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NCT05676476Recruiting

The ACHIEVE Trial: Achieving Longer Gestation in Preeclampsia Via Antihypertensive Therapy.

Source: ClinicalTrials.gov · Last updated 12 Dec 2025

Brief summary (registry, in English)

The Achieve Trial is a randomized clinical trial to test whether lowering blood pressure to less than 140/90 mmHg in women with hypertensive disorders of pregnancy will prolong pregnancy.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
132 (estimated)
First submitted
3 Jan 2023
Start date
14 Feb 2023
Primary completion date
Dec 2026
Lead sponsor
University of Alabama at Birmingham
NCT number
NCT05676476

What you commit to

  • Study type: Interventional
  • Planned participants: 132
  • From 14 Feb 2023 to the primary completion date, Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Systolic blood pressure of 160 mm Hg or more, or diastolic blood pressure of 110 mm Hg or more on two occasions at least 4 hours apart (unless antihypertensive therapy is initiated before this time)
  • Impaired liver function that is not accounted for by alternative diagnoses and as indicated by abnormally elevated blood concentrations of liver enzymes (to more than twice the upper limit normal concentrations), or by severe persistent right upper quadrant or epigastric pain unresponsive to medications
  • New-onset headache unresponsive to medication and not accounted for by alternative diagnoses
  • Fetal growth restriction (lower than 10th percentile) at enrollment, based on an ultrasound within 3 weeks prior to enrollment
  • Oligohydramnios defined by amniotic fluid deepest vertical pocket \<2 cm based on an ultrasound within the 48 hours prior to enrollment

Other illness

  • Stage 2 chronic hypertension

Lab values

  • Thrombocytopenia defined as: lower than 100 x 10e9 platelets/L
  • Renal insufficiency (serum creatinine concentration more than 1.1 mg/dL or a doubling of the serum creatinine concentration in the absence of other renal disease)
  • Underlying renal dysfunction defined as, presenting the following parameters prior to 20 weeks gestation: baseline creatinine, equal to or higher than, 1.2 mg/dL Or proteinuria: defined as presenting protein in urine, equal to or higher than, 300 mg/24 hours or protein/creatinine ratio, equal to or higher than, 0.3 or Urine dipstick reading of greater than or equal to 2 at baseline and in the absence of a urinary tract infection

Other

  • Preeclampsia with severe features, defined per ACOG as:
  • Pulmonary edema
  • Visual disturbances
  • Contraindications to labetalol and nifedipine XL according to the FDA package insert
  • Patient unable to or unwilling to adhere to management recommendations
  • Fetal Reasons for Study Ineligibility:
  • Known major structural or chromosomal abnormality

Who the study is looking for

  • Pregnant women
  • Gestational age: 23 weeks, 0 days to 35 weeks, 6 days
  • Hypertensive disorder of pregnancy including gestational hypertension or preeclampsia, the non-severe form at enrollment, which is called without severe features by the American College of Obstetricians and Gynecologists.
  • No evidence of the severe form of preeclampsia, termed severe features, as outlined in maternal exclusions
  • No indication for delivery at the time of enrollment.
  • Planned expectant management at time of enrollment
  • Singleton or dichorionic twin gestation, defined at and beyond 14 weeks gestation. (A pregnancy complicated by a vanishing twin in the first trimester defined as less than 14 weeks gestation will be eligible.)
  • Intact membranes

Age in the registry: 14 years to 49 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alabama at Birmingham
Coordinator of this site? Confirm its status
BirminghamUnited StatesRecruiting
Oschner
Coordinator of this site? Confirm its status
New OrleansUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.