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Effect of Ultrasound-Guided Superior Cervical Ganglion Block on Postoperative Sleep Disturbance and Pain in Patients Undergoing Thoracoscopic Surgery

Effect of Ultrasound-Guided Superior Cervical Ganglion Block on Postoperative Sleep Disturbance and Pain in Patients Undergoing Thoracoscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128280
Enrollment
Unknown
Registered
2026-07-17
Start date
2026-07-17
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Postoperative sleep disturbance and postoperative pain after video-assisted thoracoscopic surgery

Interventions

Control Group:Routine Perioperative Management (Sham Block)
Ultrasound-Guided Superior Cervical Ganglion Block Group (SCGB Group):Ultrasound-Guided Superior Cervical Ganglion Block

Sponsors

Taizhou Central Hospital(Taizhou University Hospital )
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-75 years, regardless of gender; 2.American Society of Anesthesiologists (ASA) physical status classification I-III; 3.Patients with pulmonary space-occupying lesions requiring elective video-assisted thoracoscopic surgery (VATS) under general anesthesia; 4.Voluntary participation in the study and signed informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients unable to cooperate, with impaired consciousness, or unable to maintain body position. 2.Infection at the puncture site. 3.Coagulation dysfunction. 4.Allergy to local anesthetics. 5.Severe deformity or tumor invasion in the skull base, cervical spine, or upper neck anatomy. 6.Uncontrolled severe hypertension or increased intracranial pressure. 7.Glaucoma (especially angle-closure glaucoma). 8.Recent cerebrovascular events or severe cerebral hypoperfusion. 9.Preoperative severe sleep disturbance (Athens Insomnia Scale score =16). 10.Patients requiring conversion to thoracotomy during surgery. 11.Intraoperative blood loss > 800ml or operation time > 4 hours.

Design outcomes

Primary

MeasureTime frame
Postoperative Sleep Disturbance;

Secondary

MeasureTime frame
Postoperative Numerical Rating Scale (NRS) score;

Countries

China

Contacts

Public ContactYan feng

Taizhou Central Hospital(Taizhou University Hospital )

fengy8221@tzzxyy.com+86 576 8852 6144

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026