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Nausea clinical trials

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NCT ID: NCT03185156 Completed - Nausea and Vomiting Clinical Trials

The Preventive Effects of Sub Hypnotic Dose of Propofol for Nausea and Vomiting Induced by Hemabate

Start date: June 28, 2017
Phase: Phase 4
Study type: Interventional

This is a randomized, placebo-controlled trail, the objective of this study is observation the effect of sub hypnotic dose of propofol for prevention of nausea and vomiting induced by hemabate during spinal anesthesia for elective cesarean section. The primary outcome is the presence of post-delivery intra-operative nausea and vomiting in parturients. The patients demographic characteristics, blood pressure, sensory block level, and the medications will be collected.

NCT ID: NCT03178058 Recruiting - Clinical trials for Postoperative Nausea and Vomiting

Risk Factors for Postoperative Nausea, Vomiting and Pruritus

Start date: October 2016
Phase: N/A
Study type: Observational

In this study we would like to identify demographic and individual risk factors that place parturients at a higher risk for postoperative nausea and vomiting (PONV) and itching following administered neuraxial morphine for cesarean section. Our primary objective is to develop a reliable predictive neuraxial morphine induced nausea and vomiting (NMINV) and itching model.

NCT ID: NCT03171688 Completed - Clinical trials for Postoperative Nausea and Vomiting

Risk Factors for Nausea and Vomiting After Cesarean

Start date: May 1, 2016
Phase:
Study type: Observational

Investigators will observe the incidence of post-cesarean nausea or vomiting and try to associate it with some risk factors.

NCT ID: NCT03165123 Not yet recruiting - Clinical trials for Post-operative Nausea and Vomiting

Effect of Using Azithromycin Versus Placebo With Dexamethasone in Prevention of Post-spinal Nausea and Vomiting.

Start date: June 1, 2019
Phase: Phase 4
Study type: Interventional

Postoperative nausea and vomiting is defined as any nausea, retching, or vomiting occurring during the first 24-48 h after surgery in inpatients. Postoperative nausea and vomiting is one of the most common causes of patient dissatisfaction after anesthesia, with reported incidences of 30% in all post-surgical patients and up to 80% in high-risk patients. In addition, postoperative nausea and vomiting is regularly rated in preoperative surveys, as the anesthesia outcome the patient would most like to avoid. While suture dehiscence, aspiration of gastric contents, esophageal rupture, and other serious complications associated with postoperative nausea and vomiting are rare, nausea and vomiting is still an unpleasant and all-too-common postoperative morbidity that can delay patient discharge from the post-anesthesia care unit and increase unanticipated hospital admissions in outpatients.

NCT ID: NCT03145727 Recruiting - Clinical trials for Breast Cancer Female

Electric Stimulation on Nausea and Vomit Chemotherapy Induced

TENS-NV
Start date: August 1, 2017
Phase: N/A
Study type: Interventional

Chemotherapy induces nausea and vomit for some large patients. But, some chemotherapy protocol has a high indices of the incidence as observed in a combination of Anthracycline and Cyclophosphamide (AC). To prevent this symptoms, some medication can be used as Ondansetron. By other hands, the traditional acupuncture on Chinese Medicine have been used a PC6 point to avoid nausea and vomit. More recently, a transcutaneous electric nerve stimulation (TENS) also has been used for this application. Our study will test the TENS applied on PC6 point with two different frequencies (high and low) to evaluated the nausea and vomit inhibition effects.

NCT ID: NCT03143829 Completed - Neoplasms Clinical Trials

Promoting Cancer Symptom Management in Older Adults

Start date: August 11, 2016
Phase: N/A
Study type: Interventional

The purpose of the project is to estimate the effect size of a technology based intervention for older adults with cancer for nausea and vomiting. Participants will be randomized to either an intervention or a wait control group. Outcomes such as symptom severity, quality of life and resource use will be examined.

NCT ID: NCT03141645 Completed - Clinical trials for Postoperative Nausea and Vomiting

Comparison of IV Fluid Loading and Ondansetron in Reduction of PONV After LC

Start date: June 20, 2017
Phase: N/A
Study type: Interventional

This study is designed to examine the incidence of postoperative nausea and vomiting during 24 hours after elective laparoscopic cholecystectomy in patients receiving preoperative intravenous fluid loading (group F), ondansetron (group O) and receiving neither fluid nor ondansetron or control group (group C).

NCT ID: NCT03139383 Completed - Clinical trials for Postoperative Nausea and Vomiting

Dextrose Containing Fluid and the Postoperative Nausea and Vomiting in the Gynecologic Laparoscopic Surgery

Start date: September 30, 2014
Phase: N/A
Study type: Interventional

The investigators tested the hypothesis that administration of intravenous dextrose as a maintenance fluid in gynecologic laparoscopic surgery would reduce the incidence and severity of postoperative nausea and vomiting (PONV) compared with normal saline solution in the same dose. A prospective randomized double blinded controlled study was conducted. Eighty six participants were randomized to dextrose solution (n= 42) or normal saline solution (n= 44). The Bellville postoperative nausea and vomiting scores were recorded until 24 hours after surgery.

NCT ID: NCT03137121 Completed - Advanced Cancer Clinical Trials

Olanzapine for the Treatment of Chronic Nausea and/or Vomiting in Advanced Cancer Patients

Start date: July 12, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the use of olanzapine for the treatment of cancer patients with chronic nausea and/or vomiting unrelated to chemotherapy or radiation in a randomized placebo-controlled pilot trial.

NCT ID: NCT03130218 Completed - Clinical trials for Bariatric Surgery Candidate

Aromatherapy in Management of Postoperative Nausea in Post-Bariatric Surgery Patients

Start date: June 8, 2017
Phase: N/A
Study type: Interventional

Determine the effectiveness of peppermint oil aromatherapy in relieving post-operative nausea in the bariatric surgery patient population.