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Effect of cisapride on gastric emptying in premature infants with feed intolerance
C P Barnett1, T Omari, G P Davidson
1Neonatal Medicine Unit, Women's and Children's Hospital, North Adelaide, Australia. barnettc@wch.sa.gov.au
Insights
Cisapride did not improve gastric emptying or reflux symptoms in preterm infants with feeding intolerance. The drug was associated with slower infant growth, and its use is not recommended.
Area of Science:
- Neonatalogy
- Pediatric Gastroenterology
- Pharmacology
Background:
- Feed intolerance is a common issue in preterm infants.
- Gastro-oesophageal reflux (GOR) and delayed gastric emptying contribute to feeding intolerance.
- Cisapride is a prokinetic agent that may improve gastrointestinal motility.
Purpose of the Study:
- To evaluate the efficacy of cisapride in preterm infants with feed intolerance.
- To assess the impact of cisapride on gastric emptying and GOR symptoms.
Main Methods:
- A randomized, placebo-controlled crossover study involving 16 preterm infants (24-35 weeks gestational age).
- Infants received cisapride (0.2 mg/kg four times daily) or placebo for 7 days, followed by a crossover period.
- Gastric emptying was measured using the [13C]-octanoic acid breath test; GOR symptoms were monitored via a standardized chart.
Main Results:
- No significant difference in gastric emptying (t1/2: 31.9 ± 4.7 min vs. 34.2 ± 3.9 min, P = 0.65) between cisapride and placebo.
- Infants receiving cisapride exhibited slower growth rates.
- No improvement in gastro-oesophageal reflux symptoms was observed with cisapride treatment.
Conclusions:
- Cisapride does not improve gastric emptying or reduce GOR symptoms in preterm infants with feed intolerance.
- The potential for adverse effects on growth suggests cisapride should not be recommended for this patient population.
- Further research may be needed to explore alternative treatments for feed intolerance in preterm neonates.
Objective:
To assess the effect of cisapride on gastric emptying and gastro-oesophageal reflux (GOR) symptoms in preterm infants with feed intolerance.
Methods:
Sixteen preterm infants (gestational age 24-35 weeks) with feed intolerance were enrolled in the study. Infants were randomized to receive 7 days of cisapride 0.2 mg/kg four times a day, immediately followed by 7 days of placebo or vice versa. Gastric emptying was measured using the [13C]-octanoic acid breath test prior to study entry and repeated on day 5, 6 or 7 after randomization and 5, 6 or 7 days after crossover. The symptoms of GOR were monitored during the study period using a standardized reflux chart. Weight was recorded daily.
Results:
There was no change in gastric emptying in infants prescribed cisapride (gastric half-emptying time (t1/2) 31.9 +/- 4.7 vs 34.2 +/- 3.9 min for placebo vs cisapride, respectively; P = 0.65). Infants on cisapride had slower growth and there was no change in reflux symptoms.
Conclusions:
The use of cisapride in preterm infants with feed intolerance cannot be recommended.
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