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Postoperative Pain clinical trials

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NCT ID: NCT02773602 Recruiting - Postoperative Pain Clinical Trials

Dexamethasone or Clonidine as Adjuncts to Ropivacaine for Caudal Analgesia on Analgesia Duration in Children

Start date: May 2011
Phase: Phase 4
Study type: Interventional

Comparing the duration of pain relief from caudal analgesia when adjuncts like dexamethasone, clonidine, or saline (salt water) are added to ropivacaine.

NCT ID: NCT02704715 Recruiting - Postoperative Pain Clinical Trials

Postoperative Pain in Orbital Disease and Ocular Tumor

Start date: February 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the postoperative pain after general anesthesia of orbital diseases and ocular tumor patients.

NCT ID: NCT02581293 Recruiting - Postoperative Pain Clinical Trials

Effect of Visceral and Parietal Peritoneum Suturation on Postoperative Vital Signs

Start date: March 2015
Phase: Phase 1
Study type: Interventional

In this study the investigators want to asses the effect of peritonisation at c-section on postoperative vital signs which was thought to be an indirect finding secondary to increased sympathetic activity originated from pain caused by stretched peritoneum.

NCT ID: NCT02572804 Recruiting - Postoperative Pain Clinical Trials

Comparing Rectus Sheath Catheter to Epidural Post Cystectomy

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

This is a prospective randomised controlled trial that will compare the outcomes of rectus sheath catheters to epidurals in patients who have undergone a cystectomy, via a lower midline abdominal incision for bladder cancer.

NCT ID: NCT02571153 Recruiting - Postoperative Pain Clinical Trials

Low Doses of Ketamine and Postoperative Quality of Recovery

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

There are evidences that intraoperative administration of low doses of ketamine may contribute to control the postoperative pain by acting on the NMDA channel, reducing the effects related to the tolerance and hyperalgesia induced by opioids. This study aims to evaluate the effects of administration of this agent not only as an analgesic but also its role in the quality of recovery from anesthesia, which includes observation of emotional, psychological and physical aspects. Patients who were scheduled to undergo total intravenous anesthesia (TIVA) for laparoscopic cholecystectomy will be enrolled in this clinical study. After induction of anesthesia, patients will receive one of three solutions according to the randomly selected group: ketamine 0,2 mg/kg; ketamine 0,4 mg/kg or saline. In the recovery room and on the ward, data related to the presence of pain, analgesic consumption, the incidence of nausea and vomiting, dizziness or hallucinations will be recorded. The next day, the quality of recovery will be evaluated by apllication of the questionnaire QoR40.

NCT ID: NCT02495220 Recruiting - Postoperative Pain Clinical Trials

Efficacy of Dexmedetomidine for Postoperative Analgesia in Infantile Cataract Surgery

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

The purpose of the present study was to evaluate the efficacy and safety of subtenon block (SB)anesthesia with dexmedetomidine in combination with bupivacaine versus intravenous dexmedetomidine for postoperative analgesia and emesis control in infants undergoing cataract surgery.

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: NCT02476370 Recruiting - Anxiety Clinical Trials

Effects of Preoperative Relaxation and Intensified Surgery Education in Patients Undergoing Herniotomy

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

This study aims to test the effects of a Preoperative Relaxation intervention and an Intensified Surgery Patient Education on pre- and postoperative wellbeing and health in Patients Undergoing Herniotomy.

NCT ID: NCT02424591 Recruiting - Postoperative Pain Clinical Trials

A Comparison of Intra-op Ketamine vs Placebo in Patients Having Spinal Fusion

Start date: August 2014
Phase: Phase 4
Study type: Interventional

Postoperative pain is severe after major spine surgery. Opioids such as morphine and hydromorphone are routinely used for postoperative pain control. These drugs have significant side effects, most importantly respiratory depression, nausea, constipation and tolerance. Moreover, many spine surgery patients have used opioid pain medication for back pain long term, leading to pre-surgical opioid tolerance and increased postoperative pain. This has led to a search for adjuvant medications to reduce the use of opioids and reduce opioid mediated side effects and tolerance. Ketamine is an intravenous anesthetic with analgesic properties in subanesthetic doses. Ketamine is a noncompetitive antagonist of N-methyl-D-aspartate (NMDA) receptors. NMDA receptors are involved in central pain sensitization via wind-up phenomenon and altered pain memory, a process which can be blocked by ketamine. NMDA receptor antagonists may prevent the development of tolerance to opioids and hyperalgesia. Ketamine has been safely used to decrease pain in numerous studies. Ketamine can also act as an antidepressant with hours of administration. Ketamine has rapid brain uptake and subsequent re-distribution with a distribution half-life of 10-15 minutes and an elimination half-life of 2 hours. Ketamine does not cause respiratory depression.

NCT ID: NCT02331576 Recruiting - Postoperative Pain Clinical Trials

Analgesic Effect of Perineural Fentanyl Additive to Local Anesthetics in Femoral Nerve Block

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

The purpose of this study is to evaluate the analgesic efficacy of perineural fentanyl combined with local anesthetics in the post operative pain control with continuous femoral nerve block after total knee arthroplasty.