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Effect of ipsilateral stellar ganglion block on postoperative delirium and analgesia in elderly patients undergoing thoracoscopic lobectomy

Effect of ipsilateral stellar ganglion block on postoperative delirium and analgesia in elderly patients undergoing thoracoscopic lobectomy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090154
Enrollment
Unknown
Registered
2024-09-25
Start date
2024-01-03
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Postoperative delirium

Interventions

Stellate ganglion block group (SGB group):Stellate ganglion block
blank control group (CON group):blank control

Sponsors

The First Hospital of Sanming; Fujian Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 65 years and older; 2. Patients requiring thoracoscopic lobectomy surgery; 3. American Society of Anesthesiologists (ASA) Class II or III patients; 4. Patients with no history of cognitive impairment or psychiatric disorders; 5. Patients who do not have allergies or overreactions to anesthetic drugs; 6. Patients who are not taking medications that affect nervous system function; 7. Voluntary trial, and written informed consent was obtained.

Exclusion criteria

Exclusion criteria: 1. History of thoracic surgery; 2. Change the surgical method during surgery; 3. bradycardia or arrhythmia; 4. Stroke or myocardial ischemia or infarction, severe arrhythmia, heart failure in the past 6 months;

Design outcomes

Primary

MeasureTime frame
Visual Analogue Score;3D-CAM;

Secondary

MeasureTime frame
The quality of recovery score (QoR)-15 questionnaire;Pulse oxygen saturation;mean arterial pressure;heart rate;restlessness;

Countries

China

Contacts

Public ContactWang Wentao

Department of Anesthesiology; The First Hospital of Sanming; Fujian Province

wwt1943@163.com+86 180 6017 1731

Outcome results

None listed

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