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Effect of preoperative anxiety on cipofol ED90 in patients undergoing painless oocyte retrieval combined with remifentanil

Effect of preoperative anxiety on cipofol ED90 in patients undergoing painless oocyte retrieval combined with remifentanil

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092099
Enrollment
Unknown
Registered
2024-11-10
Start date
2024-11-11
Completion date
Unknown
Last updated
2024-11-18

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

Conditions

Preoperative anxious infertile women

Interventions

Low anxiety group (Group L):None
medium and high anxiety group (group H):None

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1) Painless egg retrieval under intravenous anesthesia/sedation 2) ASA classification I~II 3) Age 18-45 years old 4) 18 ~ 25 kg/m2 5) Voluntarily participate in the study and sign the informed consent

Exclusion criteria

Exclusion criteria: 1) Anyone who meets any of the following criteria is not eligible for inclusion: 1) Serious dysfunction of nervous and circulatory system 2) long-term use of anti-anxiety drugs, antidepressants, analgesics and sedatives 3) A history of alcohol or drug abuse 4) Can not complete the anxiety scale 5) The high position of the ovary requires external assistance through the abdominal wall 6) Allergic history of cyclopofol or other fat emulsions

Design outcomes

Primary

MeasureTime frame
Depth of sedation;Intraoperative hemodynamic changes;

Secondary

MeasureTime frame
Recovery time;Cyclopofol dosage;

Countries

chinese

Contacts

Public ContactNa Xing

The First Affiliated Hospital of Zhengzhou University

16427485@qq.com+86 139 4909 5172

Outcome results

None listed

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