Pain
Conditions
Brief summary
A multicenter, randomized, double-blind, placebo-controlled, dose-exploratory phase II clinical trial to evaluating the efficacy and safety of Felbinac Trometamol Injection in the treatment of moderate to severe pain after surgery.Main purpose is preliminary evaluation the effectiveness of Felbinac Trometamol Injection in the treatment of moderate and severe pain after surgery.Secondary purpose is to explore the dosage regimen of Felbinac Trometamol Injection in the treatment of moderate and severe pain after surgery, and provide data support for later clinical trial.
Interventions
Felbinac Trometamol Injection diluted to 100 ml with 0.9% sodium chloride injection,a 30-minute period using a Microinjection pump. One dose at 8h and 16h after the start of the first dose,the first intravenous infusion was started at the end of the operation (Skin suture completes the last stitch).the drug was given 3 times,3 times/day,once every 8 hours.
DRUGPlacebos
Placebo diluted to 100 ml with 0.9% sodium chloride injection,a 30-minute period using a Microinjection pump. One dose at 8h and 16h after the start of the first dose,the first intravenous infusion was started at the end of the operation (Skin suture completes the last stitch).the drug was given 3 times,3 times/day,once every 8 hours.
Sponsors
Shijiazhuang Yiling Pharmaceutical Co. Ltd
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* 18≤age≤65 years of age, gender is not limited; * ASA grade I or II; * 18 ≤ body mass index (BMI) ≤ 30 \[BMI = weight (kg) / height 2 (m2)\]; * Inpatients who underwent open surgery under elective general anesthesia (including gallbladder, intestinal or lower abdominal surgery, etc.), or laparoscopic surgery with a single surgical incision ≥ 5 cm; * Expected to require more than 24 hours of PCIA( patient controlled intravenous analgesia) treatment after surgery ; * Ability to understand research procedures and pain scales, operate PCIA devices, and communicate effectively with researchers; * Agree to participate in the trial and voluntarily sign the informed consent form.
Exclusion criteria
* Those who have a history of chronic pain for more than 3 months or who are undergoing regular analgesia for more than 3 months; * Those who used other analgesics, muscle relaxants or sedatives within 24 hours before operation (excluding those required for this operation), or those who used long-acting non-steroidal anti-inflammatory drugs (NSAIDs) within 12 hours, or those who used short-acting non-steroidal anti-inflammatory drugs (NSAIDs) within 6 hours before operation(See Annex 1). * A person with high bleeding risk, and also including who with congenital bleeding disorders (such as hemophilia), thrombocytopenia (PLT \< 80 × 10 ∧ 9 / L), abnormal platelet function (such as idiopathic thrombocytopenic purpura, disseminated intravascular coagulation, congenital platelet dysfunction, etc.) or any clinically significant active bleeding, coagulopathy; * A person who received full-dose anticoagulant therapy, activated protein C or thrombolytic drugs within 6 hours before surgery (except for heparin subcutaneous injection for preventive treatment); * People with heart failure (NYHA grade III or IV), unstable angina pectoris, acute myocardial infarction, and severe arrhythmia within 6 months before surgery * Hypertensive patients who have not been satisfactorily controlled by blood pressure (systolic blood pressure ≥160mmHg or diastolic blood pressure ≥105mmHg), or ACEI/diuretics for ≥30 days, or hypotension (systolic blood pressure \<90mmHg); * People with bronchial asthma, pulmonary heart disease or other serious respiratory diseases; * Person with gastrointestinal ulcer and a history of gastrointestinal bleeding 6 weeks before operation and required medical treatment; * Those with previous cerebral arteriovenous malformations, cerebral aneurysms, brain tumors, or preoperative traumatic brain injury, intracranial surgery, history of stroke; * Patients with poor glycemic control of diabetes (random blood glucose \> 11.1mmol / L); * Patients with autoimmune diseases, connective tissue diseases, etc. who need long-term use of adrenocortical hormone therapy; * Abnormal liver and kidney function: ALT/AST\> 2 times the upper limit of normal value, or creatinine\> upper limit of normal value, or dialysis treatment within 28 days before surgery; * Allergic constitution, or known to be allergic to this drug, NSAIDs, and opioids; * Patients who are afflicted with narcotic drugs, drugs, or resistant to opioids; * A woman who is breast-feeding or pregnant, who is unable or unwilling to follow the investigator's guidance during the study period and within 3 months after the last study treatment; * Those who have participated in other clinical trials within 3 months before surgery; * Investigators believe that it is not suitable for participating in this research.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 24h total morphine consumption | up to 24hours after multi-dose | The the total amount of morphine within 24 hours after the end of first drug administration |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Area under the pain intensity curve(AUC) | up to 24 hours after multi-dose | Pain intensity under exercise/rest state - area under the time curve |
| Press time | up to 24 hours after multi-dose | The first time to press the analgesic pump for analgesia |
| Total number of analgesia pump presses | up to 24 hours after multi-dose | Total number of analgesic pump presses within 24 hours after the first dose |
| The number of effective presses of analgesia pump | up to 24 hours after multi-dose | The number of effective presses of analgesia pump within 24 hours after the end of the first dose |
Countries
China
Outcome results
None listed