Pacira BioSciences, Inc.: all 102 studies

Page 1 of 2. Open to participants first (3), then studies with results posted, then the rest; newest registration first within each.

• A Study to Assess Safety and Tolerability of PCRX-201 in Subjects With Painful Osteoarthritis of the KneeRecruitingNCT06884865Phase 2
• Study to Evaluate the Pharmacokinetics and Safety of EXPAREL for Postoperative Analgesia in Subjects Undergoing Cardiac SurgeryRecruitingNCT06271265Phase 1
• Innovations in Genicular Outcomes RegistryRecruitingNCT05495334
• Phase 3, Sciatic Nerve Block With EXPAREL for Subjects Undergoing BunionectomyCompletedNCT05157841Phase 3Results posted
• Phase 3 Adductor Canal Block With EXPAREL in Subjects Undergoing Primary Unilateral Total Knee ArthroplastyCompletedNCT05139030Phase 3Results posted
• Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of EXPAREL, EXPAREL Admixed With Bupivacaine HCl vs. Bupivacaine HCl Administered as Combined Sciatic and Saphenous Nerve Blocks for Postsurgical Analgesia in Subjects Undergoing Lower Extremity SurgeriesCompletedNCT04518462Phase 3Results posted
• Study to Evaluate the Efficacy and Safety of FX006 in Patients With Glenohumeral Osteoarthritis or Shoulder Adhesive CapsulitisTerminatedNCT04160091Phase 2Results posted
• Study to Evaluate a Procedure for Intra-articular Injection of FX006 in Patients With Osteoarthritis of the HipCompletedNCT04065074Phase 2Results posted
• Phase 4 Study in Adult Subjects Undergoing Posterior Lumbar Spine SurgeriesTerminatedNCT03927911Phase 4Results posted
• Efficacy and Safety of EXPAREL Versus Standard of Care (SoC) in Subjects Undergoing Elective Cesarean SectionCompletedNCT03853694Phase 4Results posted
• Study to Evaluate the Efficacy and Safety of FX006 in Patients With Hip OsteoarthritisTerminatedNCT03793010Phase 3Results posted
• Multicenter Study for Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPARELCompletedNCT03682302Phase 3Results posted
• Study to Evaluate the Effect of FX006 on Synovial Inflammation in Patients With OA of the KneeCompletedNCT03529942Phase 3Results posted
• Study to Compare Exposure of TA Following Administration of FX006 or TAcs in Patients With OA of the Shoulder or HipCompletedNCT03382262Phase 2Results posted
• Study to Compare Exposure of TA Following Administration of Either FX006 or TAcs in Patients With Bilateral Knee OACompletedNCT03378076Phase 2Results posted
• Treatment With Iovera° for Total Knee Arthroplasty (TKA) Post-Operative PainCompletedNCT03327220Not applicableResults posted
• Evaluate the Safety and Efficacy of EXPAREL When Administered Via Infiltration Into the TAP vs. Bupivacaine Alone in Subjects Undergoing Elective C-SectionsCompletedNCT03176459Phase 4Results posted
• Study to Assess the Safety of Repeat Administration of FX006 Administered to Patients With Osteoarthritis of the KneeCompletedNCT03046446Phase 3Results posted
• Phase 4, Controlled Study in Adult Subjects Undergoing Primary, 1-2 Level, Open Lumbar Spinal Fusion SurgeryTerminatedNCT03015961Phase 4Results posted
• Study of Local Administration of DepoTXA for Reduced Postsurgical Bleeding in Subjects Undergoing TKATerminatedNCT02922582Phase 2Results posted
• Study to Assess the Effects of FX006 on Blood Glucose in Patients With OA of the Knee and Type 2 DiabetesCompletedNCT02762370Phase 2Results posted
• Local Infiltration Analgesia With and Without EXPAREL Following Total Knee ArthroplastyCompletedNCT02713490Phase 4Results posted
• Efficacy, Safety, and Pharmacokinetics of Brachial Plexus Block With EXPAREL in Shoulder SurgeryCompletedNCT02713230Phase 3Results posted
• Efficacy, Safety, and Pharmacokinetics of Femoral Nerve Block With EXPAREL in Total Knee ArthroplastyCompletedNCT02713178Phase 3Results posted
• Study to Characterize the PK and Local Extent and Duration of Exposure From FX006 in Patients With OA of the KneeCompletedNCT02637323Phase 2Results posted
• Evaluation of EXPAREL for Prolonged Postsurgical Analgesia in Subjects Undergoing Third Molar ExtractionCompletedNCT02517905Phase 3Results posted
• Proof of Concept Study Comparing FX006 to Kenalog®-40 in Patients With Post-Traumatic Osteoarthritis of the KneeTerminatedNCT02468583Phase 2Results posted
• Study of FX006 for the Treatment of Pain in Patients With Osteoarthritis of the KneeCompletedNCT02357459Phase 3Results posted
• Evaluation of the Safety and Efficacy of EXPAREL When Administered Into the TAP in Subjects Undergoing Cesarean SectionTerminatedNCT02353754Phase 4Results posted
• Pharmacokinetics and Safety of Bupivacaine HCl Spinal Block and EXPAREL Local Infiltration in Total Knee ArthroplastyCompletedNCT02284386Phase 4Results posted
• A Randomized, Study to Evaluate the Iovera° Device in Treating Pain Associated With Total Knee ArthroplastyCompletedNCT02284113Not applicableResults posted
• Study to Evaluate the Iovera° Device for Temporary Relief From Knee PainCompletedNCT02260921Not applicableResults posted
• EXPAREL Infiltration in Subjects Undergoing Femoral Nerve Block With Bupivacaine HCl for Total Knee ArthroplastyCompletedNCT02255500Phase 4Results posted
• Safety and Pharmacokinetics Study of Redosing EXPAREL in Healthy VolunteersCompletedNCT02210247Phase 1Results posted
• Pharmacokinetic Evaluation of EXPAREL in Adults Undergoing TonsillectomyCompletedNCT02199574Phase 4Results posted
• Study of FX006 vs Normal Saline in Patients With Osteoarthritis of the KneeCompletedNCT02116972Phase 2Results posted
• A Health Economic Trial in Adult Patients Undergoing Laparoscopic ColectomyTerminatedNCT02058290Phase 4Results posted
• Study to Characterize the Local Duration of Exposure From FX006 in Patients With Osteoarthritis of the KneeCompletedNCT02003365Phase 2Results posted
• EXPAREL Administered Into the TAP for Analgesia in Subjects Undergoing Open Total Abdominal HysterectomyTerminatedNCT01919606Phase 4Results posted
• EXPAREL Administered by Infiltration Into the TAP for Prolonged Postsurgical Analgesia in Lower Abdominal SurgeriesTerminatedNCT01919190Phase 4Results posted
• Study Evaluating Treatment of Upper Limb Spasticity Using the Cryo-Touch III DeviceCompletedNCT01863901Not applicableResults posted
• Intercostal Nerve Block With Liposome Bupivacaine in Subjects Undergoing Posterolateral ThoracotomyCompletedNCT01802411Phase 3Results posted
• EXPAREL Infiltrated Into the TAP for Postoperative Analgesia in Unilateral Abdominal Hernia RepairCompletedNCT01801124Phase 4Results posted
• Study Evaluating the Treatment of Occipital NeuralgiaCompletedNCT01753765Not applicableResults posted
• A Prospective Study Evaluating the Treatment of Knee Osteoarthritis With the Cryo-Touch III DeviceCompletedNCT01704157Not applicableResults posted
• Femoral Nerve Block With Liposome Bupivacaine for Postsurgical Analgesia Following Total Knee ArthroplastyCompletedNCT01683071Phase 2/3Results posted
• Probe Configuration and Time-Temperature Dose Ranging for Understanding of Skin Lesion EffectsCompletedNCT01681745Not applicableResults posted
• Study of EXPAREL in Patients Undergoing Breast AugmentationCompletedNCT01582490Phase 4Results posted
• TAP-patients With Robotic Assisted Lap ProstatectomyCompletedNCT01582477Phase 4Results posted
• A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B504CompletedNCT01509807Phase 4Results posted
• A Health Economic Trial in Adult Patients Undergoing Ileostomy Reversal MA402S23B501CompletedNCT01509638Phase 4Results posted
• Adult Patients Undergoing Open Colectomy MA402S23B303CompletedNCT01507246Phase 4Results posted
• A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B302TerminatedNCT01507233Phase 4Results posted
• A Health Economic Trial in Adult Patients Undergoing Open Colectomy MA402S23B301TerminatedNCT01507220Phase 4Results posted
• Pharmacokinetic and Pharmacodynamic Study of FX006 in Patients With Osteoarthritis of the KneeCompletedNCT01487200Phase 2Results posted
• Study of FX006 in Patients With Osteoarthritis of the KneeCompletedNCT01487161Phase 2Results posted
• Evaluation of the Safety and Efficacy of a Single Dose of SKY0402 in Subjects Undergoing Augmentation MammoplastyCompletedNCT01206608Phase 2Results posted
• Safety, Efficacy, and Pharmacokinetics of SKY0402 Administered as a Nerve Block in Subjects Undergoing BunionectomyCompletedNCT01206595Phase 2Results posted
• Evaluation of the Safety, Efficacy, and Pharmacokinetics of SKY0402 in Subjects Undergoing Inguinal Hernia RepairCompletedNCT01203644Phase 2Results posted
• Cryo-Touch II for the Treatment of WrinklesCompletedNCT01167140Phase 2/3Results posted
• Observational Study to Assess Long-Term Follow-Up of Breast Augmentation SubjectsCompletedNCT01076686Results posted
• Study of Pain Control in HemorrhoidectomyCompletedNCT00890721Phase 3Results posted
• Study of Postoperative Analgesia in BunionectomyCompletedNCT00890682Phase 3Results posted
• Phase 3 Study of Local Administration of SKY0402 for Postoperative Analgesia in Subject Undergoing Breast AugmentationTerminatedNCT00813111Phase 3Results posted
• Dose Finding Posterolateral Thoracotomy StudyTerminatedNCT00807209Phase 2Results posted
• A Phase 3 Study to Evaluate the Safety and Efficacy of SKY0402 in Subjects Undergoing Total Knee ArthroplastyCompletedNCT00745290Phase 3Results posted
• Study to Evaluate Postoperative Analgesia in Subjects Undergoing HemorrhoidectomyCompletedNCT00744848Phase 3Results posted
• Phase 2 Dose-Ranging Study of SKY0402 for Prolonged Postoperative Analgesia in Subject Undergoing HemorrhoidectomyCompletedNCT00529126Phase 2Results posted
• Dose-Ranging Study for Prolonged Postoperative Analgesia in Subject Undergoing Total Knee ArthroplastyCompletedNCT00485693Phase 2Results posted
• Dose-ranging Study for Postoperative Analgesia in Subjects Undergoing Primary Unilateral Inguinal Hernia RepairCompletedNCT00485433Phase 2Results posted
• A Study to Evaluate an Intra-Articular Injection of ZILRETTA Versus Triamcinolone Acetonide, Immediate Release in Subjects With Osteoarthritis of the HipTerminatedNCT06977568Phase 2
• Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity SpasticityActive, not recruitingNCT06340451Not applicable
• ZILRETTA in Subjects With Shoulder OsteoarthritisActive, not recruitingNCT06269705Phase 3
• Phase 1, Dose Escalation Study to Evaluate of Safety, Pharmacokinetics and Pharmacodynamics of Liposomal Bupivacaine 13.3 Administered Via a Single Intrathecal Injection to Healthy VolunteersCompletedNCT05456490Phase 1
• Study to Evaluate the Safety and Tolerability of FX301 in Patients Undergoing BunionectomyCompletedNCT04826328Phase 1
• Study to Evaluate the Pharmacokinetics and Safety of EXPAREL Administered as a Pectoral Plane Block in Women Undergoing Breast AugmentationCompletedNCT04293809Phase 1
• Study to Evaluate Iovera®° in Adult Patients Undergoing Total Knee ArthroplastyTerminatedNCT04191031Not applicable
• Evaluation of Safety, Pharmacokinetics and Pharmacodynamics of EXPAREL® Administered Via a Single Intrathecal Injection to Healthy VolunteersTerminatedNCT04173611Phase 1
• Study to Evaluate the Safety and Tolerability of FX201 in Patients With Osteoarthritis of the KneeActive, not recruitingNCT04119687Phase 1
• Study to Evaluate the Pharmacokinetics, Pharmacodynamics and Safety, of EXPAREL Administered as Sciatic Nerve Block (In Popliteal Fossa), for Postsurgical Analgesia in Subjects Undergoing BunionectomyCompletedNCT04002089Phase 1
• EXPAREL Facia Iliaca Compartment Block for Intertrochanteric Hip FractureWithdrawnNCT03955458Phase 4
• Phase 3, Randomized, Double Blinded, Active Controlled, Multicenter Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of EXPAREL Admixed With Bupi vs. Bupi Only Administered as Combined Sciatic and Adductor Canal Nerve Block for Postsurgical Analgesia in Lower Extremity SurgeriesWithdrawnNCT03954639Phase 3
• Evaluate the Iovera° Device in Treating Pain Associated With Anterior Cruciate Ligament ReconstructionWithdrawnNCT03909516Not applicable
• Iovera° to Treat Pain Associated With ACL Reconstruction and RehabilitationWithdrawnNCT03688477Not applicable
• Study in Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPARELCompletedNCT03485014Phase 1
• Study in Adult Subjects Undergoing Posterolateral ThoracotomyTerminatedNCT03428984Phase 1
• PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive SurgeryCompletedNCT02985762Phase 1
• Pain Control in Bariatric Patients: EXPAREL(R) vs. the On-Q(R) Pain BallCompletedNCT02142829Phase 4
• Prospective Study Evaluating the Treatment of Hyperdynamic Forehead WrinklesCompletedNCT01984619
• Effectiveness and Safety Study of the Iovera Device for the Temporary Reduction in the Appearance of Forehead WrinklesCompletedNCT01950065Not applicable
• Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the CRYO-TOUCH III DeviceCompletedNCT01808742
• A Prospective Study Evaluating the Treatment of Forehead and/or Glabellar Lines With the Cryo-Touch IV DeviceCompletedNCT01801826
• Study Evaluating Treatment of Forefoot Pain Related to Nerve Entrapment Using the Cryo-Touch III DeviceCompletedNCT01753778Not applicable
• A Study to Evaluate the Safety and Effectiveness of the Cryo-Touch II Device for the Treatment of Forehead and/or Glabellar LinesCompletedNCT01447342Phase 2/3
• Cryo-Touch III Refinement Study Investigational PlanCompletedNCT01379365Phase 2/3
• Study of FX005 for the Treatment of Pain in Patients With Osteoarthritis of the KneeCompletedNCT01291914Phase 1/2
• Study of the MyoScience Tissue Remodeling Device for Facial RejuvenationCompletedNCT00842062Phase 1/2
• Hepatic Impairment Study: Pharmacokinetics in Healthy and Hepatically Impaired SubjectsCompletedNCT00812305Phase 1
• Evaluate the Onset of Action of SKY0402 Following Local Infiltration in Healthy VolunteersCompletedNCT00806806Phase 1
• Phase 1 Thorough QT Study in Young Healthy VolunteersCompletedNCT00485667Phase 1

← Pacira BioSciences, Inc. overview and focus areas