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Effect of Esketamine on Postoperative Anxiety in Patients Undergoing Dilatation and Curettage after Missed Abortion during in Vitro Fertilization Treatment: A Prospective Cohort Observational Study

Effect of Esketamine on Postoperative Anxiety in Patients Undergoing Dilatation and Curettage after Missed Abortion during in Vitro Fertilization Treatment: A Prospective Cohort Observational Study

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080537
Enrollment
Unknown
Registered
2024-01-31
Start date
2024-02-04
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Effect of Esketamine on Postoperative Anxiety in Patients Undergoing Dilatation and Curettage after Missed Abortion during in Vitro Fertilization Treatment

Interventions

Group C (saline group, 0.1ug/kg sufentanil + propofol 1mg/kg):None
Group E1 (sufentanil + 0.2mg/kg esketamine + propofol):None
Group E2 ( sufentanil + 0.35mg/kg esketamine +propofol):None
Group E3 (sufentanil + 0.5mg/kg esketamine +propofol):None

Sponsors

Sichuan Jinxin Xi'nan Women's and Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
23 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1) Diagnosed with infertility and undergoing IVF treatment at our hospital; 2) Age 23-45; 3) Comply with the diagnostic standards for induced abortion; 4)ASA I-II; 5) elective surgery of painless curettage; 6) Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Patients with preoperative psychiatric dysfunction and those taking psychotropic medications preoperatively; 2) Allergy to the drugs involved in this study; 3) Severe cardiac, pulmonary, hepatic and renal organ insufficiency; 4) History of upper respiratory tract infection in the last 2 weeks; 5) Poorly controlled or untreated hypertension (resting systolic/diastolic blood pressure over 180/100 mmHg); 6) Patients with hyperthyroidism and those at risk of increased intracranial pressure; 7) History of psychotropic drugs, opioids, and alcohol dependence; 8) Taking benzodiazepines or opioids during the last 3 months; 9) Participation in clinical trials of other drugs within the last 3 months; 10) Communication barriers; 11) Change in anaesthesia; 12) Patients and their families refused to participate in this study.

Design outcomes

Primary

MeasureTime frame
The incidence of anxiety ;Pregnancy outcomes;

Secondary

MeasureTime frame
The incidence of moderate to severe anxiety;The incidence anxiety;SAS score;SDS score;The incidence of depression;Incidence of intraoperative body movements;Incidence of respiratory depression;Intraoperative circulatory fluctuations;Postoperative NRS scores;Postoperative remedial analgesic dose;Postoperative adverse events;Length of stay in PACU;Wake-up time;Intraoperative propofol dose;

Countries

China

Contacts

Public ContactNI JUAN LI

Sichuan Jinxin Xi'nan Women's and Children's Hospital

22392783@qq.com+86 138 8042 6626

Outcome results

None listed

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