search

Active clinical trials for "Pain, Postoperative"

Results 1231-1240 of 3627

Effect of Intravenous Dexmedetomidine on Analgesic Duration of Infraclavicular Block

Postoperative Pain

The study will evaluate the effect of Dexmedetomidine sedation on the duration of infraclavicular block in patients scheduled for surgery of elbow, forearm and/or hand. All patients will receive infraclavicular block before the surgery and then they will be randomized to receive either Dexmedetomidine or Propofol sedation. Duration of the sensory block will be evaluated in recovery room, 24 and 48 hours after the surgery. Hypothesis: Primary: Dexmedetomidine sedation increases the duration of sensory infraclavicular block in patients scheduled for upper limb surgery. Secondary: Dexmedetomidine sedation Gives an adequate level of sedation during the surgical procedure Reduces the requirements of postoperative opioids Improves the quality of sleep on the night of the surgery Increases patients satisfaction regarding the anesthesia technique Dexmedetomidine sedation is safe and easy to use Dexmedetomidine sedation provides less respiratory depression during the procedure.

Completed13 enrollment criteria

Pragmatic Research eXamining Inpatient Symptoms

Postoperative PainNausea3 more

Many hospitalized patients experience pain during their hospital stay, and less than half report adequate pain relief. Common treatments for pain include opioid medications, which have associated side effects and complications. Research has shown that acupuncture is effective for surgical, postoperative and cancer-related pain, nausea, and vomiting. More research is needed on the effectiveness of adding acupuncture to routine care for hospitalized patients. The objective of this study is to examine the effectiveness of acupuncture delivered in a "real-world" setting according to the principles of traditional Chinese medicine among hospitalized patients to manage pain and other symptoms. 250 hospitalized participants will be randomized in a 1 to 1 ratio to receive either 1) usual care or 2) usual care with acupuncture offered (125 in each group). The primary outcome measure will be change in daily pain intensity. Data on other symptoms, such as nausea, vomiting, anxiety, and depression, as well as functionality and quality of life will be collected in person, on a web-based survey, or via telephone follow-up. The aims of the study are to examine the effectiveness of acupuncture to manage pain and other symptoms among hospitalized patients; to evaluate the impact of acupuncture on patient satisfaction among hospitalized patients; and to estimate costs and cost-effectiveness of acupuncture among a subset of hospitalized patients. The investigators hypothesize that compared to hospitalized patients receiving usual care alone, hospitalized patients receiving acupuncture will have: decreased pain severity higher patient satisfaction

Completed7 enrollment criteria

RCT Comparing Analgesia Post-VATS With Epimorph VS Placebo

Thoracic SurgeryVideo-assisted4 more

The purpose of the study is to determine if the administration of a mix of Sufentanil and Morphine in intrathecal is a better analgesia regimen than PCA alone in patient post-VATS.

Terminated15 enrollment criteria

Effects of Local Anesthesia on Post-operative Pain During Laparoscopic Inguinal Hernia Repair

Post Operative Pain (Post Laparoscopic Hernia Repair)

To assess effect of local anesthetic into the preperitoneal space during laparoscopic hernia repair on post-operative pain.

Completed6 enrollment criteria

Analgesic Effect of Intra-articular Dexamethasone and Dexamethasone Added to Bupivacaine in Interscalene...

Postoperative Pain

the aim of this study was to investigate the analgesic efficacy of intra articular dexamethasone administration for arthroscopic shoulder surgery.

Completed9 enrollment criteria

Study to Evaluate Safety/Efficacy of a Single Pre-Op Dose of AYX1 Injection to Treat Pain After...

Postsurgical Pain

The objectives of this study are to evaluate the safety and analgesic efficacy of a single preoperative intrathecal administration of AYX1 Injection at two dose/volume levels.

Completed26 enrollment criteria

Effect of a Sciatic Block (SNB) Combined With a Continuous Femoral Block (CFNB) on Pain Scores After...

Postoperative Pain

The purpose of this study is to determine if the addition of a sciatic nerve block (SNB) to a continuous femoral nerve block (CFNB) improves post-operative analgesia after knee arthroplasty.

Completed12 enrollment criteria

Morphine Consumption in Joint Replacement Patients, With or Without Gabapentin Treatment

Post Operative PainTotal Knee Replacement

Total knee arthroplasty is amongst the most painful procedures postoperatively, and pain management can be a challenge. Different measures have been introduced to manage severe postoperative pain int hese patients. Previous studies have investigated gabapentin in acute postoperative pain and demonstrated reducted pain, postoperative morphine consumption, morphine related side effects, and postoperative pain scores. To date, this analgesia adjunct has yet to be investigated in total joint arthroplasty patients.

Completed19 enrollment criteria

Does a Single Shot Femoral Nerve Block Alone Produce Appropriate Pain Relief?

Post-operative Pain

The aim of this study is to compare the efficacy of the analgesic effect of the preoperative femoral nerve block alone versus combined femoral, sciatic, obturator and lateral femoral cutaneous nerve blocks in patients after TKA in the immediate postoperative period.

Completed9 enrollment criteria

Comparison of the Safety of Q8003 Versus Morphine Equivalent Doses of Its Components (Oxycodone...

Postoperative Pain

This is a randomized, double-blind, multicenter, repeat-dose study of fixed doses of Q8003 12 mg/8 mg given q6hr compared to morphine sulfate 24 mg and oxycodone hydrochloride 16 mg given q6hr for the management of acute moderate to severe postoperative pain for 48 hours following bunionectomy surgery.

Completed12 enrollment criteria
1...123124125...363

Need Help? Contact our team!


We'll reach out to this number within 24 hrs