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Recruiting

NCT Number: NCT07116772

Serial Assessment of Fertility Experiences

The SAFE study is a long-term research project that watches people with sickle cell anemia (SCA) over time. The main goal is to see how a medicine called hydroxyurea affects their growth, puberty, and ability to have children. A second goal is to see how hydroxyurea affects pregnancy outcomes, by comparing people who take the medicine to those who don't.

Recruiting

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Key information

Age range

8 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Centro de Obstetricia y Ginecologia, Santo Domingo, Dominican Republic

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About this study

Hydroxyurea is a medicine that helps people with sickle cell anemia (SCA), a serious blood disease. It works by increasing a special type of hemoglobin (called fetal hemoglobin) that helps prevent sickle cell problems.

This medicine is especially helpful in places where it's hard to get safe blood transfusions. Studies from around the world have shown that hydroxyurea is safe and can reduce serious health problems caused by SCA (like pain, strokes, and lung issues). It can also help people with SCA live longer, healthier lives.

However, the investigators still don't know everything about how hydroxyurea affects long-term growth, puberty, fertility, or pregnancy; especially in areas with fewer medical resources.

To learn more, researchers are planning a large international study. They will follow people with SCA over time to see how hydroxyurea affects their development, ability to have children, and pregnancy outcomes. Participants will visit the clinic every few months for check-ups, blood tests, and other health assessments. Girls who have started their periods will take pregnancy tests every six months, and boys may be asked to provide a semen sample if they agree. Everyone will also answer questions about their health and fertility regularly.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with documented sickle cell anemia (SCA).
  • At least 8 years of age at the time of enrollment.
  • Enrolled on the EXTEND or SACRED study.
  • Provide informed consent.
  • Able to take part in all parts of the study, including treatments, check-ups, and follow-up visits.

Exclusion criteria

  • Currently taking part in another treatment study (not EXTEND or SACRED).
  • Has received other treatments for sickle cell disease in the past 6 months.

Treatment and study plan

Primary outcomes

  1. Clinical Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    The number of people who experience serious health events like pregnancy, stroke, cancer, or death.

Secondary outcomes

  1. Female Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Female fertility potential will be measured using serum anti-mullerian hormone (physiologic parameter)

  2. Female Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Female ability to conceive will be assessed using incidence of pregnancy (questionnaire)

  3. Female Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Outcomes of pregnancy will be categorized as either abortion or live birth (questionnaire)

  4. Female Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Mode of delivery will be categorized as vaginal or c-section (questionnaire)

  5. Female Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Prematurity of infant will be categorized as premature or full term (questionnaire)

  6. Female Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Weight of infant will be categorized as normal birth weight or low birth weight (questionnaire)

  7. Male Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Male fertility potential will be measured using sperm analysis (physiologic parameter)

  8. Male Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Male ability to conceive will be assessed using incidence of impregnated partner (questionnaire)

  9. Male Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Outcomes of pregnancy will be categorized as either abortion or live birth (questionnaire)

  10. Male Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Mode of delivery will be categorized as vaginal or c-section (questionnaire)

  11. Male Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Prematurity of infant will be categorized as premature or full term (questionnaire)

  12. Male Reproductive Potential and Outcomes

    Time frame: From enrollment up to 10 years after enrollment.

    Weight of infant will be categorized as normal birth weight or low birth weight (questionnaire)

Study contacts

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

Russell E Ware, MD, PhD

CONTACT

[email protected]

513-803-4597

Teresa Latham, DrPh

CONTACT

[email protected]

513-803-7822

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Collaborators

  • Centro de Obstetricia y Ginecologia Recruiting Santo Domingo, Dominican Republic
  • The University of The West Indies

Registry information

Official study title

A Prospective Longitudinal Study of Growth, Development, Fertility and Reproductive Outcomes Among Adolescents and Young Adults With Sickle Cell Anemia With Hydroxyurea

Acronym: SAFE

Important dates

Study start
2023
Primary completion
2035
Study completion
2035
First posted
Aug 12, 2025
Registry last updated
Feb 4, 2026

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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