Sustained Release Lidocaine for the Treatment of Postoperative Pain

Recruiting Phase 2 Interventional Study
Postoperative Pain Postsurgical Pain
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
19 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
University of British Columbia · Other
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About This Trial
In this study, the investigators are testing a new formulation of lidocaine for its suitability in managing postoperative pain after pelvic (circumcision, inguinal, scrotal), perineal (hemorrhoidectomy) or perianal (fistulotomy) incisions. The new formulation ST-01 is a sustained release lidocaine formulation and is expected to provide pain relief over multiple days. Currently, the drug lidocaine …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Any sex, aged ≥ 19 years * Indication to undergo an operation with a planned pelvic incision * Able and willing to provide informed consent * Stated willingness to comply with all study procedures and availability for the duration of the study * If sexually active, is willing …
Contacts

Lesley Parker

604 875 5594

lparker@sustainedtx.com

CONTACT

Graeme Boniface

604-875-5594

gboniface@prostatecentre.com

CONTACT