Pacira BioSciences, Inc.: Pain, Postoperative trials
The registry lists 22 Pain, Postoperative studies with Pacira BioSciences, Inc. as lead sponsor. 1 are open to participants now and 15 have results posted.
Phase 1 6Phase 2 6Phase 3 4Phase 4 5No phase 2(a study in two phases counts in both)
Studies
Open to participants first, then studies with results posted, then the rest; newest registration first within each.
- Study to Evaluate the Pharmacokinetics and Safety of EXPAREL for Postoperative Analgesia in Subjects Undergoing Cardiac SurgeryRecruitingNCT06271265Phase 1
- Phase 4 Study in Adult Subjects Undergoing Posterior Lumbar Spine SurgeriesTerminatedNCT03927911Phase 4Results posted
- Multicenter Study for Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPARELCompletedNCT03682302Phase 3Results posted
- Phase 4, Controlled Study in Adult Subjects Undergoing Primary, 1-2 Level, Open Lumbar Spinal Fusion SurgeryTerminatedNCT03015961Phase 4Results posted
- EXPAREL Administered Into the TAP for Analgesia in Subjects Undergoing Open Total Abdominal HysterectomyTerminatedNCT01919606Phase 4Results posted
- Intercostal Nerve Block With Liposome Bupivacaine in Subjects Undergoing Posterolateral ThoracotomyCompletedNCT01802411Phase 3Results posted
- Femoral Nerve Block With Liposome Bupivacaine for Postsurgical Analgesia Following Total Knee ArthroplastyCompletedNCT01683071Phase 2/3Results posted
- Study of EXPAREL in Patients Undergoing Breast AugmentationCompletedNCT01582490Phase 4Results posted
- TAP-patients With Robotic Assisted Lap ProstatectomyCompletedNCT01582477Phase 4Results 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
- Observational Study to Assess Long-Term Follow-Up of Breast Augmentation SubjectsCompletedNCT01076686Results 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
- 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
- Study to Evaluate the Safety and Tolerability of FX301 in Patients Undergoing BunionectomyCompletedNCT04826328Phase 1
- Study to Evaluate Iovera®° in Adult Patients Undergoing Total Knee ArthroplastyTerminatedNCT04191031Not applicable
- Study in Pediatric Subjects Evaluating Pharmacokinetics and Safety of EXPARELCompletedNCT03485014Phase 1
- Study in Adult Subjects Undergoing Posterolateral ThoracotomyTerminatedNCT03428984Phase 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