Randomised controlled trial of acetate in preterm neonates receiving parenteral nutrition

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

ISRCTN

Registry ID

ISRCTN58031154

Enrollment

Registered

2004-01-23

Start date

1995-07-01

Completion date

Unknown

Last updated

2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neonatal diseases Neonatal Diseases

Interventions

Standard parenteral nutrition vs novel formulation with replacement of any chloride dose >3 mmol/kg/day as acetate

Eligibility

Inclusion criteria

Inclusion criteria: Preterm neonates under 32 weeks gestation were entered into the study if they were still receiving intravenous glucose/electrolyte solution on day 3, but not receiving enteral nutrition.

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

Measure	Time frame
Not provided at time of registration	—

Secondary

Measure	Time frame
Not provided at time of registration	—

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026