CTRI/2010/091/002807已完成2 期
A RANDOMIZED CONTROLLED TRIAL TO EVALUATE THE IMMUNOGENICITY OF TWO DOSES OF THE MODIFIED KILLED WHOLE CELL ORAL CHOLERA VACCINE (WC-OCV) UNDER TWO ALTERNATIVE VACCINATION SCHEDULES
International Vaccine InstituteSeoul Korea0 个研究点目标入组 386 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 386
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Healthy, non-pregnant adults aged 18 years and above and healthy children aged 1 - 17 will be recruited in Kolkata.
- •All subjects must satisfy the following criteria at study entry:
- •1.Males or non-pregnant females aged 18 years and above and children aged 1 -17 years who the investigator believes will comply with the requirements of the protocol (i.e. available for follow-up visits and specimen collection).
- •2.Written informed consent obtained from the subjects or their parents/guardians, and written assent for children aged 12 ? 17 years.
- •3.Healthy subjects as determined by:
- •Medical history
- •Physical examination
- •Clinical judgment of the investigator
排除标准
- •The following criteria should be checked at the time of study entry, if any of the following is present then the subject will be excluded from the study:
- •1.Ongoing serious chronic disease
- •2.For females of reproductive age: Pregnancy (or females planning to become pregnant during the study period; as determined by verbal screening)
- •3.Immunocompromising condition or therapy (for corticosteroids this would mean ≥0.5 mg/kg/day)
- •4.Diarrhea (3 or more loose/watery stools within a 24-hour period) 6 weeks prior to enrollment
- •5.One or two episodes of diarrhea lasting for more than 2 weeks in the past 6 months
- •6.One or two episodes of abdominal pain lasting for more than 2 weeks in the past 6 months
- •7.Intake of any anti-diarrhea medicine in the past week
- •8.Abdominal pain or cramps, loss of appetite, nausea, general ill-feeling or vomiting in the past 24 hours
- •9.Acute disease one week prior to enrollment, with or without fever. Temperature ≥38ºC warrants deferral of the vaccination pending recovery of the subject
- •10.Receipt of immunoglobulin or any blood product during the past 3 months
- •11.Receipt of antibiotics in past 14 days
- •12.Receipt of live or killed enteric vaccine in past 4 weeks
- •13.Receipt of killed oral cholera vaccine
研究者
相似试验
已完成
2 期
EFFECTIVENESS OF A NURSING INTERVENTION PROGRAMME(NURSE NAVIGATOR PROGRAMME) IN BREAST CANCER PATIENTSCTRI/2015/09/006192MANIPAL COLLEGE OF NURSING MANIPALMANIPAL UNIVERSITY120
已完成
2 期
Testing of boosting capacity of Shancol, a killed whole cell oral cholera vaccine,in previously vaccinated children and adults .CTRI/2012/04/002574International Vaccine Institute426
招募中
Unknown
Evaluating an In-Person, Clinician-Facilitated and an Online, Guided Self-Help Program for University Students with Social AnxietyMental Health - AnxietySocial Anxiety DisorderACTRN12624000720516Professor Elizabeth Rieger90
已完成
不适用
A Randomized Controlled Trial of a Functioning Improved Tool home visit program for Japanese frail older peopleJPRN-UMIN000010325Hokkaido University Graduate School of Medicine90
已完成
不适用
The Randomized Controlled Trial for Evaluating the Efficacies of Tolvaptan in Patients with Chronic Kidney Diseasechronic kidney diseaseJPRN-UMIN000014763Yokohama City University Medical Center Yokohama City University Hospital50
