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Association between plain ropivacaine dose and maternal hypotension in women undergoing cesarean delivery under spinal anesthesia

Association between plain ropivacaine dose and maternal hypotension in women undergoing cesarean delivery under spinal anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300071440
Enrollment
Unknown
Registered
2023-05-16
Start date
2023-05-16
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

the occurrence of spinal-induced hypotension

Interventions

Case series:None

Sponsors

The first hospital of Fuyang Hangzhou
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients who underwent cesarean delivery with single-shot spinal or combined spinal-epidural (CSE) anesthesia using plain ropivacaine in The First Hospital of Fuyang,Hangzhou among 2018 to 2022.

Exclusion criteria

Exclusion criteria: General and epidural anesthesia for cesarean delivery , Women who received CSE and had epidural top-up .

Design outcomes

Primary

MeasureTime frame
the occurrence of spinal-induced hypotension;—

Secondary

MeasureTime frame
vasopressor use;—

Countries

China

Contacts

Public ContactMin Li

The first hospital of Fuyang Hangzhou

15857134355@163.com+86 158 5713 4355

Outcome results

None listed

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