Comparison of epidural anesthesia with different epidural puncture point and catheter orientation

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR-IIR-16008453

Enrollment

Unknown

Registered

2016-05-09

Start date

2016-05-07

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

Surgical disease

Interventions

four:Different catheter orientation

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) elective lower abdominal surgery or lower limb surgery; 2) to sign the informed consent form; 3) ASAI~II class; 4) aged 60 ~ 4 years old; 5) the gender is not limited.

Exclusion criteria

Exclusion criteria: 1 refusal to sign the informed consent form; 2. the existence of the epidural anesthesia; 3. the history of chronic pain; 4. the history of mental illness and mental disease; 5. a clear diagnosis of cardiac or vascular disease; 6. the history of peptic ulcer bleeding; 7. renal insufficiency (serum creatinine >133mmmol/L); 8. liver dysfunction (AST or ALT or both >40 and U/L); 9. unable to communicate or exchange; 10. to participate in other clinical trials within 10 months.

Design outcomes

Primary

Measure	Time frame
lumbago;	—

Countries

China

Contacts

Public ContactZhong Qiaosheng

Taizhou Municipal Hospital

qszhong2013@163.com+86 18957608256

Outcome results

None listed

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