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Spinal anaesthesia for lower limb surgery: dose-response study of ropivacaine

Spinal anaesthesia for lower limb surgery: dose-response study of ropivacaine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-06000681
Enrollment
Unknown
Registered
2006-03-21
Start date
2005-06-01
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

Lower limb surgery

Interventions

Two groups:Spinal anaesthesia using ropivacaine in 2~3 hours versus Varying doses of intrathecal ropivacaine

Sponsors

Department of Anaesthesiology and Operating Theatre Services, Kwong Wah Hospital, Kowloon, Hong Kong
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: ASA 1-3 patients, >18years, weight 45-85 kg, height >150 cm having spinal anaesthesia for lower limb surgery.

Exclusion criteria

Exclusion criteria: hypersensitivity to local anaesthetics, contraindications to spinal anaesthesia, inability to understand Chinese or English.

Design outcomes

Primary

MeasureTime frame
Effectiveness of spinal anaesthesia;—

Countries

China

Contacts

Public ContactDr Ying Y LEE
yylee@ha.org.hk+8523 26322735

Outcome results

None listed

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