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临床试验/NCT04926727
NCT04926727Unknown不适用

Prevalence And Burden Of Nausea And Vomiting In Pregnant Women. An Italian Survey (PURITY)

Italfarmaco3 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2021年10月4日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
600
试验地点
3
主要终点
Percentage of cases based on PUQE

研究概览

简要总结

On February 25th, 2019, ITALFARMACO launched Nuperal® in Italy, an association of doxylamine succinate and pyridoxine hydrochloride authorized by AIFA for the symptomatic treatment of nausea and vomiting in pregnancy (NVP). This drug is also recommended as first choice drug therapy by the American College of Obstetricians and Gynecologists (ACOG) Guidelines and is supported by extensive international literature.

Numerous epidemiological researches conducted in the US and Norway have highlighted the extent of vomiting and pregnant nausea. Unfortunately to date, there are no information on the prevalence of this phenomenon in Italy, on its impact on women's lives and on the interaction between woman and gynecologists.

The research hypothesis of the present survey is that, using a representative sample of pregnant women in Italy, it will be possible to identify the prevalence and weight of nausea and vomiting symptoms during pregnancy in this country. The study is an open, non-comparative, multicenter survey and the aim is to evaluate the prevalence and weight that the symptoms of nausea and vomiting have in pregnant women in Italy.

The study population will include 600 women found during weeks 18-22 of pregnancy who will arrive at the three sites or will contact the Investigators after the Ethics Committee (EC) approval.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Caucasian women in physiological pregnancy and between the 18th and 22nd week (time of morphological ultrasound).
  • Women able to communicate adequately with the interviewer and understand the questionnaires.
  • Women able to understand and who can provide valid informed consent to the Survey.

排除标准

  • Twin pregnancy.
  • Medically assisted procreation (MAP)

结局指标

主要结局

Percentage of cases based on PUQE

时间窗: 18 to 22 weeks

Percentage of mild, medium and severe cases based on PUQE.

NVP related questions

时间窗: 18 to 22 weeks

Percentage of answer allocation to Nausea Vomiting Pregnancy related questions

Mean and SD of onset for each symptom and its duration

时间窗: 18 to 22 weeks

Mean and Standard Deviation of onset for each symptom and its duration

Correlation with the use of both therapies

时间窗: 18 to 22 weeks

Correlation of the use of non-pharmacological, pharmacological or both therapies with the severity of the symptoms during pregnancy and with the possible outcomes.

Correlation between severity of symptoms and consequences on women's personal life.

时间窗: 18 to 22 weeks

Correlation between severity of symptoms and consequences on women's personal life (family, work, etc.).

Correlation between symptoms in pregnancy and outcomes based on data from the post pregnancy questionnaire

时间窗: 18 to 22 weeks

Correlation between symptoms in pregnancy (and relative severity) and outcomes based on data from the post pregnancy questionnaire (weight of new-born, gestational age at birth and any complications).

NVP prevalence.

时间窗: 18 to 22 weeks

Nausea, vomiting pregnancy prevalence

Number of cases with hospitalization

时间窗: 18 to 22 weeks

Number of cases with hospitalization in relation to total and severity of symptoms (PUQE).

Correlations between demographic data and the presence of symptoms

时间窗: 18 to 22 weeks

Correlations between demographic data (age, first pregnancy status, multiparity, geographical origin, type of work and educational qualification) and the presence of symptoms and their severity.

次要结局

未报告次要终点

研究者

发起方
Italfarmaco
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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