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Transient Neurologic Symptoms (TNS) following Spinal Anesthesia with Bupivacaine and Ropivacaine

Retrospective study on Transient Neurologic Symptoms following Spinal Anesthesia with Bupivacaine and Ropivacaine

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023380
Enrollment
Unknown
Registered
2019-05-25
Start date
2019-05-24
Completion date
Unknown
Last updated
2019-05-27

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

Conditions

Patients undergoing spinal anesthesia

Interventions

bupivacaine group:bupivacaine

Sponsors

The First People’s Hospital of Shuangliu District, Chengdu
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) patients undergoing elective spinal anaesthesia for 1 ~ 2 h; 2) ASA classification: level I~ II.

Exclusion criteria

Exclusion criteria: 1) patients using analgesic pump; 2) postoperative patients with nerve block; 3) postoperative patients taking analgesics; 4) acute infection occurred after surgery; 5) patients with incomplete postoperative case data; 6) history of serious cardiovascular diseases (e.g., coronary heart disease or congenital heart disease, grade 3 or above cardiac function); 7) history of alcohol and drug use; 8) mental disorders, unable to communicate normally;

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Demographic data;

Countries

China

Contacts

Public ContactHu Yue

The First People’s Hospital of Shuangliu District, Chengdu

18227648792@163.com+86 18227648792

Outcome results

None listed

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