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Pain, Postoperative clinical trials

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NCT ID: NCT03435692 Terminated - Hip Surgery Clinical Trials

Post Operative Pain Control After Pediatric Hip Surgery

Start date: July 15, 2011
Phase: N/A
Study type: Interventional

Hip surgery in children is painful and the optimal modality for managing post-operative pain has not been established. This prospective randomized controlled trail compares lumbar plexus catheter (LPC), lumbar epidural catheter (LEC) and continuous patient-controlled analgesia (PCA) with intravenous morphine.

NCT ID: NCT03434847 Terminated - Pain, Postoperative Clinical Trials

Providing Patients Realistic Expectations of Postoperative Pain

PPREOPP
Start date: October 21, 2017
Phase: N/A
Study type: Interventional

Prospective, randomized, single-blind study, whether perioperative educational improves pain-related postoperative outcomes,

NCT ID: NCT03428984 Terminated - Clinical trials for Postoperative Pain Management

Study in Adult Subjects Undergoing Posterolateral Thoracotomy

Start date: May 3, 2018
Phase: Phase 1
Study type: Interventional

Primary Objective: To characterize the pharmacokinetic (PK) profile of EXPAREL when administered as a posterior intercostal nerve block. Secondary Objective: To assess the safety and tolerability of EXPAREL in this surgical model.

NCT ID: NCT03383198 Terminated - Pain, Postoperative Clinical Trials

Pectoralis (II) Block With Liposomal Bupivacaine vs Bupivacaine for Breast Surgery

Start date: December 1, 2017
Phase: Phase 4
Study type: Interventional

This is a randomized controlled pilot study evaluating length of pain control with either liposomal bupivacaine or with bupivacaine plus decadron after PEC II injection in patients having bilateral mastectomies with immediate reconstruction.

NCT ID: NCT03316118 Terminated - Postoperative Pain Clinical Trials

US Guided GNB vs Saline Injection for TKA

Start date: October 5, 2017
Phase: Phase 4
Study type: Interventional

Do ultrasound-guided genicular nerve blocks with 0.5% bupivacaine provide improved knee analgesia for patients recovering from total knee replacement surgery compared to saline injection? Hypotheses: The investigators hypothesize that the combination of ultrasound-guided adductor canal block (ACB) and genicular nerve block will achieve lower opioid consumption and therefore lead to decreased systemic side effects and improved overall satisfaction compared to ultrasound-guided saline injection for patients undergoing minimally invasive elective total knee arthroplasty (TKA).

NCT ID: NCT03268278 Terminated - Postoperative Pain Clinical Trials

Efficacy of Buprenorphine on Postoperative Endodontic Analgesia

EBPEA
Start date: April 1, 2017
Phase: Phase 1
Study type: Interventional

To see whether the addition of buprenorphone to local anesthesia will lengthen postoperative analgesia for endodontic pain

NCT ID: NCT03265249 Terminated - Pain, Postoperative Clinical Trials

BRIDGE Device for Post-operative Pain Control

BRIDGE
Start date: February 12, 2018
Phase: N/A
Study type: Interventional

Auricular neurostimulation is a potential novel and non-invasive method of pain control following liver transplantation in a growing patient population with the probability of significant impact on economics and morbidity. The investigators propose a pilot study to investigate the effects of auricular neurostimulation in patients receiving a liver transplantation. The investigator will investigate the effects of auricular neurostimulation with this novel device and compare it to the current standard of care for pain management following liver transplantation.

NCT ID: NCT03261193 Terminated - Pain, Postoperative Clinical Trials

ITM + Bupivacaine QLB vs. ITM + Sham Saline QLB for Cesarean Delivery Pain

qlcsection
Start date: September 5, 2017
Phase: Phase 3
Study type: Interventional

Comparison of standard post-operative cesarean surgery pain management with regional post-op pain control.

NCT ID: NCT03253224 Terminated - Dexmedetomidine Clinical Trials

Magnesium and Postoperative Pain

Start date: September 10, 2017
Phase: Phase 4
Study type: Interventional

With ongoing advancements in healthcare leading to prolonged life expectancy, orthopedic surgeries are increasingly performed in elderly patients. Total knee arthroplasty, in particular, has been increasing with the growing demand for improved mobility and quality of life. Total knee arthroplasty is performed on patients with advanced and painful osteoarthritis of the knees, but it can result in moderate to severe postoperative pain during the recovery period. To relieve anxiety or stress during surgery under regional anesthesia, sedation can be provided. Dexmedetomidine is a sedative-analgesic agent acting as α2-adrenergic receptor agonist, and its analgesic effect has been well established in various procedures or surgeries. Magnesium has been reported to produce important analgesic effects including the suppression of neuropathic pain, potentiation of morphine analgesia, and attenuation of morphine tolerance. Although the exact mechanism is not yet fully understood, the analgesic properties of magnesium are believed to stem from regulation of calcium influx into the cell and antagonism of N-methyl-D-aspartate (NMDA) receptors in the central nervous system. In this study, investigators will evaluate the reducing effect of magnesium on the post-total knee arthroplasty pain in patients sedated with dexmedetomidine under spinal anesthesia.

NCT ID: NCT03206008 Terminated - Postoperative Pain Clinical Trials

The Effect of Intraoperative Magnesium Sulfate Infusion on the Postoperative Recovery

Start date: November 18, 2016
Phase: N/A
Study type: Interventional

Evaluating analgesic effect of intraoperative magnesium sulfate infusion in the outpatient surgery case