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Application of Fine Needle isobaric Spinal Anesthesia in Lower limb Orthopaedic surgery in patients with abnormal Spinal structure

Application of Fine Needle isobaric Spinal Anesthesia in Lower limb Orthopaedic surgery in patients with abnormal Spinal structure

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300073435
Enrollment
Unknown
Registered
2023-07-11
Start date
2023-01-20
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

Structural abnormality of spine

Interventions

Normal spinal structure group:None
Abnormal spinal structure group:None

Sponsors

Department of Anesthesiology, people's Hospital of Ningxia Hui Autonomous region
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients in the People's Hospital of Ningxia Hui Autonomous Region who need lower extremity orthopedic surgery under lumbar anesthesia from February 2023 to September 2023, aged 18-100 years old, ASA: grade I-III, who are aware of the content and significance of this study, and sign the informed consent

Exclusion criteria

Exclusion criteria: Previous mental disorders, central nervous system diseases, myasthenia gravis, autoimmune diseases; blood coagulation disorders, puncture site infection or systemic infection, nervous system complications caused by spinal surgery or spinal structural abnormalities; those who were unable to communicate before operation due to coma, severe dementia, language disorder, end-stage diseases, and spinal injury within 72 hours. Critical condition (preoperative ASA grade = IV); severe renal function damage (need renal replacement therapy); severe liver function damage (Child-Pugh grade C); severe cardiac insufficiency (NYHA = grade ?); other conditions that the attending doctor or researcher considered unsuitable to participate in this study; those who refused to participate in this study and their families.

Design outcomes

Primary

MeasureTime frame
Neurological complications associated with intraspinal anesthesia (within one month);

Secondary

MeasureTime frame
Total duration of intraspinal anesthesia sensory block;Low back pain;Intraoperative hemodynamic changes;Number of puncture;Puncture space selection;Whether there was any abnormal sensation in the lower extremities during puncture;Highest anesthesia plane;Success rate of intraspinal anesthesia block;Score of motor block degree before operation;Score of sensory block before operation;Pain score during peeling (NRS score);Whether adverse reactions occurred during the operation;Adverse reactions to postoperative intraspinal anesthesia (within 3 days);Total duration of intraspinal anesthesia motor block;Total puncture time;Time to inject lumbar anesthesia drugs;Onset time of sensory block;Onset time of motor block;

Countries

China

Contacts

Public ContactYe Qingshan

Department of Anesthesiology, people's Hospital of Ningxia Hui Autonomous region

yeqingshan@hotmail.com+86 173 9505 5188

Outcome results

None listed

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