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临床试验/CTRI/2022/05/042469
CTRI/2022/05/042469进行中(未招募)未知

ED90 of Prophylactic Oxytocin Infusion During Cesarean Delivery in Non-laboring Obese vs. Non-Obese Patients: An Up-Down Sequential Allocation Dose- Response Study - None

CMS and GTBH0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
进行中(未招募)
发起方

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

  • All non-laboring parturient >18 years age will be enrolled. The two arms will include obese (body mass index >=30 kg/m2) or non-obese pregnant patients (body mass index < 30 kg/m2) posted for cesarean section under spinal anesthesia.

排除标准

  • Exclusion criteria shall be patient refusal, presence of labor (defined as cervical dilatation of 3 cm or more), use of oxytocin in the preoperative period, history of PPH or more than one previous uterine surgery as well as bleeding disorders, presence of abnormal placentation and uterine fibroid, contraindications to spinal block, such as hemodynamic instability, infection at the injection site, and coagulopathy (thrombocytopenia with platelet count <100,000/mm3 or INR >1.5).

研究者

发起方
CMS and GTBH

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