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A prospective clinical study investigating the optimal concentration of low-concentration spinal anesthesia for endoscopic lumbar nucleus pulposus extraction

A prospective clinical study investigating the optimal concentration of low-concentration spinal anesthesia for endoscopic lumbar nucleus pulposus extraction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082845
Enrollment
Unknown
Registered
2024-04-09
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

lumbar disc herniation

Interventions

The sequential method for designing a biased coin test group with a single arm.:Sequential design for titration of lumbar anesthesia concentration.
Optimal concentration group (O group):The lumbar anesthesia was administered based on the optimal concentration of ropivacaine determined by the initial test results
Conventional group (C group):The lumbar anesthesia was conducted using a standard concentration of ropivacaine(0.5%).

Sponsors

Ningbo No.6 Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade I-II; 2. Age range of 18-70 years; 3. BMI between 18 and 35 kg/m2; 4. Patients opting for PELD and providing voluntary informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with contraindications to excessive local anesthesia and epidural anesthesia; 2. Patients with severe systemic diseases, as well as those with intellectual disabilities or inability to communicate. 3. Other clinical trials are already in progress.

Design outcomes

Primary

MeasureTime frame
VAS pain score;

Secondary

MeasureTime frame
ODI score;The monitoring of vital signs during surgery;

Countries

China

Contacts

Public ContactLong Zhang

Ningbo No.6 Hospital

nblylmz@126.com+86 136 8573 7816

Outcome results

None listed

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