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A prospective, randomized controlled clinical trial: comparison of the analgesia effects between patient-control intravenous analgesia (PCIA) combinations of flurbiprofen with dezocine based on patient-control intravenous analgesia (PCIA) following lobectomy

A prospective, randomized controlled clinical trial: comparison of the analgesia effects between patient-control intravenous analgesia (PCIA) combinations of flurbiprofen with dezocine based on patient-control intravenous analgesia (PCIA) following lobectomy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018563
Enrollment
Unknown
Registered
2018-09-25
Start date
2018-11-01
Completion date
Unknown
Last updated
2018-10-01

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

Conditions

pulmonary disease

Interventions

Group A: PCIA + Flurbiprofen axetil 50mg
Group B:PCIA+ dezocine 5mg
Group C:PCIA + flurbiprofen axetil 50mg+ dezocine 5mg
Group D:PCIA + flurbiprofen axetil 25mg+ dezocine 2.5mg

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 70 years; 2. Male: weight =45kg, female: weight =42kg; 3. Patients undergoing pulmonary lobectomy surgery; 4. ASA scores I-II grade; 5. Known numeric rating scales (NRS); 6. Known how to use patient-controlled intravenous analgesia (PCIA); 7. Had essential complete materials such as clinical staging of lung cancer and medications situation; 8. Willing to participant after reading and signing an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Time for smoking cessation <2 weeks; 2. Patients undergoing other pulmonary operations rather than lobectomy; 3. Patient with allergies to opioids, non-steroidal anti-inflammatory drugs (NSAIDs); 4. Patients were pregnant or breastfeeding women; 5. Patients with preoperative severe mental illness; 6. Patients with preoperative gastrointestinal or blood system disease; 7. Patients with grade 3 hypertension; 8. Patients underwent cardiac ischemia; 9. Patients received preoperative radiotherapy or neoadjuvant chemotherapy; 10. The investigator judges that the patient is not suitable for inclusion in the trial.

Design outcomes

Primary

MeasureTime frame
The numeric rating scales (NRS);the total consumption of sufentanil after operations;incidence of experimental drug-related adverse effects: nausea, vomiting, dizziness, fatigue, drowsiness, pruritus, abdominal distention, bloating, constipation, euphoria, respiratory depression and indigestion;

Secondary

MeasureTime frame
the analgesia cost;chest tube duration;length of hospital stay;gastrointestinal exhaust time;the serum level of interleukin-1ß (IL-1ß), IL-6, IL-8, IL-2, tumor necrosis factor-a (TNF-a), C-reactive protein (CRP)?prostaglandin E2 (PGE2)?5-hydroxytryptamine (5-HT);dezocine additional time,times,additional quantity;postoperative time to get out of bed;

Countries

China

Contacts

Public ContactLunxu Liu

West China Hospital, Sichuan University

lunxu_liu@aliyun.com+86 18980601525

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026