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Nausea clinical trials

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NCT ID: NCT02007109 Completed - Clinical trials for Postoperative Nausea and Vomiting

Use of Baxter Animated Retching Faces (BARF) Scale to Measure Nausea in Children Who Speak Spanish

Start date: January 2014
Phase:
Study type: Observational

Pediatric research in the management of nausea has been limited by the absence of a reliable method to quantify the intensity of this subjective symptom. In adults, the visual analog scale (VAS) is an accurate tool, but this has not been shown to be reliable in young children. A scale is a series of points made on a line that will be used for measurement; a mark on the far left of the line shows little pain and the mark on the far right means alot of pain.

NCT ID: NCT02006056 Completed - Nausea Clinical Trials

Ondissolve in the Prophylaxis/Rescue of Radiation Induced Nausea and Vomiting

Start date: November 2013
Phase: Phase 2
Study type: Interventional

The primary objective of the study is to examine the efficacy of Ondissolve for the prevention/rescue of Acute and Delayed Phase radiation induced nausea and vomiting (RINV) in patients undergoing single or multiple fraction, emetogenic palliative radiation therapy for painful bone metastases. The study population will be 30 patients seen in the RRRP at the Sunnybrook Odette Cancer Centre receiving palliative radiation therapy considered emetogenic for bone metastases. Patients will take the study medication (Ondissolve 8 mg) twice on each day of radiation therapy, at least one hour prior to treatment and repeat approximately 6-8 hours later the same day. Patients undergoing multiple fraction radiation therapy will take Ondissolve on weekends or holidays in between treatment. Secondary objectives include to evaluate key secondary endpoints related to RINV, and to investigate the ease and length of administration of protocol medicine. We hypothesize that Ondissolve will be effective in the prophylaxis of RINV, and the ease of use and administration will provide an appropriate delivery method for those unable to tolerate the oral form of ondansetron.

NCT ID: NCT02001948 Completed - Postoperative Pain Clinical Trials

Intrathecal Morphine for Inguinal Hernia Repair.

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

The aim of this study was to compare the effects of two different doses of intrathecal morphine (0.1 mg and 0.4 mg) combined with 7.5 mg of heavy bupivacaine on postoperative block regression times, postoperative analgesia and the severity of side effects, for inguinal hernia repairs.

NCT ID: NCT01993381 Recruiting - Clinical trials for Chemotherapy-induced Nausea and Vomiting

Evaluation of Predictive Risk Factors of Chemotherapy-induced Nausea and Vomiting

Start date: November 2013
Phase: N/A
Study type: Observational

The most common toxicity of chemotherapy is nausea and vomiting, and appropriate management of these toxicities can help patients improve tolerance for chemotherapy. Anti-emetics including dopamine antagonist, serotonin antagonist, and substance P antagonist administered to patients according to emetogenic risk of chemotherapeutic drugs. However, patients don't always experience same nausea and vomiting for the same drugs. Therefore, it is important to determine the biomarker to predict chemotherapy-induced nausea and vomiting. Some biomarkers studies were done during the chemotherapy. However it is not definite evidence of relations between biomarkers and chemotherapy. We will hope to find any predictive biomarker of CINV.

NCT ID: NCT01991223 Recruiting - Pain Clinical Trials

Dexmedetomidine for Catheter-related Bladder Discomfort

CRBDEX
Start date: November 2013
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy of dexmedetomidine for the prevention of catheter-related bladder discomfort

NCT ID: NCT01988194 Completed - Depression Clinical Trials

Pragmatic Research eXamining Inpatient Symptoms

PRAXIS
Start date: November 2013
Phase: N/A
Study type: Interventional

Many hospitalized patients experience pain during their hospital stay, and less than half report adequate pain relief. Common treatments for pain include opioid medications, which have associated side effects and complications. Research has shown that acupuncture is effective for surgical, postoperative and cancer-related pain, nausea, and vomiting. More research is needed on the effectiveness of adding acupuncture to routine care for hospitalized patients. The objective of this study is to examine the effectiveness of acupuncture delivered in a "real-world" setting according to the principles of traditional Chinese medicine among hospitalized patients to manage pain and other symptoms. 250 hospitalized participants will be randomized in a 1 to 1 ratio to receive either 1) usual care or 2) usual care with acupuncture offered (125 in each group). The primary outcome measure will be change in daily pain intensity. Data on other symptoms, such as nausea, vomiting, anxiety, and depression, as well as functionality and quality of life will be collected in person, on a web-based survey, or via telephone follow-up. The aims of the study are to examine the effectiveness of acupuncture to manage pain and other symptoms among hospitalized patients; to evaluate the impact of acupuncture on patient satisfaction among hospitalized patients; and to estimate costs and cost-effectiveness of acupuncture among a subset of hospitalized patients. The investigators hypothesize that compared to hospitalized patients receiving usual care alone, hospitalized patients receiving acupuncture will have: 1. decreased pain severity 2. higher patient satisfaction

NCT ID: NCT01987869 Recruiting - Nausea Clinical Trials

Hiperemezis and Serotonin Elevated Serum Serotonin Levels in Hyperemesis

Start date: October 2013
Phase: N/A
Study type: Observational

Serotonin excretion was investigated in the nausea and vomiting associated with hiperemezis gravid arum.

NCT ID: NCT01984931 Recruiting - Nausea Clinical Trials

Study of Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)for Treatment of Post Operative Nausea and Vomiting

Start date: October 2013
Phase: Phase 3
Study type: Interventional

This study will determine if giving Trimebutine Maleate (NEWBUTIN SR 300 mg Tab)orally will be effective as a prophylactic anti-emetic drug for patients who underwent arthroscopic rotator cuff repair under general anesthesia.

NCT ID: NCT01980160 Withdrawn - Nausea Clinical Trials

Relief Band as an Adjunct to Antiemetic Therapy in Patients Who Receive Mod to Highly Emetogenic Chemotherapy

Start date: November 2013
Phase: N/A
Study type: Interventional

The primary study hypotheses are that, without increasing doses of breakthrough medications or device intolerance, the Nometex™ device worn for 5-days beginning with the day of chemotherapy administration in women with ovarian or advanced endometrial or cervical cancer will, as an adjunct to standard-of-care anti-emetics, reduce vomiting episodes, and reduce the severity of nausea. The secondary hypotheses are that the Nometex™ device reduces acute (Day 1) emetic episodes, day 1 and days 2-5 severity of nausea, and delayed (days 2-5) emetic episodes without increasing doses of breakthrough medications or device intolerance.

NCT ID: NCT01975727 Terminated - Clinical trials for Postoperative Nausea and Vomiting

Dexamethasone for the Treatment of Established Postoperative Nausea and Vomiting

DexPonv
Start date: September 3, 2012
Phase: Phase 2
Study type: Interventional

Postoperative nausea and vomiting (PONV) are frequent after surgery and anaesthesia. Dexamethasone is widely used as antiemetic for the prevention of PONV. Little is known about the efficacy of antiemetic drugs for the treatment of established PONV symptoms. No single randomised trial has been published so far that tests the efficacy of dexamethasone for the treatment of established PONV symptoms. In this trial the investigators want to test the antiemetic efficacy of three different doses of intravenous dexamethasone for the treatment of established PONV symptoms. In adjunct protocols of this study the investigators aim to establish a novel method to quantify the anti-nausea efficacy of an antiemetic drug, to study pharmacogenetics of PONV, and to further our understanding on the smoking status as a predictive factor of PONV.