A Clinical Multi-Center Study of Efficacy Analysis in Different Doses of Domperidone in Feeding Intolerance of Premature Infant (MCSDDDFI)

NCT02980250 Phase 4 COMPLETED

The purpose of this clinical multi-center study is to determine whether different doses of domperidone are effective in the treatment of feeding intolerance in premature infant

Details

Lead sponsor	Nanfang Hospital, Southern Medical University
Phase	Phase 4
Status	COMPLETED
Enrolment	118
Start date	2015-11
Completion	2017-06

Conditions

• Feeding Intolerance
• Premature Birth
• Domperidone Overdose
• Gastric Retention

Interventions

• Low dose
• normal dose
• over dose
• Glucose

Primary outcomes

• the residual glucose percentage — 7 days
  3kg/kg 5% glucose will be injected into the gastric tube .The residual glucose will be drawed out from the gastric tube after 30 min

Countries

China