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Pain, Postoperative clinical trials

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NCT ID: NCT03415555 Completed - Postoperative Pain Clinical Trials

Postoperative Analgesia After Minithoracotomy

Start date: February 7, 2018
Phase: Phase 4
Study type: Interventional

Patients scheduled for minimally invasive mitral valve replacement. Each patient will be treated with intravenous (i.v.) oxycodone - patient-controlled analgesia (PCA). Half of the patients will be randomly allocated to Erector Spinae Plane (ESP) blockade group.

NCT ID: NCT03415204 Completed - Clinical trials for Arthroplasty Complications

Acupuncture for Post Operative Pain Following Total Knee or Hip Arthroplasty

Start date: December 20, 2017
Phase: N/A
Study type: Interventional

Post operative pain (POP) is a major obstacle on the road to healing, despite the increasing interest in postoperative pain management and development of pain control modalities (1). Postoperative pain is still insufficiently treated with more than 50% of patients suffering from moderate to severe pain early after surgery .Pain after orthopedic surgery is considered especially difficult to manage. Approximately half of total knee or hip arthroplasty patients present with extreme pain immediately after surgery. Total knee and hip arthroplasty often results not only in severe perioperative pain and debilitation, but chronic pain, joint stiffness, and functional disability many months or even years following the procedure. Various modalities of treating orthopedic POP exist, but the optimal management of postoperative pain remains controversial with no clear consensus of the best method.We suggest that acupuncture can be an effective treatment for post operative pain after total knee or hip arthroplasty.

NCT ID: NCT03413280 Completed - Pain, Postoperative Clinical Trials

Preemptive Analgesic Effects of Rectus Sheath Block in Laparoscopic Cholecystectomy Patients

Start date: March 28, 2017
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate the effectiveness of preemptive effect of rectus sheath block (RSB) and intercostal nerve block (ICNB) on postoperative visceral pain in laparoscopic cholecystectomy (LLC). After induction of general anesthesia, group of patient is decided randomly. In Group pre, RSB and ICNB are performed with 0.25% Ropivacaine 40ml before the operation. In Group post, RSB and ICNB are performed with 0.25% Ropivacaine 40ml after the operation. Measure the NRS and compare the rescue analgesic dose used at 0, 0.5, 1, 2, 6, 9, 18, and 24 hours after arrival at the recovery room.

NCT ID: NCT03413163 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Bilateral Erector Spinae Plane Block in Retropubic Radical Prostatectomy

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

This study will define the postoperative analgesic effect of ESP block via amount of patient-controlled analgesia (PCA) and postoperative analgesic consumption (such as routinely and rescue analgesics) and compare the control group patients with retropubic radical prostatectomy .

NCT ID: NCT03412318 Completed - Acute Pulpitis Clinical Trials

Evaluation of the Effect of Root Canal Preparation by TF and M-Pro on Post-Operative Pain After Single Visit Endodontic Treatment

Start date: October 6, 2018
Phase: N/A
Study type: Interventional

A study to comparatively evaluate the post operative pain between root canal preparation by reciprocating file (TF) and full rotation file (M-Pro) in patients with single rooted teeth with acute irreversible pulpits.

NCT ID: NCT03411343 Completed - Pain, Postoperative Clinical Trials

Interscalene Block Versus Costoclavicular Block for Shoulder Surgery

Start date: April 9, 2018
Phase: N/A
Study type: Interventional

Interscalene brachial plexus block constitutes the analgesic criterion standard for shoulder surgery. However, it is associated with a high incidence of hemidiaphragmatic paralysis (HDP) that may not be tolerated by patients with chronic pulmonary disease. This randomized controlled trial (RCT) will compare ultrasound-guided interscalene block (ISB) and costoclavicular infraclavicular block (CCICB) in patients undergoing arthroscopic shoulder surgery. The main outcome is static pain at 30 minutes after arrival in the post anesthesia care unit (PACU) as measured by a numerical rate scale (NRS) from 0 to 10. Our research hypothesis is that interscalene and costoclavicular infraclavicular blocks will result in equivalent postoperative analgesia at 30 minutes in the PACU. The equivalence margin is set at 2 points.

NCT ID: NCT03408184 Completed - Postoperative Pain Clinical Trials

Lumbar Paravertebral in Hernia Surgery

Start date: August 9, 2016
Phase: N/A
Study type: Interventional

An inguinal hernia is one of the most common disorders requiring surgical repair in pediatrics. The effective treatment of postoperative pain in infants and children is challenging. Although the use of opioid analgesics is generally safe, adverse effects occur frequently, so the use of alternative analgesic techniques when available to improve postoperative analgesia while limiting opioid-related adverse effects, that is why there is an increase in the use of regional anesthetic techniques in infants and children.

NCT ID: NCT03407612 Completed - Pain, Postoperative Clinical Trials

Outcomes of CPM Usage Following Arthroscopic Acetabular Labral Repair

Start date: February 15, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to measure whether CPM (continuous passive motion) usage improves outcomes following arthroscopic hip surgery that includes labral repair. Investigators tested the hypothesis that CPM usage reduces pain levels and pain medication use and improves function in individuals who undergo hip arthroscopy.

NCT ID: NCT03404908 Completed - Postoperative Pain Clinical Trials

TAP vs QLB in Patients After Cesarean Delivery

Start date: February 7, 2018
Phase: Phase 4
Study type: Interventional

Comparison of two types of analgesia after cesarean section All patients will be anesthetized with spinal technique. Ultrasound-guided transversus abdominis plane or quadratus lumborum block to treat postoperative pain. Postoperative pain will be measured with visual-analog scale (VAS). 1, 2, 6 months after surgery each patient will be called to assess neuropathic pain with Neuropathic Pain Symptom Inventory (NPSI).

NCT ID: NCT03404518 Completed - Pain, Postoperative Clinical Trials

Patient Narcotic Requirements After Outpatient Otolaryngology Procedures

Start date: February 21, 2018
Phase: Phase 3
Study type: Interventional

Patient's pain level and narcotic requirements will be evaluated after routine outpatient Otolaryngology procedures. This will be done by having study participants record their pain level and medication usage from home.