Evaluate the Onset of Action of SKY0402 Following Local Infiltration in Healthy Volunteers

Postoperative Pain Management Clinical Trial

— TTO  

Official title:

A Phase 1 Randomized, Single-blind, Sequential Cohort, Crossover Study to Evaluate the Onset of Action of SKY0402 Following Local Infiltration in Healthy Volunteers

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00806806
• Other study ID #: SKY0402C109
• Status: Completed
• Phase: Phase 1
• First received: December 9, 2008
• Last updated: August 31, 2010
• Start date: October 2008
• Est. completion date: February 2009

Study information

• Verified date: August 2010
• Source: Pacira Pharmaceuticals, Inc
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Given as a single perioperative injection, SKY0402 could provide adequate, continuous, and extended pain relief that could greatly simplify postoperative pain management, reduce the need for repeated administration, and minimize episodes of breakthrough pain.

Description:

Subjects will be given either SKY0402 or placebo in response to a noxious stimulus, and the time to onset will be recorded.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 128
• Est. completion date: February 2009
• Est. primary completion date: February 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 55 Years

Eligibility

Inclusion Criteria:

Subjects eligible for study entry will meet the following criteria:

• Male or female, ages at least 18 years and not over 55 years.

• Body mass index (BMI) within the range 20.0 to 30.0 kg/m2, inclusive.

• Applies to females only: Female subjects of childbearing potential with a nonsterilized male sexual partner must agree to use a hormonal contraceptive, barrier contraceptive with additional spermicide, or an intrauterine device beginning > 30 days prior to the first dosing and continuing until > 7 days after the end of the study. Female subjects who are postmenopausal must have been postmenopausal for > 1 year if they wish not to use contraceptives.

• Good general health, evidenced by a lack of significantly abnormal findings on medical history and screening assessments.

• Pain intensity score of > 30 mm on a VAS after incision and application of an 18% acetic acid solution to nontreated skin (i.e., not infiltrated with any test or control article) at Screening.

• Able and willing to comply with all study visits and procedures, including returning as scheduled for the second treatment visit.

• Able to speak, read, and understand the language of the ICF, study questionnaires, and other instruments used for collecting subject-reported outcomes, in order to enable accurate and appropriate responses to pain scales and other required study assessments.

• Willing and capable of providing written informed consent.

Exclusion Criteria:

A subject will not be eligible for the study if he or she meets any of the following criteria:

• A history of hypersensitivity to amide type local anesthetics.

• Pregnancy, nursing, or planning to become pregnant during the course of the study.

• Any current conditions that might interfere with pain assessments, including current pain.

• Conditions of the skin or neurological abnormalities that might alter pain sensitivity. These include excessive scarring, burns, skin grafts, and trauma. Tattoos are permitted.

• A history of keloid formation.

• A coagulopathy or use of medications that might enhance bleeding.

• Use of any of the following medication within the times specified before study drug administration:

• Long-acting opioid mediations within 3 days.

• Any opioid medication within 24 hours.

• Any analgesic medication within 12 hours.

• Consumption of alcohol within 24 hours before either treatment visit.

• Any condition that, in the opinion of the Investigator, renders a subject unsuitable for participation in the study. NOTE: The specific reason(s) for exclusion will be documented in the Screening Log.

• Administration of an investigational drug within 30 days or 5 elimination half-lives of such investigational drug, whichever is longer, prior to study drug administration, or planned administration of another investigational product or procedure during the subject's participation in this study.

Minor deviations in eligibility criteria are permitted if approved by the Pacira Medical Monitor in agreement with the Investigator prior to dosing.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain Management

Intervention

Drug:
• SKY0402
Local administration of SKY0402 followed by noxious stimulus
• Placebo
Local administration of Placebo followed by noxious stimuli

Locations

Country	Name	City	State
United States	The Ohio State University College of Medicine, Dept of Pharmacology	Columbus	Ohio

Sponsors (1)

Lead Sponsor	Collaborator
Pacira Pharmaceuticals, Inc

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	time to onset of action		15 minutes	Yes
Secondary	time to onset		bewteen 15 and 30 minutes	Yes