跳至主要内容
临床试验/CTRI/2026/01/100084
CTRI/2026/01/100084尚未招募不适用

A Randomised Placebo Controlled Double Blinded Study Of Oral Zinc supplementation in Preterm Neonates with Indirect Hyperbilirubinemia

Rakshitha V1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年2月10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
60
试验地点
1

研究概览

简要总结

PRETERM NEONATS WITH INDIRECTHYPERBILIRUBINEMIA AFTER APPLYING INCLUSIO AND EXCLUSION CRITERIA ARE RANDOMLY ASSIGNED TO 2 GROUPS ONE IS INTERVENTIONAL AND OTHER IS PLACEBO GROUP AND GIVE ORAL SYRUP ZINC SULPHATE OR NORMAL SALINE 0.5ML TWICE DAILY UNTIL BILIRUBIN FALLS BELOW PHOTO THERAPY RANGE AND MEASURE TOTAL AND INDIRECT BILIRUBIN LEVELS BETWEEN TWO GROUPS AT 24 HOURS AND 48 HOURS OF INTERVENTION

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
7.00 Month(s) 至 8.00 Month(s)(—)
性别
All

入选标准

  • Preterm Neonates With Indirect Hyperbilirubinemia.

排除标准

  • RH INCOMPATIBILITY TERM NEONATES SEPSIS.

研究者

发起方
Rakshitha V
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Rakshitha V

KIMS Hospital and research Center

研究点 (1)

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