A Randomized, Double-Blind, Parallel Group, Placebo-Controlled Study to Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injection for Post-operative pain following Total Hip Arthroplasty
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- KCT0002653
- Lead Sponsor
- Vivozon
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Terminated
- Sex
- All
- Target Recruitment
- 20
1.Patient between the ages of 25 and 65 years old
2.Male patient, in the case of female patient, postmenopausal women, or women physically incapable of childbearing
3.Subject who underwent surgery specially for the clinical study
4.Ability to provide written informed consent prior to any study procedures.
5.Ability to understand study procedures and communicate clearly with the investigator and staff.
6.Subjects with body weight under 100kg and body mass index (BMI) level lower than 35 kg/m2, inclusive
7.Single-side surgery patient
1.Emergency or unplanned surgery.
2.Repeat operation
< Subject Characteristics >
3.Women with childbearing potential, Women who are pregnant or breastfeeding.
4.Unstable or poorly controlled psychiatric condition (e.g., untreated Post traumatic stress disorder, anxiety, or depression). Subjects who take stable doses of antidepressants and anti-anxiety drugs may be included.
5.Unstable or acute medical condition (e.g., unstable angina, congestive heart failure, renal failure, hepatic failure, AIDS).
6.Subjects who have long Q wave, R wave and S wave (>200msec) or prolonged Corrected QT Interval (> 450msec in male, >470msec in female) at Screening
< Drug, Alcohol, and Pharmacological Considerations >
7.History of alcohol, opiate or other drug abuse or dependence within 12 months prior to Screening .
8.Ongoing or recent (within 6 hour prior to surgery) use of steroids, opioids, or antipsychotics.
9.Alcohol consumption within 24 hours of surgery.
10.Use of nonsteroidal anti-inflammatory drugs (NSAIDs) or acetaminophen within 6 hours of surgery.
11.Use of herbal agents or nutraceuticals (i.e., chaparral, comfrey, germander, jin bu huan, kava, pennyroyal, skullcap, St. John's wort, or valerian) within 7 days prior to surgery.
< Anesthetic and Other Exclusion Considerations >
12.Use of neuraxial or regional anesthesia related to the surgery.
13.Use of ketamine, gabapentin, pregabalin, or lidocaine (>1 mg/kg) intra or peri-operatively, or within 24 hours of surgery.
14.Subject with known allergies to hydromorphone.
15.Subjects who received another investigational drug within 30 days of scheduled surgery
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain Intensity (Numerical Rating Scale, 0-10, NRS at rest)
- Secondary Outcome Measures
Name Time Method Amount of Fentanyl consumption after administration of investigational drug;Amount of relief medication consumed of investigational drug number of requests;Total Amount of Fentanyl consumption and rescue dose;Pain Intensity Difference and Sum Pain Intensity Difference;global measurement of patient satisfaction ;Pharmacokinetics/Pharmacodynamics correlation