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Clinical Trials for Nociceptive Pain

• Opioid Sparing Anesthesia in Cervical Spine Surgery
• A Study of the Effects of Intravenous Magnesium Sulphate on Anaesthesia and Analgesia in Elective General Surgery Patients
• Opioid Sparing Anesthesia in Lumbar Spine Surgery
• The Impact of Esmolol Administration on Postoperative Recovery
• Opioid-free Anesthesia in Thyroidectomies
• Opioid-free Anesthesia With a Mixture of Dexmedetomidine-lidocaine-ketamine
• NOL Index to Compare the Intraoperative Analgesic Effect of Propofol Versus Sevoflurane
• PET/MRI in the Diagnosis of Pediatric Chronic Pain
• A Study to Evaluate the Safety and Pharmacokinetics of CNTX-6016 in Healthy Subjects
• Pain Response to Cannabidiol in Opioid-induced Hyperalgesia, Acute Nociceptive Pain and Allodynia By Using a Model Mimicking Acute Pain in Healthy Adults
• Pain Response to Cannabidiol in Induced Acute Nociceptive Pain, Allodynia and Hyperalgesia By Using a Model Mimicking Acute Pain in Healthy Adults
• Effect of Dexmedetomidine on Nol-Index Guided Remifentanil Analgesia
• Comparison of the Efficacy, Tolerability and Safety of actiTENS to Those of Level 2 Analgesic Treatments.
• Comparison of Postoperative Nociception Between NOL-guided and Standard Intraoperative Analgesia Based on Fentanyl
• Comparation Analgesia Efficiency With Propofol Combine Sevoflurane vs Propofol
• A Placebo-Controlled, Two-Part Study, Oral Dose to Evaluate the Safety, Pharmacokinetics, and Pharmacodynamics of CNTX-6970 in Healthy Subjects
• Automatic Remifentanil Administration Guided by ANI During Propofol Anesthesia
• PET/MRI in the Diagnosis of Chronic Pain
• Determine the Effect of AZD3161,Injected Intradermally, on Quantitative Sensory Testing Variables in Normal and Ultraviolet-C (UVC) Exposed Skin in Healthy Volunteers
• Evaluation of Effectiveness and Tolerability of Tapentadol Hydrochloride in Subjects With Severe Chronic Low Back Pain Taking WHO Step III Analgesics But Showing a Lack of Tolerability
• Safety Study of HZT-501 in Patients Who Require Long-Term Daily Non-steroidal Anti-inflammatory Drug Treatment
• A Pilot Study of Ultra Rapid Opioid Rotation and Titration of Oxymorphone
• Double-Blind Follow-on Safety Study of HZT-501 (Ibuprofen 800 mg/Famotidine 26.6 mg) in Subjects Who Have Completed Participation in HZ-CA-301 (NCT00450658) or HZ-CA-303 (NCT00450216)