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Pain, Postoperative clinical trials

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NCT ID: NCT02489851 Completed - Postoperative Pain Clinical Trials

Quadratus Lumborum Block vs Tranversus Abdominis Plane Block for Cesarean Section

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

The Quadratus Lumborum block (QLB) was first described by Blanco in 2007. The main advantage of QLB compared to the Transversus Abdominis Plane block (TAP) is the extension of local anesthetic agent beyond the TAP plane to the thoracic paravertebral space. The wider spread of the local anesthetic agents may produce extensive analgesia and prolonged action of the injected local anesthetic solution. Previous studies showed that both TAP block and QLB may reduce morphine requirements in the postoperative period in patients who had cesarean section under spinal anaesthesia. However there are no published reports comparing the 2 techniques. The aim of this randomised controlled, double blinded study is to compare the analgesic efficacy of QLB compared to TAP block in patients who had cesarean section under spinal anesthesia.

NCT ID: NCT02489526 Completed - Post-Operative Pain Clinical Trials

Evaluate the Analgesic Efficacy and Safety of VVZ-149 Injections for Post-Operative Pain Following Colorectal Surgery

Start date: September 28, 2015
Phase: Phase 2
Study type: Interventional

The purpose of this Phase 2 study is to evaluate the efficacy and safety of an analgesic drug candidate, VVZ-149 Injections. The study is designed as randomized, double-blind, parallel, placebo-controlled study.

NCT ID: NCT02487355 Recruiting - Pain, Postoperative Clinical Trials

Pediatric Caudal Dexmedetomidine Enhances Postoperative Analgesia of Magnesium Sulphate in Lower Abdominal Surgeries

JASayed
Start date: May 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The study will conduct to compare the efficacy of Magnesium sulphate & dexmedetomidine used as adjuvants to bupivacaine in caudal block to provide intra-operative anesthesia as well as post -operative analgesia in pediatric patients.

NCT ID: NCT02487303 Completed - Pain, Postoperative Clinical Trials

Intravenous Versus Oral Acetaminophen for Postoperative Pain Control After Cesarean Delivery

Start date: March 17, 2015
Phase: N/A
Study type: Interventional

This study will compare IV (intravenous) versus oral (PO) acetaminophen for postoperative pain after scheduled, elective Cesarean delivery. All patients will receive a standardized spinal anesthetic for operative anesthesia and will be randomized into one of three groups: (group 1) 1 gram IV acetaminophen every 8 hours for three doses, (group 2) 1 gram oral acetaminophen every 8 hours for three doses, or (group 3) no acetaminophen. This will be a randomized, open label study.

NCT ID: NCT02483923 Completed - Breast Cancer Clinical Trials

Analgesic Effect to Postoperative Pain After Mastectomy: Ultrasound-guided Serratus Anterior Plane Block

Start date: June 16, 2015
Phase: N/A
Study type: Interventional

Ultrasound guided serratus anterior plane block may decrease acute postoperative pain and consumption of opioid after mastectomy.

NCT ID: NCT02483689 Recruiting - Post Operative Pain Clinical Trials

Evaluation of Local Anesthetic at Incision Site

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

Patient will have usual appendectomy surgery with an injection of local or saline at incision site either before or after the incision at random. The clinical hypothesis of this trial is that pediatric patients who undergo a local anesthetic pre-incisional and/or post-incisional will reduce the amount of postoperative pain and therefore reduce the amount of analgesics required to keep the patient satisfied. Primary: To determine if local anesthetic reduces postoperative pain. Secondary: To assess the timing of local anesthetic injection affects postoperative pain.

NCT ID: NCT02483338 Recruiting - Postoperative Pain Clinical Trials

FASS (Facial Action Summary Score) Scale to Differentiate the Pain of Postoperative Anxiety in Children Under 7 Years

FASS
Start date: July 2011
Phase: N/A
Study type: Interventional

This study aims to evaluate the psychometric validity of FASS (Facial Summary Score Scale) to assess postoperative children pain.

NCT ID: NCT02483221 Completed - Clinical trials for Acute Postoperative Pain

Postoperative Pain Therapy With Hydromorphone TCI-PCA vs. Morphine PCA

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

Treatment of postoperative pain with hydromorphone (a strong analgesic) using patient-controlled analgesia with target-controlled infusion compared to conventional patient-controlled analgesia with morphine after elective cardiac surgery

NCT ID: NCT02481570 Completed - Postoperative Pain Clinical Trials

Anesthetic Optimization in Scoliosis Surgery

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

The standard anesthetic care plan for people having adolescent idiopathic scoliosis surgery will be accompanied by a pharmacokinetic simulation of the administered drugs to suggest opportunities to adjust drug doses to achieve tolerable pain control after surgery, avoid respiratory depression and allow patients to respond quickly either during intraoperative testing or at the conclusion of surgery.

NCT ID: NCT02479165 Completed - Postoperative Pain Clinical Trials

Pain Management After Cardiac Surgery - Opioids or NSAID

Start date: May 2009
Phase: Phase 4
Study type: Interventional

The aim of this randomized controlled study is to shed light on the analgesic properties and side-effect profile of an opiod-based regimen as opposed to an Ibuprofene based regimen.