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Angiogenic Factors in the Conservative Management of Gestational Hypertension

Use of Angiogenic Factors in the Conservative Management of Gestational Hypertension. Prospective, Randomised, Controlled Study.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06123377
Enrollment
150
Registered
2023-11-08
Start date
2024-06-01
Completion date
2026-09-30
Last updated
2025-08-26

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

Conditions

Gestational Hypertension

Keywords

Gestational hypertension, Angiogenic factors

Brief summary

Hypertensive disorders of pregnancy (HPT) are an important cause of maternal-feto-neonatal morbidity and mortality, being one of the three leading causes of maternal death in our country and in developing countries. The only cure for THE is termination of pregnancy, which ends up being a decision in which gestational age and maternal risks must be balanced. Angiogenic factors have come to occupy an indispensable place in the arsenal of tools that can be used to separate the patient with a high likelihood of complications from those in whom prolongation of pregnancy could represent an important neonatal benefit. One of the most controversial scenarios is gestational hypertension, a group of hypertensive disorders considered the mildest form of the pre-eclamptic spectrum, where current recommendations indicate termination of pregnancy at 37 weeks. However, the decision is based on outdated guidelines developed at a time when angiogenic factors were just beginning to be known. The purpose of the study is to use angiogenic factors as a guide to decide the most appropriate gestational age for termination of pregnancy in patients diagnosed with gestational hypertension.

Interventions

DIAGNOSTIC_TESTAngiogenic factor

sFLt-1/PGIF below or equal to 33

Sponsors

Saint Thomas Hospital, Panama
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pregnant women between 24 and 40 weeks of gestation. * Diagnosis of Gestational Hypertension based on ACOG criteria * index sFlt-1/PIGF equal or below 33

Exclusion criteria

* Multiple gestation * Maternal vasculitis * Previous cesarean section (3 or more) * Neurological conditions * Chronic renal disease * Purpura * Heart disease * Index sFlt-1/PIGF of 34 or more

Design outcomes

Primary

MeasureTime frameDescription
Progression to preeclampsiaFrom the moment of randomization up until delivery. Between 1 and 17 weeks.In subject with gestational hypertension and sFlt-1/PIGF at enrollment equal or below 33, the appearance of proteinuria, severe criteria or sFlt-1/PIGF above 34

Secondary

MeasureTime frameDescription
Maternal / fetal morbidityUp until discharge. On average, 7 daysPresence of any/several indicators of maternal or fetal morbidity (abruptio placenta, HELLP syndrome, eclampsia, fetal growth restriction, acute lung edema).
Neonatal morbidityUp until discharge. On average, 3 daysPresence of any/several indicators of neonatal morbidity (Apgar scores, admission to NICU, encephalopatic hypoxia)

Countries

Panama

Contacts

Primary ContactOsvaldo Reyes, MD
oreyespanama@yahoo.es+507 65655041
Backup ContactGerado Cardenas, MD
drgacardenas@hotmial.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026