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Vomiting clinical trials

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NCT ID: NCT01055236 Completed - Nausea Clinical Trials

Hydroxyzine for the Prevention of Pruritus From Spinal Morphine in Transabdominal Hysterectomy Patients

TAH
Start date: August 2007
Phase: Phase 4
Study type: Interventional

Hydroxyzine is one of antihistamines that antagonizes H1 receptor, and it's effects are reducing pruritus, nausea/vomiting, and the mild effect of sedation.With these effects Hydroxyzine should be used in the prevention of these symptoms.

NCT ID: NCT01054495 Not yet recruiting - Nausea Clinical Trials

Placebo in Acupuncture

Start date: February 2010
Phase: Phase 2
Study type: Interventional

Placebo control in acupuncture research is challenging and difficult. The primary objective of the study is to explore a study design comparing stimulation by real acupuncture needle, sham acupuncture needle and laser. The research question is whether a patient is capable of discriminate different stimulation modality when studying acupuncture stimulation for nausea in early pregnancy. The study is planned as a pilot study including 20 women in each of the three study groups, all-together 60 pregnant women. Intervention will consist of standardised 15 minutes stimulation of acupuncture point pericardium 6 by, either two acupuncture needles, two sham acupuncture needle or two laser devices. All participating women are told that they will get different stimulation at an acupuncture point with potential effect on nausea. The women will record their daily symptoms during a 4 day run-in period, a 3 day intervention period, and thereafter a 4 day follow-up period after treatment in accordance with previous research methodology. In addition, the women will record how they experience the three different stimulations of acupuncture points. The results from the study could be important for planning of future studies where the blinding issue with regard to acupuncture is challenged.

NCT ID: NCT01054456 Completed - Clinical trials for Patients With Confirmed Malignant Disease to Receive Low Emetogenic Chemotherapy (LEC) or Who Experienced at Least Nausea and Vomiting During Last Cycle of LEC

A Study of Palonosetron for the Prevention of Chemotherapy-Induced Nausea and Vomiting (CINV) in Participants Who Have Experienced CINV(Chemotherapy-Induced Nausea and Vomiting) During the Previous Cycle of Low Emetogenic Chemotherapy (LEC)

Start date: October 27, 2009
Phase: Phase 2
Study type: Interventional

This study is designed to assess the safety and efficacy of palonesetron in preventing chemotherapy-induced nausea and vomiting (CINV) when administered to participants who have experienced either vomiting and or at least moderate nausea during their last cycle of low emetogenic chemotherapy.

NCT ID: NCT01052844 Completed - Vomiting Clinical Trials

Gabapentin in the Prevention of Nausea and Vomiting Induced by Chemotherapy

Start date: January 2009
Phase: Phase 3
Study type: Interventional

Gabapentin is an antiepileptic drug. Its antiemetic effect is demonstrated after laparoscopic surgery, but it is not yet known whether gabapentin is effective in preventing chemotherapy induced emesis. The purpose of this study is to determine whether the addition of gabapentin to dexamethasone plus ondansetron increase the control of chemotherapy-induced nausea and vomiting.

NCT ID: NCT01047371 Completed - Pain Clinical Trials

Why in Hospital - Factors Determining Time to Discharge Readiness After Arthroplasty Surgery

Start date: January 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate patient related factors determining length of stay in hospital after arthroplasty surgery.

NCT ID: NCT01046461 Unknown status - Clinical trials for Postoperative Nausea and Vomiting

Ramosetron, Aprepitant and Dexamethasone (RAD) in Solid Cancer

RAD
Start date: January 2010
Phase: Phase 2
Study type: Interventional

Cisplatin is one of the most emetogenic drugs used in clinical practice and it could result in poor compliance with chemotherapy. The 5-HT3 receptor antagonists prevent vomiting in acute phase emesis after chemotherapy in 73 - 92% of cisplatin-treated patients when coadministered with steroids, but they appear to lack efficacy in the delayed phase emesis. Ramosetron, a new 5-HT3 receptor antagonists, has been shown to have equivalent efficacy and tolerability and a longer duration of effect than granisetron in preventing acute vomiting in patients undergoing cisplatin-containing chemotherapy. Acute phase emesis was prevented in 84.8% of patients receiving ramosetron plus dexamethasone, but the CR rate of total phase emesis was less than 60%. Aprepitant is a selective, high-affinity NK1 receptor antagonist. Adding aprepitant to 5-HT3 receptor antagonists and steroid improve CR rate of not only chemotherapy induced acute emesis and but also delayed emesis by 11-14 and 20 percentage points, respectively. But until now, there was no information that which 5-HT3 receptor antagonists is the best partner for aprepitant. Therefore, we initiated a prospective, open-label, phase II study to assess the efficacy and tolerability of a combination of ramosetron, aprepitant and dexamethasone (RAD) in the prevention of cisplatin based CINV in chemotherapy-naïve patients with solid cancer

NCT ID: NCT01041183 Unknown status - Nausea Clinical Trials

The Effect of Oral and Intravenous Ramosetron During Laparoscopic Cholecystectomy

Start date: November 2009
Phase: N/A
Study type: Interventional

Patients undergoing general anesthesia for laparoscopic cholecystectomy have a high risk of postoperative nausea and vomiting (PONV). The investigators investigated the effect of oral and IV ramosetron on PONV prophylaxis after laparoscopic cholecystectomy.

NCT ID: NCT01031953 Terminated - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

Fosaprepitant Dimeglumine in Treating Patients With Nausea and Vomiting Caused By Chemotherapy

Start date: August 2008
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Antiemetic drugs, such as fosaprepitant dimeglumine, may help lessen or prevent nausea and vomiting in patients treated with chemotherapy. PURPOSE: This clinical trial is studying the side effects of fosaprepitant dimeglumine and to see how well it works in treating patients with nausea and vomiting caused by chemotherapy.

NCT ID: NCT01031498 Completed - Clinical trials for Acute Myelogenous Leukemia

Palonosetron Versus Ondansetron for the Prevention of Nausea and Vomiting

Start date: September 2005
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to compare the effectiveness of 3 drug schedules in preventing chemotherapy-related nausea and/or vomiting in patients with acute myelogenous leukemia (AML) or high-risk myelodysplastic syndrome (MDS).

NCT ID: NCT01030614 Completed - Postoperative Pain Clinical Trials

Dexamethasone Improves Postoperative Symptoms After Laparoscopic Cholecystectomy

dxt
Start date: January 2007
Phase: Phase 3
Study type: Interventional

Dexamethasone has been reported to reduce postoperative nausea and vomiting (PONV) after laparoscopic cholecystectomy (LC). However, its effects on other surgical outcomes such as pain and fatigue have been unclear. We evaluated the efficacy of preoperative dexamethasone in ameliorating postoperative symptoms after LC. Methods: Prospective, double-blind, placebo-controlled study, 210 patients scheduled for elective LC were analyzed after randomization to intravenous dexamethasone (8 mg) or to a placebo. All patients underwent standardized procedures for general anesthesia and surgery. Episodes of PONV and pain and fatigue scores were recorded on a visual analogue scale. Analgesic and antiemetic requirements were also recorded.