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Use of Subanesthetic Esketamine Plus Propofol for Painless Induced Abortion Procedures

Use of Subanesthetic Esketamine Plus Propofol for Painless Induced Abortion Procedures

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122375
Enrollment
Unknown
Registered
2026-04-13
Start date
2025-06-24
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

None

Interventions

Sponsors

Meizhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1.People aged 18 to 45; 2.American Society of Anesthesiologists (ASA) physical status classification: Class I - II. 3.No allergy to the drugs under study. 4.No administration of sedatives or antidepressants before the surgery. 5.Meeting the requirements for gynecological induced abortion surgery, with a gestational age within 12 weeks. 6.The patient voluntarily signed the informed consent form;

Exclusion criteria

Exclusion criteria: 1.Those with recent upper respiratory tract infections; 2.Has a history of past psychiatric disorders; 3.Patients with Obstructive Sleep Apnea Hypopnea Syndrome (OSAHS) and obese patients (BMI > 28 kg/m^2); 4.Those with severe hepatic and renal insufficiency; 5.Those with severe nervous system and cardiovascular system diseases; 6.Those with hyperthyroidism.

Design outcomes

Primary

MeasureTime frame
Self-Rating Anxiety Scale (SAS) Score;Psychiatric Symptoms;Self-Rating Depression Scale (SDS) Score;Hypotension;Postoperative Pain(Visual Analogue Scale (VAS) for Pain);Respiratory Depression;

Secondary

MeasureTime frame
Nausea and Vomiting;Injection Pain;Dizziness;

Countries

China

Contacts

Public ContactLin Jian

Meizhou People's Hospital

wolfly888@163.com+86 137 5055 5121

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026