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临床试验/CTRI/2025/10/096172
CTRI/2025/10/096172尚未招募2 期

Intravenous Calcium for Facilitating Recovery in Children Hospitalized with Pneumonia and Asymptomatic Hypocalcemia: A Randomized Controlled Study

Vivek Vats1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年11月1日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
Clinical resolution of pneumonia

研究概览

简要总结

Aim of the study is to evaluate the efficacy and safety of intravenous calcium supplementation for enhancing recovery in children hospitalized with pneumonia and asymptomatic hypocalcemia where serum calcium  is less than 8.5 mg/dL. Rationale of the study is that calcium plays an essential role in the contraction of respiratory muscles, low serum calcium levels can contribute to respiratory weakness and potentially exacerbate hypoxemia and respiratory failure. Rapid correction of hypocalcemia may help improve respiratory mechanics and enhance recovery in pneumonia. It is hypothesized that giving intravenous calcium to children with pneumonia and asymptomatic hypocalcemia will show faster recovery from illness.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
2.00 Month(s) 至 5.00 Year(s)(—)
性别
All

入选标准

  • Children diagnosed with pneumonia/severe pneumonia based on WHO classification, requiring hospitalization and detected to be having asymptomatic hypocalcemia.

排除标准

  • 1.Children with known chronic comorbidities (e.g., congenital heart disease, immunodeficiency, neurological disorders).
  • 2.Severe acute malnutrition 3.Children with complicated pneumonia (Empyema, lung abscess, massive pleural effusion) 4.Children presenting with shock, convulsions, requiring resuscitation or mechanical ventilation before enrolment.
  • 5.Children who received oral/parenteral calcium within last 7 days before enrolment.

结局指标

主要结局

Clinical resolution of pneumonia

时间窗: Time for clinical resolution of pneumonia (in hours) from the time of enrolment

次要结局

  • 1.Resolution of chest retractions, or tachypnea(2.Oxygen requirement)

研究者

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

Vivek Vats

University college of medical sciences and GTB Hospital

研究点 (1)

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