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Pain, Postoperative clinical trials

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NCT ID: NCT03434275 Completed - Pain, Postoperative Clinical Trials

Evaluation of Preoperative N1539 in Total Knee Arthroplasty

Start date: February 19, 2018
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to assess the effect of preoperative administration of N1539 on opioid consumption in subjects undergoing open unilateral total knee arthroplasty compared to placebo.

NCT ID: NCT03429400 Completed - Pain, Postoperative Clinical Trials

Study of Oral Morphine Sulfate Administration in Pediatric Subjects

Start date: April 17, 2018
Phase: Phase 3
Study type: Interventional

This is a multicenter, open-label study to evaluate the safety and PK of oral morphine sulfate in pediatric subjects with post-operative pain.

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: NCT03428230 Completed - Pain, Postoperative Clinical Trials

Intrathecal Paracetamol Before Spinal Anaesthesia With Chloroprocaine HCl 1% for Short Knee Procedures

Start date: August 6, 2018
Phase: Phase 2
Study type: Interventional

This is a phase II, single centre, randomised, parallel-group, double-blind, three doses, placebo-controlled, exploratory efficacy and safety study. The objective of this study is to investigate the efficacy and safety of a single intrathecal injection of Paracetamol 3% (30 mg/mL) administered at 3 doses to 3 active treatment groups, as compared to placebo, for post-operative analgesia in knee procedures up to 40 min duration performed under spinal anaesthesia with Chloroprocaine HCl 1%.

NCT ID: NCT03428152 Completed - Pain, Postoperative Clinical Trials

Superior Hypogastric Blockade for Postoperative Pain

Start date: February 9, 2018
Phase:
Study type: Observational [Patient Registry]

The primary indication for superior hypogastric (SHP) block is visceral pelvic pain, most commonly from malignancy of the ovary, uterus, cervix, bladder, rectum or prostate. Percutaneous SHP blocks should be done under guidance of ultrasonography, fluoroscopy, magnetic resonance or computed tomography. Because of the close proximity of SHP to major vessels, and structures like vertebral column (for posterior) and guts (for anterior) are being on the way of the needle, these percutaneous blocks are associated with serious complications. Performing SHP during hysterectomy surgery, gives advantages to rule out these complications by exploring the whole intraabdominal anatomy. The investigators' theory is to find out if SHP blocks (during pelvic surgery) are useful for decreasing VAS pain scores and opioid consumption for postoperative pain.

NCT ID: NCT03427840 Recruiting - Pain, Postoperative Clinical Trials

Superior Hypogastric Plexus Blockade in Laparoscopic Hysterectomy

Start date: March 18, 2018
Phase:
Study type: Observational

The primary indication for superior hypogastric plexus (SHP) block is visceral pelvic pain, most commonly from malignancy of the ovary, uterus, cervix, bladder, rectum or prostate. Per-cutaneous SHP blocks should be done under guidance of ultrasonography, fluoroscopy, magnetic resonance or computed tomography. During minimally invasive laparoscopic surgery, percutaneous technique can be done under the guidance of cameras.

NCT ID: NCT03425162 Completed - Postoperative Pain Clinical Trials

Ultrasound Guided Anterior Quadratus Lumborum Block

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

Percutaneous nephrolithotomy (PNL) is frequently used today for renal stones. percutaneous nephrolithotomy (PNL) procedure has become the treatment of choice for many patients with symptomatic renal stones . Patients undergoing PNL suffer from acute postoperative pain, despite a multimodal analgesic regime. This is a randomised controlled trial efficacy of the anterior Quadratus Lumborum Block (QLB) in terms of analgesic efficacy in patients who undergo percutaneous nephrolithotomy.

NCT ID: NCT03422783 Recruiting - Anesthesia Clinical Trials

Correlation Between NOL Index After Stimulus and Post-operative Opioid, Pain, Pre-operative Phenotype

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

This study evaluates the correlation between NoL index response to standardized stimulus under general anesthesia and the post-operative pain, assessed by opioid consumption and numerical pain scores after video-assisted thoracoscopy (VATS).

NCT ID: NCT03421821 Completed - Postoperative Pain Clinical Trials

The Difference Between the Extrafascial Injection and the Subfascial Injection of Quadratus Lumborum Block

Start date: February 25, 2018
Phase: N/A
Study type: Interventional

Quadratus lumborum block can be used for the hip surgery and abdominal surgery postoperative analgesia. But the lower thoracic to the hip dermatome can't be blocked at the same time. The anesthetists used the same method, but had produced the different dermatome were blocked. The investigators hypothesized that this was due to local anesthetics was injected to different locations of the anterior thoracolumbar fascia. If the investigators inject local anesthetics to the anterior layer of thoracolumbar extrafascial, this produced the dermatomal coverage from lower abdominal to hip. A different situation was when the investigators injected local anesthetics to anterior thoracolumbar subfascia, the lower thoracic dermatome were blocked.

NCT ID: NCT03420703 Completed - Postoperative Pain Clinical Trials

Erector Spinae Plane Block for Postoperative Analgesia for Laparoscopic Cholecystectomy

Start date: February 24, 2018
Phase: N/A
Study type: Interventional

Erector Spinae Plane Block is a newly defined regional anesthesia technique. Its use for many indications has been identified by case reports in the literature. As the investigators have considered that erector spinae plane block could be efficacious for providing postoperative analgesia in laparoscopic cholecystectomy, the investigators have implemented application of this blockade into practice at the clinic. Main purpose of this study is to evaluate the analgesic effect of ultrasound guided erector spinae block in laparoscopic cholecystectomy.