CTRI/2019/11/021941招募中未知
An Open Label, Parallel Two Group Clinical Study to Evaluate the Efficacy and Safety of Stretch Mark Oil and Stretch Mark Cream in Prevention and Reduction of Stretch Marks in Pregnant Women and Post- Partum Women
试验速览
- 阶段
- 未知
- 状态
- 招募中
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
- •Aged >= 18 years at recruitment.
- •Primigravid women.
- •Singleton pregnancy.
- •Women with one of the following:
- •Pregnant women between 12â??14 weeks of gestation with absence of abdominal striae (for Group I).
- •Post-Partum women with normal and C-section delivery and visible stretch marks (will be enrolled at the time of discharge- Post-partum - Group-II)
- •Willing to participate and continue with the study follow-ups.
排除标准
- •Multigravida women (due to risk of having striae from an earlier pregnancy) or with already existing striae from earlier weight loss or any other reasons.
- •Women taking corticosteroids for any reason (due to their association with skin striae).
- •High risk pregnancy.
- •Bad obstetric history.
- •Any risk/ infection known to develop congenital anomaly in the baby (TORCH infections).
- •Multiple pregnancies (due to increased maternal weight gain and skin stretching).
- •Women with a known hypersensitivity to agents in formulation (due to risk of allergic reaction).
- •Women with known disorders or illnesses that maybe associated with striae, e.g. Marfan syndrome, Cushing syndrome.
- •Women who decline to discontinue other creams or lotions.
- •Women who are unable to give informed consent.
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