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Effect of esketamine combined with Ropivacaine on epidural labor analgesia

Effect of esketamine combined with Ropivacaine on epidural labor analgesia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109086
Enrollment
Unknown
Registered
2025-09-11
Start date
2024-06-12
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Painless labor

Interventions

Esketamine group:Esketamine 1mg/ml was added to the delivery analgesic pump, respectively
Sufentanil group:and Sufentanil 0.3ug/ml was added to the delivery analgesic pump, respectively

Sponsors

Chinese People's Liberation Army Northern Theater Command General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-40 years old, ASA grade I to II, BMI BMI=37 weeks, single fetus, cephalic primipara/menpara, the mother and her family agreed to labor analgesia and signed informed consent; 3. no contraindications to intraspinal anesthesia; 4. The obstetrician and midwife assessed regular uterine contractions and met the conditions for vaginal birth.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to the active ingredient esketamine or local anesthetics; 2. The maternal cannot cooperate with the spinal canal puncture or can not cooperate with the scores, the maternal does not agree and refuses to sign the informed consent; 3. those who withdrew from the experiment and those whose results were suspicious; 4. High blood pressure or preeclampsia during pregnancy; 5. Patients who have or have had a history of serious mental disorders; 6. There are contraindications for intraspinal block, such as coagulation dysfunction, puncture site infection or injury, uncorrected maternal hypovolemia or hypotension, increased intracranial pressure, severe spinal deformity, etc.;

Design outcomes

Primary

MeasureTime frame
Pain score 30min after the first dose;Pain score 24h after administration;

Secondary

MeasureTime frame
Sleep scores ; Depression scores;Systolic blood pressure, diastolic blood pressure, heart rate, blood oxygen saturation, body temperature;First time of getting out of bed, first time of exhalation, first time of defecation, length of hospital stay;

Countries

China

Contacts

Public ContactLin Li

Chinese People's Liberation Army Northern Theater Command General Hospital

Lilin100@qq.com+86 159 0988 3195

Outcome results

None listed

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