ED50 of propofol combined with butorphanol inhibiting response to limb movement in painless abortion

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200059795

Enrollment

Unknown

Registered

2022-05-11

Start date

2022-05-11

Completion date

Unknown

Last updated

2024-04-01

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

Conditions

abortion

Interventions

Group A:0.01 mg butorphanol + propofol

Group B:propofol

Eligibility

Sex/Gender

Female

Age

18 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1. ASA score I or II; 2. 18.0 kg/m2 <= BMI <= 30.0 kg/m2. 3. clinically confirmed early-pregnancy by color doppler ultrasound (< 12 weeks)

Exclusion criteria

Exclusion criteria: 1. Refuse to participate; 2. ASA class III or higher; 3. Allergy to relate durg; 4. Severe liver/kidney/cardiopulmonary/central nervous system dysfunction; 5. A procedure time > 10 min; 6. Long-term take sedative or analgesic medications.

Design outcomes

Primary

Measure	Time frame
Dosage of propofol;	—

Secondary

Measure	Time frame
Heart rate;Breathing;Recovery time;	—

Countries

China

Contacts

Public ContactZhang Zhongqi

Affiliated Shunde Hospital of Jinan University

jxzzq11@139.com+86 137 9868 2324

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026