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Comparison of 0.75% ropivacaine versus chloroprocaine for epidural extension anesthesia in urgent cesarean delivery

Comparison of 0.75% ropivacaine versus chloroprocaine for epidural extension anesthesia in urgent cesarean delivery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200065201
Enrollment
Unknown
Registered
2022-10-31
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

the onset time of anaesthesia

Interventions

Ropivacaine group: 20 ml ropivacaine was given epidurally
Chloroprocaine group:20ml chloroprocaine was given epidurally

Sponsors

Hangzhou Women's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. over 18 years old; 2. ASA physical status 1 or 2; 3. gestation >= 36 weeks; 4. singleton pregnancy; 5. effective labor analgesia (defined as requiring two or fewer intrapartum epidural supplements with 0.2% ropivacaine) ; 6. Patients undergoing urgent cesarean section

Exclusion criteria

Exclusion criteria: 1.epidural intrapartum supplementation less than two hours from caesarean section or intramuscular pethidine injection within four hours 2.emergency cesarean section 3.severe fetal anomalies 4.pre-eclampsia eclampsia, antepartum haemorrhage or any form of cardiac disease 5.height 115 kg 6.allergy to any study medications

Design outcomes

Primary

MeasureTime frame
the onset time of anaesthesia;

Secondary

MeasureTime frame
Age, height, weight, gestational age,Indication for operative delivery, Abdominal girth;Preoperative information:Duration of analgesia ;Epidural loading dose ;Total dose ;Time since last intrapartum supplementation ;Surgical procedure; Pre-existing block (cold) ;Pre-existing block (touch); Bromage score ;Preoperative IV fluid.;Intraoperative information:Time from anesthesia to operation Intraoperative ;VAS score ;patients requiring IV Esketamine during surgery ;VAS score ;reported during IV Esketamine supplementation; Side effects; Intraoperative IV fluids ;Phenylephrine dose; APGAR score at 1,5 mins ;Surgery time ;bromage score for block to recede two&;HR?Blood pressure;

Countries

China

Contacts

Public ContactMen Xin

Hangzhou Women's Hospital (Hangzhou First People's Hospital Qianjiang New City Campus, The Affiliated Women's Hospital of Hangzhou Normal University)

rourouzong@163.com+86 15067196256

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026