Placental Growth Factor Led Management of the Small for Gestational Age Fetus: Randomised Controlled Feasibility Study

Bullough, S orcid iconORCID: 0000-0002-1660-5245, Dower, M, Jackson, R, Heazell, AEP orcid iconORCID: 0000-0002-4303-7845, Woolfall, K, Andronis, L orcid iconORCID: 0000-0001-7998-7431, Kenny, L, Alfirevic, Z, Sharp, A orcid iconORCID: 0000-0003-3396-7464, PLANES study group and Doughty, H (2025) Placental Growth Factor Led Management of the Small for Gestational Age Fetus: Randomised Controlled Feasibility Study. BJOG : An International journal of obstetrics and gynaecology. ISSN 1470-0328

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Open Access URL: https://doi.org/10.1111/1471-0528.70106 (Published version)

Abstract

Objective
To determine the feasibility of a trial investigating the optimal timing for the birth of women with a suspected late preterm and term SGA baby using either angiogenic biomarker-led care or standard care.

Design
A mixed methods study including a randomised feasibility trial, interviews, questionnaires and economic analysis.

Setting
Two tertiary maternity hospitals in the UK.

Population
Women with suspected SGA pregnancies between 32+0 weeks gestation and 37+6 weeks gestation.

Methods
Women were randomised in a 3:1 ratio to biomarker-led care versus standard care. Biomarker tests were either revealed, with birth delayed until 40 weeks if normal (sFlt-1/PlGF < 38 pg/mL) and considered from 37 weeks if abnormal (sFlt-1/PlGF ≥ 38 pg/mL), or concealed alongside standard care.

Main Outcome Measures
Primary outcome was the feasibility of the study measured through the recruitment rate and adherence. Secondary outcomes were the qualitative, proof-of-concept and economic analyses.

Results
Out of 128 women invited to participate 78 women were recruited giving a recruitment rate of 60.1% (95% confidence interval 52%–69%). Sixty-seven of the 78 women consented to randomisation. Sixteen parents and 12 clinicians were interviewed. Fourty parents completed a questionnaire. Participants, partners and clinicians viewed the study as acceptable but experienced challenges in participation and delivering the study. There were no significant adverse events or differences in neonatal outcomes. Collection of health economics data was feasible.

Conclusions
The clinical, qualitative and economic results support the acceptability of utilising sFlt-1/PlGF to refine SGA management after 32+0 weeks but the feasibility is less certain.

Item Type: Article
Uncontrolled Keywords: PLANES study group; FGR; PlGF; SGA; angiogenic; biomarker; feasibility; late growth restriction; management; randomised; sFlt‐1; 3215 Reproductive Medicine; 32 Biomedical and Clinical Sciences; Contraception/Reproduction; Infant Mortality; Perinatal Period - Conditions Originating in Perinatal Period; Clinical Trials and Supportive Activities; Women's Health; Patient Safety; Pediatric Research Initiative; Clinical Research; Pregnancy; Reproductive health and childbirth; 3 Good Health and Well Being; 11 Medical and Health Sciences; Obstetrics & Reproductive Medicine; 3215 Reproductive medicine
Subjects: R Medicine > RG Gynecology and obstetrics
Divisions: Psychology (from Sep 2019)
Publisher: Wiley
Date of acceptance: 21 November 2025
Date of first compliant Open Access: 6 February 2026
Date Deposited: 06 Feb 2026 09:23
Last Modified: 06 Feb 2026 09:23
DOI or ID number: 10.1111/1471-0528.70106
URI: https://researchonline.ljmu.ac.uk/id/eprint/28059
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