Lotus Clinical Research, LLC

Pasadena, California 91105

1 studies enrolling now · 27 studies all time

What they study most

Abdominoplasty, Acute Pain, Anesthesia, Assessing Injection Pain of Makena® (Hydroxyprogesterone Caproate Injection, 250 mg/mL) in Healthy Post-menopausal Women, Bunion, Chronic Nonmalignant and Nonneuropathic Pain, Delayed Onset Muscle Soreness, Dental Pain, Hallux Valgus Deformity, Laparoscopic Surgery, Lumbar Laminectomy, Mild or Moderate Surgical Bleeding

Studies at this site

• Phase 3 Herniorrhaphy Study for Postoperative Analgesia (EPOCH 2) — Completed
• Phase 2 Herniorrhaphy Study for Opioid Elimination — Completed
• Efficacy and Safety of HSK3486 Compared to Propofol in Induction of General Anesthesia in Adults Having Elective Surgery — Completed
• Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears — Running, not enrolling
• A Longitudinal, Multi-Center Safety Study of Autologous Adult Adipose-Derived Regenerative Cell Injection Into Chronic Partial-Thickness Rotator Cuff Tears — Enrolling by invitation
• A Study to Evaluate the Efficacy and Safety of K-285 Compared With Menthol Gel for the Treatment of Delayed Onset Muscle Soreness (DOMS) in the Lower Extremity — Stopped early
• Study in Subjects Undergoing Complete Abdominoplasty — Completed
• HTX-011 in Spinal Surgery — Completed
• Study Assessing Injection Pain of Makena® (Hydroxyprogesterone Caproate Injection, 250 mg/mL) When Administered Via Subcutaneous Auto-injector vs Intramuscular Injection Via Needle and Syringe in Healthy Post-menopausal Women — Stopped early
• Open-Label CA-008 (Vocacapsaicin) in Bunionectomy — Completed
• Study of CA-008 (Vocacapsaicin) in Bunionectomy Patients — Completed
• A Phase 1 Study of Intraoperative Administration of CA-008 for the Correction of Hallux Valgus Deformity — Completed
• Long-term Safety of Once-daily Hydrocodone Bitartrate (HYD) Tablets For Moderate to Severe Chronic Nonmalignant and Nonneuropathic Pain. Includes a 24-week Extension Period. — Completed
• A Study of Fibrocaps™ in Surgical Bleeding — Completed
• Study to Evaluate Botulinum Neurotoxin Serotype E (EB-001) in Reducing Musculoskeletal Pain in Abdominoplasty — Stopped early
• Phase II Study of AP0302 5% Versus a Vehicle Comparator — Completed
• Study of Buprenorphine Sublingual Spray Versus Standard of Care Narcotic Therapy for the Treatment of Post-Operative Pain — Completed
• Evaluation of N1539 Following Abdominoplasty Surgery — Completed
• Placebo-Controlled Evaluation of Intranasal Dexmedetomidine for Postoperative Analgesia Following Bunionectomy Surgery — Completed
• Safety and Efficacy of COV795 in Moderate to Severe Post-Operative Bunionectomy Pain With an Open-label Extension — Completed
• Safety and Efficacy Study of COV155 for Post-operative Bunionectomy Pain — Completed
• A Randomized, Open Label, Prospective Study to Explore the Clinical Characteristics of Oral MNK155 and Norco 7.5mg/325 When Used for the Treatment of Moderate to Severe Post Operative Pain — Stopped early
• Placebo-Controlled Evaluation of Intranasal Dexmedetomidine for Postoperative Analgesia Following Bunionectomy — Stopped early
• Methodological Validation of Ibuprofen Verses Placebo for Post Operative Pain After Third Molar Extraction Surgery — Completed
• An Investigator Initiated, Within-Subject, Proof of Concept Study to Assess the Efficacy and Safety of Voltaren Gel in Subjects With DOMS — Completed
• A Study to Assess the Analgesic Properties of a Sublingual Wafer Formulation of Ketamine Following Third Molar Extraction — Completed
• Efficacy, Safety and Tolerability Study of N1539 in Subjects After Abdominal Laparoscopic Surgery — Stopped early