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NCT Number: NCT06354439

Use of Letrozole for Ectopic Pregnancy

A randomized clinical trial using oral letrozole 10mg/day for 7 days, for treating early cases of ectopic pregnancy, compared to intramuscular methotrexate

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 4

Primary location

About this study

This is a multicenter randomized clinical trial on the use of letrozole in the medical treatment of tubal ectopic pregnancy. Tubal ectopic pregnancy is an abnormal pregnancy in the fallopian tube. They occurred in about 8% of all pregnancies presenting to the emergency department. Methotrexate (MTX), administered systemically (intramuscularly), is a widely used medication for the treatment of unruptured tubal ectopic pregnancies and has been recommended as first-line treatment for early cases of ectopic pregnancy.

Letrozole is an aromatase inhibitor and can suppress estradiol levels. Some recent studies have shown that its use can be applied in cases of ectopic pregnancy.

The aim of this non-inferiority clinical trial is to verify that letrozole treatment is non-inferior to methotrexate treatment in women with early ectopic pregnancy who are hemodynamically stable.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • Diagnosis of ectopic pregnancy
  • Desire for reproduction
  • Ease of return
  • Undetermined pregnancy location with abnormal hCG growth
  • Presence of a heterogeneous adnexal mass on pelvic ultrasound suggestive of a tubal ectopic pregnancy with an hCG level ≤ 3000 mIU/ml
  • Absence of fetal cardiac activity
  • Average diameter of the adnexal mass ≤ 3.5 cm
  • Hemodynamically stable
  • No significant abdominal pain (i.e, < 6 on a visual analog scale)

Exclusion criteria

  • Presence of a significant amount of free fluid in the pelvis (as assessed by the ultrasound technician)
  • Allergy to methotrexate or letrozole
  • A reduction in β-hCG ≥ 50% in 2 measurements with 48 hours between them or

≥ 85% in 4 days, or ≥ 95% in 7 days before randomization

  • Abnormal liver function test (Alanine transaminase (ALT) ≥ 2 times the upper limit of normal)
  • Abnormal renal function test (glomerular filtration rate ≤ 45 ml/min)
  • Hemoglobin <10 g/dl
  • Platelets <120.000/ml
  • Presence of heterotopic pregnancy
  • Do not wish to participate in the study.

Treatment and study plan

Letrozole tablets

Drug

10 mg of letrozole PO for 7 days

Other names: letrozole 2,5mg - 4 tables

Methotrexate Sodium

Drug

100 mg of methotrexate IM, single dose

Other names: methotrexate intramuscular (IM)

Primary outcomes

  1. levels of beta fraction of human chorionic gonadotropin (beta-hCG)

    Time frame: weekly after the first day of intervention until reaching levels of beta-hCG below 5 milli-International unit per milliliter (assessed up to 5 months)"

    On day 4 (D4) and 7(D7), beta-hCG levels will be measured. If a reduction equal or above 15% between D4 and D7 were observed, serum beta-hCG will be measured until reach levels < 5 milli-International unit per milliliter (mIU/ml).

Study contacts

Contact information is provided by the study sponsor or research team.

Ricardo F Savaris, MD, PhD

CONTACT

[email protected]

+55 51 997781966

Sponsors and collaborators

Lead sponsor

Hospital de Clinicas de Porto Alegre

Other

Registry information

Official study title

Use of Letrozole in the Treatment of Early Ectopic Pregnancy

Acronym: EcZOL

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Apr 9, 2024
Registry last updated
Apr 9, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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