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Effect of esticketamine combined with propofol on patients undergoing outpatient hysteroscopic surgery: a randomized controlled trial

Effect of esticketamine combined with propofol on patients undergoing outpatient hysteroscopic surgery: a randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052600
Enrollment
Unknown
Registered
2021-11-02
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Patient with hysteroscopic procedure

Interventions

E1 group:esketamine:0.2mg/kg combine with propofol:2.5mg/kg
E2 group:esketamine:0.3mg/kg combine with propofol:2.5mg/kg
E3 group:esketamine:0.4mg/kg combine with propofol:2.5mg/kg
F group:sufentanil:0.4mg/kg combine with propofol:2.5mg/kg

Sponsors

Hengyang Maternal and Child Health Care Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 45 years, BMI 18-30 kg/m2; 2. ASA I-II.

Exclusion criteria

Exclusion criteria: 1. Hypertension, sinus bradycardia, sinus tachycardia; 2. History of hyperthyroidism; 3. Have neurological or mental diseases; 4. Had taken or was currently taking opioids and non-steroidal anti-inflammatory drugs 48 hours before surgery; 5. Allergic to the study drug Esselketamine or propofol; 6. A history of addiction to opioids and asketamine.

Design outcomes

Primary

MeasureTime frame
Waking time;

Secondary

MeasureTime frame
Number of additional propofol;The original waking time;procedure time;heart rate after entering OR;heart rate 1 minite after induction;BP 1 minite after induction;BP after entering OR;The lowest SPO2;dizzy;VAS score before out of OR;Nausea and vomiting;

Countries

China

Contacts

Public ContactHe Dan

Hengyang Maternal and Child Health Care Hospital

danny_ho@foxmail.com+86 15886421664

Outcome results

None listed

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