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Nausea clinical trials

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NCT ID: NCT01629992 Completed - Postoperative Pain Clinical Trials

Preoperative Counseling in Cholecystectomy

Start date: January 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The investigators examined whether a written plus verbal preoperative counseling for patients undergoing open cholecystectomy would improve perioperative symptoms such as nausea, vomiting and pain.

NCT ID: NCT01617837 Completed - Clinical trials for Postoperative Nausea and Vomiting

The Efficacy of P6 Acupressure in Reducing Postoperative Nausea and Vomiting in Patients Undergoing Craniotomy

Start date: November 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this study is to investigate if P6 acupressure may reduce postoperative nausea and vomiting in neurosurgical patients undergoing craniotomy.

NCT ID: NCT01602692 Completed - Pain, Postoperative Clinical Trials

A Comparison of Tumescence in Breast Reduction Surgery

Start date: August 2012
Phase: Phase 4
Study type: Interventional

The investigators' main hypothesis is that in breast reduction surgery, the use of tumescent solution containing both dilute lidocaine and epinephrine will lead to better control of postoperative pain, nausea, vomiting, shorter time through postoperative phases of care, quicker discharge from the hospital and lower numbers of hospital readmissions than the use of tumescent solution containing only dilute epinephrine.

NCT ID: NCT01594749 Completed - Clinical trials for Chemotherapy-Induced Nausea and Vomiting (CINV)

Efficacy and Safety of Fosaprepitant Dimeglumine in Preventing Chemotherapy-Induced Nausea and Vomiting (MK-0517-031)

Start date: September 24, 2012
Phase: Phase 3
Study type: Interventional

This study aims to demonstrate that, when given concomitantly with a 5-hydroxytryptamine 3 (5-HT3) antagonist and a corticosteroid, a single 150 mg intravenous (IV) dose of fosaprepitant given on Day 1 is superior to the control regimen of 5-HT3 antagonist and corticosteroid only, in preventing chemotherapy-induced nausea and vomiting (CINV) associated with moderately emetogenic chemotherapy (MEC).

NCT ID: NCT01592708 Completed - Clinical trials for Post-operative Nausea

Study of Anesthesia Techniques to Reduce Nausea and Vomiting After Jaw Corrective Surgery

Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether a multi-modal anesthesia and pain control protocol reduces post-operative and post-discharge nausea and vomiting (PONV and PDNV) in patients undergoing upper jaw corrective surgery.

NCT ID: NCT01556932 Completed - Nausea Clinical Trials

Randomized Trial of the Effectiveness of Topical "ABH Gel" vs. Placebo in Cancer Patients With Nausea

Start date: March 2012
Phase: N/A
Study type: Interventional

This randomized clinical trial studies ABH (lorazepam, diphenhydramine hydrochloride, and haloperidol) gel in patients with nausea. ABH gel, when absorbed into the skin, may be an effective treatment for nausea and vomiting. The general purpose of this research study is to improve the treatment of nausea and vomiting.

NCT ID: NCT01553578 Completed - Pain Clinical Trials

Healing Touch or Guided Imagery In Treating Pain, Fatigue, Nausea, and Anxiety in Patients Undergoing Chemotherapy

Start date: February 2012
Phase: N/A
Study type: Interventional

This randomized clinical trial studies healing touch or guided imagery in treating pain, fatigue, nausea, and anxiety in patients undergoing chemotherapy. Healing touch and guided imagery may help treat complications caused by chemotherapy. It is not yet known whether healing touch or guided imagery is more effective in treating pain, fatigue, nausea, and anxiety in patients undergoing chemotherapy

NCT ID: NCT01544959 Completed - Breast Cancer Clinical Trials

Postoperative Analgesia Impact of Narcotic Free Anesthesia

PAINFree
Start date: January 2010
Phase: N/A
Study type: Interventional

The first hypothesis of the study is that substituting fentanyl by esmolol and metoprolol during general anesthesia for patients undergoing mastectomy will result in less pain and less narcotic consumption in the recovery room. The investigators will also verify the impact of that substitution on nausea and vomiting, on the time spent in the recovery room and on chronic postsurgical pain (3 and 6 months). Finally, the investigators will see the impact on breast cancer recurrence 5 years after the surgery.

NCT ID: NCT01543945 Completed - Clinical trials for Postoperative Nausea and Vomiting

Prevention Post Operative Nausea Vomiting in Ambulatory Gynecologic Laparoscopy

Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the incidence of Postoperative nausea and vomiting between the intervention group who received multimodal antiemetic management and the control group who did not get this protocol.

NCT ID: NCT01534637 Completed - Nausea Clinical Trials

Aprepitant in Preventing Nausea and Vomiting in Patients Undergoing Chemotherapy and Radiation Therapy for Pancreatic Cancer

Start date: August 2006
Phase: Phase 2
Study type: Interventional

This pilot clinical trial is studying how well aprepitant works in preventing nausea and vomiting in patients undergoing chemotherapy and radiation therapy for pancreatic cancer. Antiemetic drugs, such as aprepitant may help lessen or prevent nausea and vomiting in patients receiving chemotherapy and radiation therapy