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Association of postoperative agitation with the risk factors of myeloid hypertension-like syndrome after percutaneous transforaminal endoscopic discectomy under general anesthesia: A retrospective cohort study

Association of postoperative agitation with the risk factors of myeloid hypertension-like syndrome after percutaneous transforaminal endoscopic discectomy under general anesthesia: A retrospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071283
Enrollment
Unknown
Registered
2023-05-10
Start date
2023-05-20
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Myeloid Hypertension-like Syndrome

Interventions

High-risk group :None
Control group :None

Sponsors

Shengjing Hospital Affiliated to China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. All patients were diagnosed with single-level lumbar disc herniation and underwent percutaneous endoscopic spinal discectomy under general anesthesia after conservative treatment failed; 2. The involved nerve roots of the lesion segments indicated by imaging examination were consistent with clinical manifestations and specialist physical examination; 3. Aged >= 18 years.

Exclusion criteria

Exclusion criteria: 1. Patients with serious underlying diseases cannot tolerate surgical general anesthesia; 2. A history of endoscopic discectomy or lumbar fusion; 3. There is lumbar stenosis, extreme lateral lumbar hernia or other spinal pathology; 4. There are active local or systemic infections, tumors and other diseases; 5. Coagulation dysfunction; 6. Combined with other nervous system diseases, such as cerebral hemorrhage, cerebral infarction, central nervous system infection, etc. 7. Patients with mental system diseases have recently taken mental system drugs, sedative sleeping pills, etc.

Design outcomes

Primary

MeasureTime frame
postoperative agitation;

Secondary

MeasureTime frame
therapeutic effect of postoperative agitation ;

Countries

China

Contacts

Public ContactXu Ying

Shengjing Hospital Affiliated to China Medical University

xuy5@sj-hospital.org+86 189 4025 4252

Outcome results

None listed

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