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Postoperative Pain clinical trials

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NCT ID: NCT02305719 Recruiting - Postoperative Pain Clinical Trials

Regional Anesthesia for Thoracoscopic Surgery

RATS
Start date: July 2014
Phase: N/A
Study type: Observational [Patient Registry]

Aim of the study is to evaluate different regional anesthesia regimes for thoracoscopic surgery to evaluate their efficiency in (postoperative) pain control. Three regional anesthesia forms are evaluated: thoracic epidural anesthesia, (ultrasound-guided) serratus-anterior-plane-block an local infiltration with local anesthetic at the site of performing the thoracoscopy.

NCT ID: NCT02287246 Recruiting - Postoperative Pain Clinical Trials

Efficacy of Extended-Release Liposomal Bupivacaine for Post-Operative Urogynecologic Surgery

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

To study post-operative efficacy of Exparel® for pain control in patients undergoing any Urogynecology surgery involving the posterior vaginal wall using a randomized, double-blinded placebo controlled trial.

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: 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: NCT02160236 Recruiting - Postoperative Pain Clinical Trials

Comparison of Postoperative Analgesic Efficacy of Intravenous Dexketoprofen Trometamol With Tenoxicam

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

In this study the investigators aimed to compare of postoperative analgesic effects of intravenous dexketoprofen trometamol and tenoxicam in lumbar disc surgery.

NCT ID: NCT02150239 Recruiting - Postoperative Pain Clinical Trials

A Survey on Postoperative Pain (POP) Experience in Asian Patients.

Start date: May 2014
Phase: N/A
Study type: Observational [Patient Registry]

Pain management is becoming an important ethical responsibility of the medical profession and a focus of the health care system. However, there are limited literature evaluate the postoperative pain experience and management in our local setting.

NCT ID: NCT02130544 Recruiting - Postoperative Pain Clinical Trials

Acute Pain Management Following Video-assisted Thoracoscopic Surgery: Comparison of Lobectomy and Wedge Resection

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

Viedo-assisted thoracoscopic surgery(VATS) have became popular in recent years. There is no golden rule of postoperative analgesia for VATS. Compared with lobectomy, wedge resection preserves better pulmonary function and is suitable for elder patients and patients who could not afford to have lobectomy. In addition to surgery time态recovery time and hospital stay, wound incisions and organization damages are different,too. Will patients also have different response to pain control after these two surgery? The retrospective study is to compared the differences of postoperative pain management between VATS lobectomy and wedge resection.

NCT ID: NCT02104778 Recruiting - Postoperative Pain Clinical Trials

Effect of Dexamethasone and Epinephrine on the Duration of Sciatic Nerve Blocks With Ropivacaine

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

The aim of the present study is to test that adding dexamethasone or epinephrine significantly prolongs the duration of sciatic nerve blocks with ropivacaine and that the magnitude of the effect differs among dexamethasone and epinehrine.