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Post-operative Pain clinical trials

View clinical trials related to Post-operative Pain.

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NCT ID: NCT02751346 Completed - Pain Clinical Trials

Persistent Pain After Cystectomy for Bladder Cancer

Start date: January 2016
Phase:
Study type: Observational

This single-center, cross-sectional survey and sensory examination is conducted to determine the prevalence, sensory characteristics and risk factors of PPSP in patients who underwent cystectomy at Washington University/Barnes-Jewish Hospital between 2009 and 2015. Based on data from other lower abdominal surgeries, the investigators hypothesize that 10-15% of patients undergoing cystectomy will develop PPSP.

NCT ID: NCT02741492 Completed - Post-Operative Pain Clinical Trials

Transversus Abdominus Plane Catheters for Open Inguinal Hernia Repair

Start date: April 2016
Phase: N/A
Study type: Interventional

This study is designed to evaluate pain control of continuous transversus abdominis plane (TAP) blocks placed for open inguinal hernia repair. The investigators hypothesize that there will be improved pain control when compared with sham blocks.

NCT ID: NCT02737124 Withdrawn - Post Operative Pain Clinical Trials

Acetaminophen Randomized Controlled Trial

Start date: February 16, 2017
Phase: Phase 3
Study type: Interventional

Patients that are to undergo isolated meniscectomy will be randomized to 2 cohorts: one will take the FDA recommended dose of acetominophen (1000mg) 24hrs before surgery, one will be given a similarly looking placebo pill. A multitude of post-op variables will be included, mainly pain scores and morphine equivalent doses at different time points.

NCT ID: NCT02711501 Completed - Post-operative Pain Clinical Trials

Comparison of Post-operative Complications of Bone Augmentation at Anterior of Maxilla After Periosteal Releasing Incision With Two Techniques Diode Laser and Scalpel

Start date: March 2016
Phase: N/A
Study type: Interventional

The aim of this study was to investigate if using lasers instead of scalpel for flap advancement in bone augmentation procedures would reduce post-operative swelling and pain.

NCT ID: NCT02701114 Completed - Post-Operative Pain Clinical Trials

Proximal Versus Distal Adductor Canal Blocks for Total Knee Arthroplasty

Start date: February 2016
Phase: N/A
Study type: Interventional

This study is designed to evaluate pain control of continuous adductor canal blocks placed proximally versus distally within the canal. The investigators hypothesize that there will be similar pain control between both groups.

NCT ID: NCT02689063 Completed - Post Operative Pain Clinical Trials

Maxigesic IV Phase 3 Bunionectomy Study

Start date: October 26, 2016
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the clinical efficacy and safety of Maxigesic IV, acetaminophen IV, Ibuprofen IV versus placebo IV for the treatment of acute postoperative pain after bunionectomy

NCT ID: NCT02689011 Completed - Acute Pain Clinical Trials

Incidence of Urinary Retention in Patients Undergoing Unilateral Total Knee Arthroplasty- Comparison Between Continuous Epidural Analgesia and Single Shot Femoral Nerve Block- a Randomized Controlled Study (UriKANE)

UriKANE
Start date: January 2014
Phase: N/A
Study type: Interventional

This study aims to compare the incidence of urinary retention and requirement of bladder catheterization in patients undergoing total knee arthroplasty while receiving either continuous epidural analgesia or single shot femoral nerve block.

NCT ID: NCT02687451 Terminated - Acute Pain Clinical Trials

Clinical Study to Evaluate the Effectiveness, Safety, and Tolerability of Oxymorphone Immediate Release (IR) Oral Liquid in Post Surgical Pediatric Subjects

Start date: April 2016
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy, tolerability, safety and pharmacokinetics of Oxymorphone HCl as an analgesic for acute moderate to severe post-operative pain in pediatric subjects.

NCT ID: NCT02651324 Active, not recruiting - Post-operative Pain Clinical Trials

Efficacy of Ketamine for Improvement in Postoperative Pain Control After Spinal Fusion for Idiopathic Scoliosis

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

This study hypothesizes that the addition of a low-dose ketamine infusion to usual post-operative pain management will improve pain control as evidenced by an improvement in post-operative pain scores for patients undergoing spinal fusion for idiopathic scoliosis.

NCT ID: NCT02577809 Completed - Post-operative Pain Clinical Trials

Intrathecal Opioid Study

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

This is an interventional drug trail to evaluate the effect of different intrathecal opioids on post-operative pain experiences in women who have undergone caesarean section surgery.