The effect of flurbiprofen axetil in induced abortion under intravenous anesthesia

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900022578

Enrollment

Unknown

Registered

2019-04-17

Start date

2019-04-22

Completion date

Unknown

Last updated

2019-04-23

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

Conditions

Abortion

Interventions

control:none

Experimental group:flurbiprofen

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: ASA I-II, elective induced abortion

Exclusion criteria

Exclusion criteria: asthma, flurbiprofen allergy, gastrointestinal ulcer, mental illness

Design outcomes

Primary

Measure	Time frame
Pain assessment;	—

Contacts

Public ContactZifeng Xu

the International Peace Maternity and Child Health Hospital, Shanghai Jiao Tong University School of Medicine

xuzf@shsmu.edu.cn+86 021-64070434

Outcome results

None listed

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