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Effect of stellate ganglion block on posttraumatic stress disorder in patients undergoning emergency ocular trauma surgery: a randomized double-blind placebo-controlled trial

Effect of stellate ganglion block on posttraumatic stress disorder in patients undergoning emergency ocular trauma surgery: a randomized double-blind placebo-controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102717
Enrollment
Unknown
Registered
2025-05-19
Start date
2025-05-22
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posttraumatic stress disorder

Interventions

Stellate ganglion block group(SGB group):Stellate ganglion block with ropivacaine
Normal saline control group (NS group):normal saline control

Sponsors

the First Central Hospital of Baoding
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age 18 or older. 2.Acute unilateral or bilateral ocular trauma and scheduled for surgery under general anesthesia. 3.American Society of Anesthesiologists (ASA) physical status I-III E. 4.Provided informed consent, with approval from both patients and their families.

Exclusion criteria

Exclusion criteria: 1.A known allergy to ropivacaine. 2.Infection of the skin on the neck. 3.Combine severe neurological or mental disorders unable to undergo assessmtent. 4.Craniocerebral or spinal cord injury. 5.Shock decompensation. 6.Associated with multiple and complex injuries and requiring concurrent implementation of multiple surgical procedures. 7.Severe atrioventricular block or bradyarrhythmia with a baseline heart rate lower than 50 beats/min. 8.Severe visual, hearing, or speech impairments that prevent the completion of assessment.

Design outcomes

Primary

MeasureTime frame
Incidence of posttraumatic stress disorder;

Secondary

MeasureTime frame
The severity of PTSD;Intrusive re-experiencing;Avoidance;Negative alterations in cognition or mood;Hyperarousal and reactivity;Visual Analog Scale sleep scores;Numerical Rating Scale pain scores;Beck Anxiety Inventory score;Heart Rate Variablity ;Extubation time;Richmond Agitation Sedation Scale(RASS) score;Recovery time;Length of hospital stay ;

Countries

China

Contacts

Public ContactLei Zhu

the First Central Hospital of Baoding

leilei12192021@163.com+86 186 1778 9652

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026