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临床试验/CTRI/2025/10/096734
CTRI/2025/10/096734尚未招募不适用

Assessment of risk factors and efficacy of multifaceted intervention to prevent primary Post Partum Hemorrhage among Pregnant women.

PRINCIPAL NVESTIGATOR1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2026年1月30日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
300
试验地点
1
主要终点
The primary outcome of the study is the improvement in knowledge and preparedness regarding the prevention and early recognition of primary postpartum hemorrhage among antenatal mothers. This will be measured using a structured knowledge questionnaire administer afterthe educational intervention.

研究概览

简要总结

Post partum haemorrhage is the leading cause of  maternal death and largely preventable through  antenatal  care.This study evaluates a multifaceted intervention combining education and risk assessment to improve knowledge and preparedness thereby enhancing maternal awareness and preventing Primary Post partum Haemorrhge.

研究设计

研究类型
Observational

入排标准

年龄范围
19.00 Year(s) 至 35.00 Year(s)(—)
性别
Female

入选标准

  • Pregnant women between 16 to 28 weeks of gestation Pregnant women may be primigravida or multigravida Low to moderate PPH risk Age multiparty mild anemia Malnutrition mild Gestational Hypertension Willing to participate and available for data collection.
  • Women who provide informed consent to participate in the study or intervention.

排除标准

  • High-Risk Cases: Women identified as high-risk for PPH those with a history of PPH placenta previa or placental abruption Previous Caesarean section deliver Women who do not provide informed consent Women who are not willing to participate.

结局指标

主要结局

The primary outcome of the study is the improvement in knowledge and preparedness regarding the prevention and early recognition of primary postpartum hemorrhage among antenatal mothers. This will be measured using a structured knowledge questionnaire administer afterthe educational intervention.

时间窗: At 16-28 weeks of gestation | •One day 10 samples are selected and then to be continued for the rest days till 200 samples | •10 samples each day 20 days for 200 sample selection | •On same day educational intervention | •Then administer structured knowledge questionnaire on same day | At 32-38 weeksgroup discussion with completion of Participant | Feedback form to evaluate efficacy of intervention around 20 mothers each day so 10 days for 200 mother.

次要结局

  • reduce MMR in pph mother(prevalence after intervention)

研究者

发起方
PRINCIPAL NVESTIGATOR
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

SEEMA SARKAR

NAAC A GRADE, INDIAN NURSING COUNCIL

研究点 (1)

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