Efficacy of Ginger on Intraoperative and Postoperative Nausea and Vomiting in Elective Cesarean Section Patients.
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 239
- 试验地点
- 1
- 主要终点
- Occurrence of Intra-operative and Post-operative Vomiting
研究概览
简要总结
SPECIFIC AIMS
- Assess risk factors for nausea and vomiting in c-section patients undergoing regional anesthesia
- Quantify the incidence of nausea and vomiting intraoperatively and postoperatively in the ginger and placebo groups.
- Quantify post-operative analgesia and pruritus in the ginger and placebo groups
- Quantify patient satisfaction of the ginger and placebo groups
- Assess patient expectation of ginger on post-op day three
详细描述
Two hundred and thirty nine ASA class I and II patients, scheduled for elective c-section will be assigned randomly to receive either 1g ginger tablet PO (Group 1) or 1 g placebo PO (Group 2) preoperatively, immediately before surgery. The usual preoperative anti-emetic and antacid regimen will be continued for both groups. Initial blood pressure, pulse and hemoglobin and hematocrit will be documented by the researcher prior to the arrival of the patient into the operating room. A baseline questionnaire will be given to the patients to assess risk factors for nausea and vomiting. Questions will include: age, BMI, parity, weeks gestation, h/o seasickness, h/o of hyperemesis gravidrum in this or prior pregnancies, h/o PONV, medical problems, any medication used within past 24 hrs, education and occupation.
Intraoperatively, both groups will receive combined spinal-epidural anesthesia in the usual manner. All standard monitoring will be applied and vital signs recorded for the entirety of the procedure. The number and dose of ephedrine or phenylephrine boluses and the number and severity of nausea episodes (using a Visual Analog Scale (VANS)) and number of vomiting episodes will be noted. In addition the following will be recorded: if uterus was exteriorized, any medications used by the anesthesiologist (other than ephedrine and phenylephrine), and estimated blood loss.
Postoperatively, patients will receive either a one time dose of the 1g ginger PO (Group 1) or 1 g placebo PO (Group 2) 2 hours after entering the postanesthesia care unit (PACU). Thirty minutes after the medication is given, patients will be asked to rate their nausea, level of analgesia, and level of pruritus on a VANS, and vomiting episodes will be recorded. Medications given for nausea will be continued in the post-operative period for both groups. The doses of Zofran will be counted in the 24 hr postoperative period. Twenty-four hours after surgery, blood will be drawn to assess hemoglobin and hematocrit as well as to assess platelet function.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 49 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Healthy (i.e., ASA I, or II) patients presenting for planned c-section at New York Methodist Hospital
- •Signed informed consent
排除标准
- •They are unable or unwilling to take part in the study
- •They have a history of an allergy to any medications used including ginger
- •They have had any gastrointestinal surgery on the stomach, small intestine, or gall bladder.
- •They have any history of bleeding disorder, (i.e., Hemophilia A/B, ITP, etc.)
- •They have a contraindication to intrathecal or epidural anesthesia. ( i.e., Arnold- Chiari malformation, etc.)
- •They are unable to understand instructions or questions related to study
- •ASA III or IV patients
研究组 & 干预措施
Placebo
2 gm of placebo pill (A capsule)
干预措施: Placebo Oral Tablet (Drug)
Ginger
2 gm powder of ginger filled in a capsule
干预措施: Ginger (Drug)
结局指标
主要结局
Occurrence of Intra-operative and Post-operative Vomiting
时间窗: During surgery (1 hour) and thru 72 hours after surgery
Participants who had intra-operative and post-operative vomiting were identified and compared between the two groups.
次要结局
未报告次要终点
研究者
Joel Yarmush
Attending Physician, Program Director (Anesthesiology)
New York Presbyterian Brooklyn Methodist Hospital