15. Uncontrolled seizure disorder
  16. History of allergy to local anesthetics
  17. History of allergy to general anesthetics
  18. Severe chronic obstructive pulmonary disease (COPD)
  19. Current or reoccurring Pneumothorax
  20. Contralateral pneumonectomy or non-functional lung
  21. Active systemic infection
  22. Bilateral procedure is always contraindicated due to risk of laryngeal/phrenic nerve dysfunction
  23. Participant refusal/inability to tolerate procedure/positioning
  24. End stage renal disease
  25. Known allergy to Ketamine
  26. Unable to hold stimulant or benzodiazepine medication prior to SGB procedure

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Group 1: One SGB injection with standard local anesthetic, bupivacaine

One dose of 6mL 0.5% bupivacaine combined with 2ml normal saline. The dose and medication provided to Group 1 is in line with current research practice for SGB which suggests a dosage between 6mL and 9 mL of local anaesthetic. Saline is included in the injection to match the volume of the injection for Group 2 without adding additional medical properties to the solution.

6 mL of 0.5% preservative-free bupivacaine plus 2 mL normal saline

Eksperimentell: Group 2: One SGB injection combining standard local anesthetic, bupivacaine, with Ketamine

The bupivacaine dose administered to Group 2 is identical to that administered to Group 1, with the addition of 20 mg ketamine (2 mL of a 10 mg/mL solution). A fixed ketamine dose of 20 mg was selected to approximate a low-dose (subanesthetic) exposure of 0.3 mg/kg in a 70 kg adult (21 mg), while allowing standardized dosing across participants. This dose was chosen to remain within a range commonly used in clinical research investigating the analgesic and neuropsychiatric effects of ketamine. This is the accepted standard and widely used dose in clinical practice.

6 mL of 0.5% preservative-free bupivacaine plus 2 mL ketamine (10 mg/mL)

Andre navn:
  • Group 2: One SGB injection combining standard local anesthetic, bupivacaine, with Ketamine
Ingen inngripen: Group 3: Treatment as usual

Participants selected to this group will not receive any intervention and continue with their treatments as usual.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change of the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) total symptom severity score
Tidsramme: From baseline to +4 weeks

The mean difference in the change of the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) total symptom severity score, specifically evaluated by comparing the Bupivacaine + Ketamine group to the Bupivacaine alone group.

From baseline to +4 weeks
Change of the Clinician-Administered PTSD Scale for DSM-5 (CAPS-5) total symptom severity score
Tidsramme: From baseline to +4 weeks

The mean difference in the change of the CAPS-5 total symptom severity score , specifically evaluated by comparing the Bupivacaine + Ketamine group to the Control group.

From baseline to +4 weeks

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
The mean change in PTSD Check List-5 (PCL-5) scores
Tidsramme: From baseline to +4 weeks

The mean change in PCL-5 scores between the Bupivacaine + Ketamine group and the Bupivacaine alone group.

From baseline to +4 weeks
The mean change in PCL-5 scores
Tidsramme: From baseline to +4 weeks

The mean change in PCL-5 scores between the Bupivacaine + Ketamine group versus the Control group.

From baseline to +4 weeks
Proportion of patients achieving reliable change (at least 14-point reduction) in the total score on Outcome Questionnaire 45 (OQ45)
Tidsramme: from baseline to +4, +8 and +12 weeks.

Proportion of patients achieving reliable change (at least 14-point reduction) in the total score on OQ45.2 reflecting improvement in symptom burden and functioning

from baseline to +4, +8 and +12 weeks.
Changes in participant's symptomatology and overall functioning from the perspective of the participant's family and support network measured by the FAST-Q
Tidsramme: From baseline to +4 and +12 weeks

Changes in participant's symptomatology and overall functioning from the perspective of the participant's family and support network measured by the FAST-Q

From baseline to +4 and +12 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Rebecca J Gomez, MD, Research Institute (IMHR) at The Royal, Ottawa campus

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. februar 2027

Primær fullføring (Antatt)

1. februar 2029

Studiet fullført (Antatt)

1. februar 2029

Datoer for studieregistrering

Først innsendt

3. november 2026

Først innsendt som oppfylte QC-kriteriene

3. november 2026

Først lagt ut (Faktiske)

9. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

9. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

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UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

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