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Comparison of different evaluation methods of epidural anesthesia block level during cesarean section

Comparison of different evaluation methods of epidural anesthesia block level during cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200055324
Enrollment
Unknown
Registered
2022-01-07
Start date
2022-01-07
Completion date
Unknown
Last updated
2023-01-23

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

Conditions

None listed

Interventions

Acupuncture test group:prick assessment block level
Cold sensation test group:cold sensory assessment block level
Touch test group:touch sensory assessment block level

Sponsors

Shaoxing Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Full-term women who plan to perform elective cesarean section under epidural anesthesia, without spinal deformity and contraindications to epidural puncture; 2. ASA score II and III; 3. Those with normal intelligence, language and hearing, and those with no barrier to skin; 4. The weight is 50-110Kg, the height is 150cm-175cm, and the BMI is less than 40Kg/m^2; 5. No preoperative hypertension, hypotension, bradycardia, nausea and vomiting, chills, dyspnea, etc., and no history of local anesthetic allergy.

Exclusion criteria

Exclusion criteria: 1. Epidural puncture and block failure; 2. Major intraoperative bleeding (defined as blood loss >= 1000ml); 3. Those who use other uterine contraction drugs other than conventional oxytocin during the operation, and those who perform hysterectomy during the operation.

Design outcomes

Primary

MeasureTime frame
Incidence of compound adverse reactions;

Secondary

MeasureTime frame
Comfort score of parturient;Dosage of intravenous analgesics;Satisfaction of surgeon;Operation waiting time;

Countries

China

Contacts

Public ContactZhou Liwang

Shaoxing Maternal and Child Health Hospital

15925886571@126.com+86 15925886571

Outcome results

None listed

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