Randomized controlled trial to measure the Cp50incision of fentanyl with and without flurbiprofen axetil under propofol anesthesia

Randomized controlled trial to measure the Cp50incision of fentanyl with and without flurbiprofen axetil under propofol anesthesia - Randomized controlled trial to measure the Cp50incision of fentanyl with and without flurbiprofen axetil under propofol anesthesia

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000010190

Enrollment

Registered

2013-03-07

Start date

2005-11-29

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

gynecologic laparoscopy

Interventions

With flurbiprofen axetil Without flurbiprofen axetil

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Women (American Society of Anesthesiologists physical status, I&#8211;II; 20&#8211;55 years of age) scheduled to undergo gynecologic laparoscopy were enrolled.

Exclusion criteria

Exclusion criteria: Patients with hepatic or renal disease, those with a body mass index (BMI) >30 kg.m-2, or those taking long-term analgesics were excluded.

Design outcomes

Primary

Measure	Time frame
fentanyl Cp50incision,BIS,BLOOD PRESSURE or HEART RATE	—

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026