Geneva, April 28 -- International Clinical Trials Registry received information related to the study (ChiCTR2600122375) titled 'Use of Subanesthetic Esketamine Plus Propofol for Painless Induced Abortion Procedures' on April 13.
Study Type: Interventional study
Study Design:
Parallel
Primary Sponsor: Meizhou People's Hospital
Condition:
None
Intervention:
Sufentanil combined with Propofol group:Sufentanil combined with Propofol
Recruitment Status: Recruiting
Phase: N/A
Date of First Enrollment: 2025-06-24
Target Sample Size: Sufentanil combined with Propofol group:40;Esketamine combined with Propofol group:40;
Countries of Recruitment:
China
To know more, visit https://www.chictr.org.cn/showproj.html?proj=296804
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