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The effect of Oral High Energy Nutritional Supplements on appetite, pregnancy and fetal outcomes in underweight women during their first pregnancy

Effect of high energy nutritional supplements on appetite regulators, energy intake and lipid profile in underweight primigravida

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10088578
Enrollment
24
Registered
2018-03-27
Start date
2018-04-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Low weight in women who are pregnant for the first time Pregnancy and Childbirth Malnutrition in pregnancy

Interventions

After participants are recruited, written informed consent and a detailed medical history will be taken to exclude chronic illness, eating disorders, and major gastrointestinal operations. Each partic

Sponsors

Khyber medical university
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Healthy 2. First pregnancy 3. Body mass index <18.5 kg/m2 4. Aged 15-45 years

Exclusion criteria

Exclusion criteria: 1. Major illness such as gestational diabetes mellitus, pregnancy-induced hypertension, thyroid disease or liver disease 2. Previously on any long-term medication. 3. Allergic to supplement ingredients. 4. Previous history of gastrointestinal tract anomalies, surgeries and any other eating disorders e.g. bulimia nervosa, anorexia nervosa and purging disorders

Design outcomes

Primary

MeasureTime frame
1. Energy consumed during the days prior to experimental trial and during ad libitum breakfast and lunch calculated using dietary analysis software (Windiets 2005, The Robert Gordon University, Aberdeen, Scotland, UK) 2. Appetite measured using a validated appetite questionnaire at baseline, week 16 and postnatally 3. Lipid profile analyzed using Cobas C3 analyzer 4. Maternal hemoglobin, hematocrit and mean corpuscular volume measured by hematology analyzer at baseline, week 16 & potnatal visit 5. Pregnancy outcome 6. Iron, zinc and calcium levels in cord blood analyzed by atomic absorption spectrometry (AAS) 7. Iron, zinc and calcium levels in colostrum measured by Cobas 8000 Modular Analyzer

Secondary

MeasureTime frame
1. Maternal satisfaction and compliance 2. Socioeconomic data

Countries

Pakistan

Contacts

Public ContactKalsoom Tariq

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 10, 2026