Skip to content

Effect of opioid-free general anesthesia on perinatal pain and neonatal outcomes during elective caesarean section A randomized controlled trial

Effect of opioid general anesthesia on perinatal pain and neonatal outcomes during elective caesarean section A randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072161
Enrollment
Unknown
Registered
2023-06-05
Start date
2023-06-05
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

elective caserean section

Interventions

opioid-free group:Intravenous infusion of esketamine 0.15mg / kg and lidocaine 1.5mg / kg
control group:Intravenous infusion of sufentanyl at 0.3mg / kg, and the same appearance of normal saline

Sponsors

Yichang Central People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1) Age: 18-35 years old; 2) ASA grade; 3) For elective cesarean section; 4) Agree to participate in the questionnaire survey.

Exclusion criteria

Exclusion criteria: 1) Pregnant women with other diseases and not well controlled, such as hypertension, diabetes, chronic pain, epilepsy, asthma, renal function impairment (BUN and or Cr> 2 times normal value), liver function impairment (ALT and OT AST> 1.5 times normal value), etc.; 2) Combined with special obstetric conditions: placental abruption, placenta previa with bleeding, fetal abnormalities, twin or multiple pregnancy; 3) Pregnant women who need an emergency caesarean section due to special circumstances, such as fever with acute infection, trauma, premature rupture of membranes with fetal distress, etc.; 4) Pregnant women with allergies to any anesthetic ingredients; 5) Reuse, disagree, failure to understand the scale survey or anesthesia protocol; 6) Patients with other circumstances considered not suitable for inclusion;

Design outcomes

Primary

MeasureTime frame
time weighted average of postoperative pain scores;apgar scores;

Secondary

MeasureTime frame
Blood and gas analysis of umbilical artery and vein;Intraoperative hemodynamic parameters;

Countries

China

Contacts

Public ContactYuan Gong

School of Basic Medicine of Three Gorges University, First Clinical Medical College of Three Gorges University, Yichang Central People's Hospital

gy-yc@163.com+86 139 8674 6821

Outcome results

None listed

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