Status:
COMPLETED
Study in Subjects Undergoing Complete Abdominoplasty
Lead Sponsor:
Concentric Analgesics
Conditions:
Postsurgical Pain
Eligibility:
All Genders
18-65 years
Phase:
PHASE2
Brief Summary
Phase 2, single center, randomized, double-blind, placebo-controlled, parallel design study of CA-008 vs. placebo in subjects undergoing an elective C-ABD under general anesthesia supplemented with a ...
Detailed Description
This is a Phase 2, single-center, randomized, double-blind, placebo-controlled, parallel design study evaluating up to 4 ascending dose level cohorts, each evaluating a single dose of CA-008 vs. place...
Eligibility Criteria
Inclusion
- Key
- Plan to undergo an elective complete abdominoplasty (C-ABD), without collateral procedure or additional surgeries.
- In the medical judgment of the investigator, be a reasonably healthy adult aged 18 - 65 years old, inclusive, and American Society of Anesthesiology (ASA) physical Class 1 or 2 at the time of randomization.
- Unless the subject has a same sex partner, he or she must either be sterile (surgically or biologically) or commit to an acceptable method of birth control while participating in the study.
- Have a body mass index ≤ 35 kg/m².
- Be willing and able to sign the informed consent form (ICF) approved by an Institutional Review Board (IRB).
- Key
Exclusion
- In the opinion of the Investigator, have a concurrent painful condition that may require analgesic treatment during the study period or may confound post-surgical pain assessments.
- Have a known allergy to chili peppers, capsaicin or the components of CA-008, acetaminophen, bupivacaine, fentanyl hydromorphone or oxycodone.
- As determined by the investigator have a history or clinical manifestation of significant medical, neuropsychiatric or other condition, including a clinically significant existing arrhythmia, left bundle branch block or abnormal ECG, myocardial infarction or coronary arterial bypass graft surgery within the prior 12 months, significant abnormal clinical laboratory test value, or known bleeding abnormality that could preclude or impair study participation or interfere with study assessments.
- The following are considered disallowed medications:
- Be tolerant to opioids defined as those who have been receiving or have received chronic opioid therapy greater than 15 mg of oral morphine equivalents per day for greater than 3 out of 7 days per week over a one-month period within 6 months of screening.
- Within 1 day prior to surgery and throughout the inpatient period, be taking any capsaicin-containing products, such as dietary supplements or over-the-counter (OTC) preparations, including topical formulations, and prescription medications.
- Within the 7 days prior to surgery, be taking any central nervous system (CNS) active agent as an analgesic adjunct medication, such as anticonvulsants, antidepressants, benzodiazepines, sedative- hypnotics, clonidine and other central alpha-2 agents, ketamine or muscle relaxants.
- i. These drugs are permitted if prescribed for non-pain indications and the dose has been stable for at least 30 days prior to surgery.
- ii. The use of benzodiazepines and the non-benzodiazepines are permitted to treat insomnia during the postoperative period.
Key Trial Info
Start Date :
December 3 2018
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 12 2019
Estimated Enrollment :
54 Patients enrolled
Trial Details
Trial ID
NCT03789318
Start Date
December 3 2018
End Date
June 12 2019
Last Update
March 19 2024
Active Locations (1)
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1
Lotus Clinical Research, LLC
Pasadena, California, United States, 91105