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Reproductive and Mental Health of Patients With Aplastic Anemia

A Study on Reproductive and Psychological Health in Aplastic Anemia Patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06936930
Enrollment
600
Registered
2025-04-20
Start date
2025-03-03
Completion date
2027-12-31
Last updated
2025-08-05

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

Conditions

Aplastic Anemia, Reproductive Health

Keywords

Aplastic Anemia

Brief summary

Aplastic anemia (AA) is a hematological disease characterized by bone marrow failure, leading to varying degrees of anemia, leukopenia, and thrombocytopenia. With the advancement of immunosuppressive therapy and hematopoietic stem cell transplantation, the survival of AA patients has significantly improved. However, these treatment approaches may result in reproductive system impairment. Reproductive health has been a major concern among reproductive-age AA patients. In female patients, it often manifests as irregular menstruation, amenorrhea, and infertility; while in male patients, it may present as reduced sperm count and low sperm motility. The reproductive impairment observed in AA patients may be attributed to various factors, including the disease's underlying pathophysiology, side effects of used medications such as androgens and the toxicity conditioning agents during transplantation. Notably, immunosuppressive agents (such as cyclosporine and antithymocyte globulin) and chemotherapeutic drugs (such as cyclophosphamide) can suppress hematopoiesis and directly damage the gonads, thereby impairing reproductive function. Furthermore, long-term use of these medications may disrupt the endocrine system, affecting the secretion of sex hormones and overall reproductive capacity. Additionally, chronic anemia in AA patients can lead to compensatory physiological changes in other body systems, which may also indirectly affect reproductive health.

Interventions

OTHERSex hormone monitoring

Sex hormone monitoring includes the concentrations of follicle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol (E2), progesterone (P), prolactin (PRL), and testosterone (T).

Sponsors

Institute of Hematology & Blood Diseases Hospital, China
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years

Inclusion criteria

* Diagnosis of AA * Male or female, aged 18-40 years * ECOG performance status ≤2 * Willing and able to comply with the requirements for this study and written informed consent

Exclusion criteria

* Diagnosis of inherited bone marrow failure syndromes * Combined with other hematological diseases * Chemotherapy-induced bone marrow failure * Pregnant or breastfeeding women * Subjects with a history of mental illness or severe psychological disorders * Subjects with a history of reproductive system cancer (eg, penile cancer, testicular cancer, prostate cancer, ovarian cancer, cervical cancer, vaginal cancer, etc.) * Subjects that the investigator believes have other reasons that make them unsuitable for inclusion in this study

Design outcomes

Primary

MeasureTime frameDescription
Proportion of patients with abnormal sex hormone levelsBaseline, 6 months post-treatment, 12 months post-treatmentThe concentrations of FSH, LH, E2, P, PRL and T.

Secondary

MeasureTime frameDescription
Stress levelsBaselinePerceived Stress Scale (PSS-10) can range from 0 to 40 with higher scores indicating higher perceived stress.
Depression symptomsBaselinePatient Health Questionnaire (PHQ-9) can range from 0 to 27 with higher scores indicating greater severity of depression.
Social supportBaselineMedical outcomes study social support survey (MOS-SSS) can range from 0 to 100 with higher scores indicate greater perceived social support.

Countries

China

Contacts

Primary ContactJingyu Zhao, MPH
zhaojingyu@ihcams.ac.cn13752253515

Outcome results

None listed

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