Evaluation of the Efficacy and Safety of Locally Administered HTX-011 for Postoperative Analgesia Following Bunionectomy

Completed · Phase 2 · Has a placebo group

Conditions studied: Postoperative Pain, Bunions

In brief

A Phase 2, Randomized, Controlled, Multicenter, Evaluation of the Efficacy and Safety of Locally Administered HTX-011 for Postoperative Analgesia Following Bunionectomy

Key facts

Study ID

NCT02762929

Run by

Heron Therapeutics

People needed

430

Starts

2016-05-01

Expected to finish

2017-03-01

Last updated by the study team

2026-02-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be male or female 18 years of age or older
• Female subjects are eligible only if all of the following apply:
• Not pregnant (female subject of child bearing potential must have a negative serum pregnancy test at screening and negative urine pregnancy test before surgery)
• Not lactating
• Not planning to become pregnant while participating in the study
• Be surgically sterile; or be at least two years post-menopausal; or have a monogamous partner who is surgically sterile; or be practicing double-barrier contraception; or practicing abstinence (must agree to use double-barrier contraception in the event of sexual activity); or using an insertable, injectable, transdermal, or combination oral contraceptive approved by the FDA for greater than 2 months prior to screening visits and commits to the use of an acceptable form of birth control for the duration of the study and for 30 days from completion of the study
• Male subjects must be surgically sterile (biologically or surgically) or commit to the use of a reliable method of birth control for the duration of the study until at least 1 week after the administration of study medication
• Be scheduled to undergo a primary unilateral first metatarsal bunionectomy repair, without collateral procedures, under regional anesthesia
• Subject has not had a contralateral bunionectomy in the non-study foot in the past 3 months
• Have the ability and be willing to comply with the study procedures.
• Must be able to understand study procedures and give informed consent for the conduct for all study procedures, using an IRB approved consent form

You may not qualify if…

• Unwilling to sign informed consent or not willing or able to complete all study procedures
• Have a contraindication or be allergic to any medication to be used during the trial period
• Have clinically significant cardiac abnormalities that, in the opinion of the investigator, would pose a health risk to the subject
• Have American Society of Anesthesiologists (ASA) Physical Status classification system category ≥4
• Have clinically significant renal or hepatic abnormalities: for example, AST or ALT > 3x ULN, creatinine > 2x ULN
• Have another pre-existing painful condition that may confound pain assessments
• Have another surgery planned within 30 days of procedure
• Have a known or suspected history of alcohol or drug abuse, or a positive drug screen
• Currently taking analgesics for a chronically painful condition, or has taken long acting opioids within 3 days of surgery, or taken any opioids within 24 hours of scheduled surgery for this study
• Subjects with documented sleep apnea or are on home continuous positive airway pressure (CPAP)
• Subjects who are receiving oxygen therapy at the time of screening
• Have participated in a clinical trial within 30 days of planned surgery

Where it is running

• Study site — Anaheim, California, United States
• Study site — Bakersfield, California, United States
• Study site — Pasadena, Maryland, United States
• Study site — Houston, Texas, United States
• Study site — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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