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Pain, Postoperative clinical trials

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NCT ID: NCT02737124 Withdrawn - Post Operative Pain Clinical Trials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: NCT02732262 Completed - Pain Clinical Trials

Optimal Dose of i.v Oxycodone for Postoperative Pain

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

Postoperative pain control is required after major abdominal surgery, including laparoscopic colorectal surgery. Intravenous oxycodone is widely used for postoperative acute pain control mainly in Europe. The aim of this study is to evaluate the optimal dose of intravenous oxycodone for pain control after laparoscopic colorectal surgery in Korean.

NCT ID: NCT02731950 Completed - Pain Clinical Trials

Presternal Bupivacaine Plus Magnesium Sulfate Infusion After Cardiac Surgery

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

Effective pain relief after cardiac surgery has assumed importance with the introduction of fast track discharge protocols that requires early weaning from mechanical ventilation. Inadequate pain control reduces the capacity to cough, mobility, increases the frequency of atelectasis, and prolongs recovery. Infiltration of local anesthetics near the surgical wound has shown to improve early postoperative pain in various surgical procedures. Magnesium is the fourth most plentiful cation in our body. It has antinociceptive effects in animal and human models of pain.

NCT ID: NCT02731430 Active, not recruiting - Postoperative Pain Clinical Trials

Intrathecal Morphine for Postoperative Analgesia Following Laparoscopic Bariatric Surgery

Start date: December 2015
Phase: Phase 2/Phase 3
Study type: Interventional

this study compares the use of intrathecal morphine, to multimodal analgesic techniques for postoperative pain management following laparoscopic bariatric surgery.

NCT ID: NCT02730728 Completed - Osteoarthritis Clinical Trials

Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA

Start date: November 1, 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to compare a single shot block, 24 hours, and 48 hour continuous catheter nerve block done via the adductor canal method in adult patients who have under gone total knee arthroplasty. Visual analogue scores, opioid consumption, time to up and go, ambulation, manual muscle tests, and Tinetti scores up to 72 hours post operatively will be used for comparison.

NCT ID: NCT02729935 Completed - Postoperative Pain Clinical Trials

Parecoxib for Treatment of Catheter Related Bladder Discomfort

Start date: March 2016
Phase: Phase 4
Study type: Interventional

Catheter-related bladder discomfort (CRBD) is defined as an urge to void or discomfort in the supra-pubic region; reported postoperatively in patients who have had urinary catheterization intra-operatively. In the present study, the investigators evaluated Parecoxib (P) for preventing CRBD in patients undergoing catheterization after transurethral resection of bladder tumor (TURBT).

NCT ID: NCT02728323 Terminated - Pain Clinical Trials

Transversus Abdominis Plane Block in the Management of Acute Postoperative Pain Syndrome After Caesarean Section

Start date: October 2013
Phase: Phase 3
Study type: Interventional

In many countries, caesarean section (CS) rates have been increasing. The international literature is unclear regarding the analgesic efficacy of the transversus abdominis plane block (TAPB) after a CS. In particular, no clinical trials exist in which the correct method of performing this block has been matched with the obtained analgesic effect after a CS. The primary goal of the study was to determine whether a correctly performed ultrasound-guided TAPB (USG-TAPB) could provide patients who underwent a CS with better control of acute postoperative pain during the first 72 hours after surgery

NCT ID: NCT02728310 Terminated - Pain Clinical Trials

Local Continuous Wound Infusion of Anesthetics in the Management of Post-operative Pain After Total Hip Arthroplasty.

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

The combination of subarachnoid anaesthesia (SAB) and continuous local wound infiltration (LCWI) with a consistent amount of local anaesthetics could prevent central sensitization through an additive or synergistic effect because it can maintain continuous inhibition of nociceptive afferents

NCT ID: NCT02727491 Completed - Pain, Postoperative Clinical Trials

Does Pre and Postoperative Dextromethorphan Reduce Post-tonsillectomy Pain in Children?

Start date: March 2012
Phase: Phase 4
Study type: Interventional

With Institutional ethics board and Health Canada approval, pediatric patients (ages 3-12) undergoing tonsillectomy or adenotonsillectomy (under standardized anesthesia) will be randomized to receive dextromethorphan hydrobromide (1mg/kg orally) 30 min preoperatively and again 8 hours postoperatively OR placebo (syrup identical in taste, appearance and volume) at the same time points. The primary outcome is an integrated assessment of perioperative pain scores and opioid use for 24 hours postoperatively. Secondary outcomes include nausea, vomiting, respiratory depression, and bleeding for 24 hours postoperatively. Our hypothesis is that dextromethorphan will decrease the incidence/severity of post-tonsillectomy pain. The improved pain control will be apparent through reduced opioid consumption and integrated pain scores. This will result in a reduced incidence of opioid-related side effects and adverse events.

NCT ID: NCT02726828 Completed - Postoperative Pain Clinical Trials

intrathecaم Ketamine, Morphine and Both for Lower Abdominal Cancer Surgery Pain

Start date: October 2015
Phase: Phase 2/Phase 3
Study type: Interventional

this study investigates the analgesic efficacy and other possible effects of ketamine, morphine, and both together when administered intrathecally for control of postoperative pain following lower abdominal cancer surgeries.