The development of locating and puncture system for spinal minimally invasive surgery

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2000037374

Enrollment

Unknown

Registered

2020-08-28

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-10-19

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

Conditions

Lumbar disease

Interventions

experimental group:The application of the new locating and puncture system during spinal minimally invasive surgery

control group:Conventional minimally invasive surgery related instruments for lumbar minimally invasive surgery

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients who are above 18 years old with lumbar diseases. No gender limitation; 2. Patients who agree to participate this study and assignment is needed; 3. No severe basic disease. AST,ALT,BUN,Cr shouldn't be one time higher than normal level; 4. Patients with no HAV, HBV, AIDS or TB.

Exclusion criteria

Exclusion criteria: 1. Patients with general contraindications of surgery; 2. Patients with severe lumbar spinal stenosis, severe lumbar spondylolisthesis and severe scoliosis; 3. Patients with serious mental or mental illness; 4. Patients who are considered unsuitable to participate in this clinical study.

Design outcomes

Primary

Measure	Time frame
Puncture times;Surgery length;	—

Countries

China

Contacts

Public ContactShisheng He

Shanghai Tenth People's Hospital

hss7418@aliyun.com+86 13761645238

Outcome results

None listed

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