Clinical Trials Logo

Postoperative Pain clinical trials

View clinical trials related to Postoperative Pain.

Filter by:

NCT ID: NCT02284620 Recruiting - Postoperative Pain Clinical Trials

Continuous Femoral Nerve Block Versus Local-wound Infiltration Analgesia For Patients Receiving Total Knee Arthroplasty --- A Randomized Controlled Trial

Start date: January 2015
Phase: Phase 4
Study type: Interventional

Post-operative pain after total knee arthroplasty is usually severe and impair the functional recovery of operated joints.The purpose of this study is to determine whether post-operative continuous femoral nerve block analgesia is superior to local wound infiltration combined with intravenous patient controlled analgesia in improving joint function and reducing the incidence of chronic post-surgical pain (CPSP).

NCT ID: NCT02279628 Recruiting - Postoperative Pain Clinical Trials

Continuous Pre-uterine Wound Infiltration Versus Intrathecal Morphine for Postoperative Analgesia After Cesarean Section

Start date: July 2014
Phase: Phase 4
Study type: Interventional

The cesarean section is considered as a painful surgery during the post operative period. Mothers may need to move immediately after the surgery to take care of their babies. This may increase the risk of major pain and chronic pain. Thus, excellent postoperative analgesia is required so that mothers do not experience pain in caring for their baby. Currently, several techniques have been developed to manage postoperative pain related to c-section scar such as intrathecal morphine during spinal anesthesia or continuous pre-peritoneal wound infiltration. The comparison between anesthetic techniques has never been performed and it is still not know if the combination of intrathecal morphine plus continuous pre-peritoneal wound infiltration provide a synergistic or additional effect on pain relief.

NCT ID: NCT02263963 Completed - Postoperative Pain Clinical Trials

The Transversus Abdominis Plane Block: A Prospective Randomized Clinical Trial Using EXPAREL.

Start date: July 2013
Phase: Phase 4
Study type: Interventional

The purpose of the study is to evaluate the effectiveness of EXPAREL in a transversus abdominis plane block by assessing the demand of postoperative narcotic, length of hospital stay and incidence of postoperative complications.

NCT ID: NCT02255955 Not yet recruiting - Postoperative Pain Clinical Trials

Postoperative Analgesia in Laminectomy

(PAL)
Start date: October 2014
Phase: Phase 4
Study type: Interventional

Compare the analgesic effects of naproxen sodium codeine, paracetamol codeine and placebo on postoperative pain and tramadol (Contramal) consumption during the first 24 hour after a lumbar disk surgery.

NCT ID: NCT02254525 Terminated - Postoperative Pain Clinical Trials

A Multicenter Trial of the Efficacy and Safety of a New Formulation of Ibuprofen 800 mg Every 6 Hours in the Management of Postoperative Pain

Start date: May 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to study the efficacy of intravenous administration of ibuprofen compared to placebo in patients with postoperative pain and evaluate its tolerability and safety profile.

NCT ID: NCT02235506 Recruiting - Postoperative Pain Clinical Trials

A Comparison of Epidural Block With Adding Sciatic Block to Continuous Femoral Block in Total Knee Arthroplasty

Start date: September 2014
Phase: N/A
Study type: Interventional

The investigators compared continuous epidural infusion with combined continuous femoral and single-shot sciatic nerve blocks. The primary outcome was the incidence of side effects, and secondary outcomes were pain relief, motor blockade,morphine consumption, and rehabilitation indices.

NCT ID: NCT02230865 Recruiting - Postoperative Pain Clinical Trials

Prediction of Acute Postoperative Pain and Analgesic Consumption

MIRPEX-3
Start date: August 2014
Phase: N/A
Study type: Observational

Pain is an expected part of surgical recovery but effective pain management remains challenging. The high variability in postoperative pain experience and analgesic treatment response between patients is part of the challenge. Few studies have yet combined preoperative assessment of responses to experimental pain with measurements of cognitive and emotional processes in the prediction of postoperative pain. We hypothesize, that preoperative evoked brain potentials (using standard electroencephalographic brain imaging), endogenous pain inhibition capacity (conditioned pain modulation), responses to pressure/thermal pain stimulation, and/or situational pain-related catastrophic thinking are useful clinical predictors of postoperative pain and analgesic consumption.

NCT ID: NCT02219581 Terminated - Postoperative Pain Clinical Trials

Steroids in Total Knee Arthroplasty

Start date: October 16, 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate if the use of two small doses of intravenous (IV) steroids around the time of knee replacement surgery decrease a patient's pain or use of pain medication. The investigators will also determine if the subjects receiving the steroid will have better pain control and better postoperative outcomes after their surgery.

NCT ID: NCT02216682 Not yet recruiting - Postoperative Pain Clinical Trials

Assessing the Efficacy of Intravenous Acetaminophen Versus the Oral Formulation for Perioperative Pain Treatment

Start date: August 2014
Phase: N/A
Study type: Observational

To compare oral (PO) to intravenous (IV) acetaminophen with postoperative pain scores, and consumptions of opiates, among orthopedic surgery patients undergoing total knee replacement with spinal anesthesia. Our hypothesis is that IV acetaminophen patients will have improved analgesia, less opioid consumption, a lower percentage of patients rescuing, or a longer time to first rescue with IV acetaminophen. The investigators will compare the efficacies of oral and intravenous acetaminophen for postoperative pain control, and utilization of opiates as rescue agents.

NCT ID: NCT02209233 Withdrawn - Anxiety Clinical Trials

Effects of Massage on Post-operative Pain in Urologic Patients

Start date: February 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect that receiving massage therapy post-operatively has on reducing perceived anxiety and pain in urology patients. Secondarily, the result of massage on patient satisfaction, length of hospital stay, and narcotic use will also be studied.