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Perioperative standardized analgesia with flurbiprofen axetil on enhanced recovery after surgery: a randomized, double-blind, controlled study

The effect of perioperative flurbiprofen axetil standardized analgesia on postoperative accelerated recovery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053178
Enrollment
Unknown
Registered
2021-11-13
Start date
2021-11-10
Completion date
Unknown
Last updated
2022-09-20

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

Conditions

perioperative pain

Interventions

Group 1:Standardized analgesia with flurbiprofen ester
Group 2:Placebo standardized analgesia
Group 3:None

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 65 to 80 years, gender is not limited; 2. ASA IIII grade; 3. Body mass index (BMI) 18-30kg/m^2; 4. General anesthesia surgery, the operation time is 1 to 6 hours; 5. The patients agreed to participate in this study and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Active peptic ulcer disease; 2. Significant abnormalities in the coagulation system and bleeding tendency; 3. Obvious abnormality of liver and kidney function (relevant indicators exceed the upper limit of normal by more than 2 times); 4. Aspirin asthma or allergic to non-steroidal anti-inflammatory drugs; 5. Are using quinolone antibiotics (such as enoxacin, lomefloxacin, norfloxacin, etc.); 6. Patients with heart failure are using furosemide; 7. Hypertension grade III; 8. Patients who are pregnant or breastfeeding.

Design outcomes

Primary

MeasureTime frame
Postoperative Recovery Assessment Scale;

Secondary

MeasureTime frame
Visual Analog Pain Score;

Countries

China

Contacts

Public ContactZheng Xiaochun

Fujian Provincial Hospital

zhengxc2@163.com+86 13705058351

Outcome results

None listed

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