Seok 1998.
| Methods | Single‐centre randomized controlled trial |
| Participants |
Inclusion criteria
|
| Interventions |
Active intervention (n = 23) Indomethacin 0.2 mg/kg initial dose followed by 2 doses of 0.1 mg/kg at 24‐hour intervals. 15 participants received IV formulation and 8 received oral formulation Control (n = 23) No placebo |
| Outcomes | Primary outcome: germinal matrix or intraventricular haemorrhage |
| Notes |
Primary study location: Il Sin Christian Hospital, Pusan, Korea Study Period: August 1995 to June 1997 The article is in Korean. We are awaiting translation of the article from Korean to English |
GA: gestational age;GI: gastrointestinal; IVH: intraventricular haemorrhage; NEC: necrotizing enterocolitis; PDA: patent ductus arteriosus.