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Impact of N-acetylcysteine (NAC) supplementation in pregnancies with pre eclampsia

N-acetylcysteine ??supplementation in pregnant women with pre-eclampsia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
REBEC
Registry ID
RBR-6n5p6gw
Enrollment
Unknown
Registered
2024-11-06
Start date
2021-06-21
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Pre-eclampsia

Interventions

This is a randomized, placebo-controlled, double-blind clinical study. Experimental group: 60 women supplemented with capsules containing 600 mg of N-acetylcysteine ??(NAC), once a day, after a main m

Sponsors

Universidade Federal de Alagoas
Lead Sponsor
Hospital Universitário Professor Alberto Antunes
Collaborator

Eligibility

Sex/Gender
Female
Age
11 Years to No maximum

Inclusion criteria

Inclusion criteria: Women; adolescents and adults; between 24 and 28 weeks of gestation; diagnosed with pre-eclampsia; attended prenatal care at the Professor Alberto Antunes University Hospital

Exclusion criteria

Exclusion criteria: Multiple pregnancies; women with neurological disorders and comorbidities that may influence the outcomes of pregnancy (diabetes mellitus, cardiovascular problems, urinary tract infection, kidney disease, autoimmune diseases, hepatitis, syphilis, human immunodeficiency virus, among others); as well as pregnant women who are alcoholics; smokers; those who use antioxidant and/or anti-inflammatory drugs; pregnant women whose newborns have serious malformations (cardiac, renal or hepatic) or genetic syndromes diagnosed during prenatal care

Design outcomes

Primary

MeasureTime frame
It is expected to find improvements in perinatal outcomes, such as birth weight and length

Secondary

MeasureTime frame
Assess biomarkers of redox imbalance and inflammation

Countries

Brazil

Contacts

Public ContactAlane Oliveira

Universidade Federal de Alagoas

alanecabral@gmail.com+55(82) 987331950

Outcome results

None listed

Source: REBEC (via WHO ICTRP)