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Pain, Postoperative clinical trials

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NCT ID: NCT04560712 Active, not recruiting - Clinical trials for Resectable Pancreatic Carcinoma

Acupuncture for the Management of Postoperative Pain in Patients With Pancreatic or Colorectal Cancer Undergoing Surgery

Start date: August 12, 2020
Phase: N/A
Study type: Interventional

This trial investigates how well acupuncture works for the management of pain after surgery in patients having open colorectal or pancreatic surgery. Acupuncture may help to reduce postoperative symptoms including pain. This study may help researchers learn if acupuncture reduces after-surgery side effects and improves recovery.

NCT ID: NCT04533009 Active, not recruiting - Pain, Postoperative Clinical Trials

Tramadol-paracetamol Combination in Treatment of Patients Undergoing Spinal Surgery

TRAMAPARAS
Start date: February 1, 2020
Phase: Phase 4
Study type: Interventional

Tramadol-paracetamol combination is studied in patients coming for elective spine surgery. The study drug is started at the day of surgery and continued maximum of five days. Before the surgery pain, use of pain medication, satisfaction for pain medication, adverse effects, resilience, depression and life satisfaction were asked. At the discharge and seven days after the surgery use of pain medication and adverse effects were asked. The patients were followed up to 28 days and one year after surgery.

NCT ID: NCT04488315 Active, not recruiting - Pain, Postoperative Clinical Trials

Scalp Infiltration With Dexamethasone Plus Ropivacaine for Post-craniotomy Pain

Start date: October 1, 2022
Phase: Phase 4
Study type: Interventional

According to recent studies, patients following craniotomy suffer more than minimal pain; two-thirds of patients experienced moderate to severe pain. Postoperative pain most often occurs within 48 hours after surgery. Local infiltration of anesthesia is the most simple and effective analgesia. However, the analgesic effect only lasts for a short-time after surgery, and it cannot adequately meet the needs of postoperative analgesia after craniotomy. Several studies have shown that the mixture of dexamethasone with local anesthetics could reduce the postoperative pain scores better than local anesthetics alone. Lipid microsphere is a relatively new drug delivery system. It is an artificial lipid emulsion. Studies have shown that dexamethasone lipid microsphere, the dexamethasone palmitate emulsion (D-PAL emulsion), has stronger anti-inflammatory effect than dexamethasone. Therefore, the investigators hypothesize that the pre-emptive scalp infiltration with dexamethasone lipid microsphere plus ropivacaine could achieve superior postoperative pain-relief compared to ropivacaine alone for patients undergoing craniotomy.

NCT ID: NCT04481451 Active, not recruiting - Pain, Postoperative Clinical Trials

Quadratus Lumborum vs Erector Spinae Supplementary Blocks With Lumbar Plexus Blocks for Hip PAO

Start date: December 1, 2020
Phase: Phase 4
Study type: Interventional

This study proposes to evaluate the efficacy of single shot erector spinae block (ESB) versus single shot quadratus lumborum block (QLB) when used in conjunction with continuous lumbar plexus block (LPB) for postoperative analgesia in children and adolescents undergoing unilateral hip surgical procedures. The aim of this study is to compare the efficacy of the QL vs. ESP blocks as supplements to the lumbar plexus block with respect to pain control outcomes after hip PAO surgery. Both blocks are safe and easy to perform. There is currently no comparative, prospective data concerning the use of these two blocks for hip surgery. The investigational hypothesis is that there will be no clinical difference in the amount of opioid consumed or the overall pain control offered by these two block options.

NCT ID: NCT04474873 Active, not recruiting - Postoperative Pain Clinical Trials

Effectivenes of Erector Spinae Plane Block in Percutaneous Nephrolithotomy?

Start date: March 1, 2020
Phase: N/A
Study type: Interventional

This study investigates the effectiveness of the erector spinae plane block (ESPB) in pain management of patients undergoing PNL.

NCT ID: NCT04437888 Active, not recruiting - Pain, Postoperative Clinical Trials

Intraoperative Ketamine for Patients Undergoing Total Joint Arthroplasty

Start date: September 14, 2020
Phase: Early Phase 1
Study type: Interventional

Prospective randomized double blinded, placebo controlled study that will evaluate the effect of intra-operative ketamine administration on post-operative analgesic requirements and self-reported pain in patients undergoing total hip and total knee arthroplasty who demonstrate high levels of pain catastrophizing.

NCT ID: NCT04382209 Active, not recruiting - Postoperative Pain Clinical Trials

The Goal of This Study is to Evaluate the Effect of Ultrasound Guided Erector Spinae Plane Block on Postoperative Pain After Major Abdominal Surgeries

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

Aim of the work To evaluate the efficacy of ultrasound-guided erector spinae plane block for management of postoperative pain in patients undergoing major abdominal surgery under general anesthesia. Hypothesis - Null hypothesis: The investigators suppose that ultrasound-guided erector spinae plane block has no post-operative analgesic effect in patients undergoing major abdominal surgery. - Alternative hypothesis: The investigators suppose that ultrasound-guided erector spinae plane block has post-operative analgesic effect in patients undergoing major abdominal surgery. Study objectives Primary Objective: Comparison of opioid consumption in patients receiving erector spinae plane block in relation to control group. Secondary Objective: 1. Evaluate the hemodynamics (blood pressure, heart rate) and respiratory rate in patients receiving erector spinae plane block during postoperative period at 0, 2, 4, 6, 8, 12,24 hours. 2. Assessment of numeric rating scale (NRS) in patients receiving erector spinae plane block during rest and movement during postoperative period at 0, 2, 4, 6, 8, 12,24 hours.

NCT ID: NCT04365088 Active, not recruiting - Clinical trials for Impacted Third Molar Tooth

Evaluation of the Effects of Pre-operative Deflazacort on Post-operative Pain, Edema and Trismus

Start date: December 15, 2018
Phase: Phase 4
Study type: Interventional

Removal of impacted lower third molar teeth is one of the most common oral surgical procedures, and these operations often lead to various complications in patients. Antibiotics, analgesics and/or anti-inflammatory drugs are prescribed for the treatment of complications encountered. Anti-inflammatory is the property of a substance or treatment that reduces inflammation or swelling. Anti-inflammatory drugs make up about half of analgesics, remedying pain by reducing inflammation as opposed to opioids, which affect the central nervous system to block pain signaling to the brain. Based on this information, in this study, it is aimed to evaluate the effects of deflazacort preoperatively on the postoperative pain, swelling and trismus.

NCT ID: NCT04349397 Active, not recruiting - Pain, Postoperative Clinical Trials

Use of Analgesics and Pain Scores After Pediatric Adenotonsillectomy

Start date: August 1, 2019
Phase:
Study type: Observational

The purpose of the study is to quantify the use of pain medications given to children aged 3 - 12 years as well as their pain level through pain scores after they have undergone a tonsillectomy or adenotonsillectomy surgery at Doernbecher Children's Hospital (DCH). We would like to learn more about the pain medications given and the pain scores of children post-surgery for the first 5 days following discharge from the hospital.

NCT ID: NCT04341948 Active, not recruiting - Postoperative Pain Clinical Trials

Treatment of Post-Operative Pain Following Orthopedic Surgery With SPRINT® Peripheral Nerve Stimulation (PNS) System

Start date: August 6, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to gather information about how knee pain changes when small amounts of electricity are delivered to the nerves in the leg. This study will involve the use of a Peripheral Nerve Stimulation (PNS) System that is made by SPR Therapeutics (the sponsor of the study). The SPRINT PNS System was cleared by the FDA for up to 60 days of use in the back and/or extremities for the management of acute and chronic pain.