Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06999291

Ovarian Reserve in Intensive Care Patients

Evaluation of Ovarian Reserve in Critically Ill Patients Followed in the Intensive Care Unit

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
75 (estimated)
Sponsor
Haseki Training and Research Hospital · Academic / Other
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Not accepted

Summary

Gastrointestinal, pulmonary, nephrological, cardiac, neurologic and psychological effects in critically ill patients followed in the intensive care unit have been shown in the literature. However, the effects on ovarian reserve in these patients have not been sufficiently investigated and studies investigating this issue are limited in the literature. The synthesis, release frequency and amplitude of reproductive hormones change under stress. In addition, changes in ovarian homeostasis affect ovarian reserve. The aim of this study was to evaluate ovarian reserve in critically ill patients followed up in the intensive care unit.

Conditions

Interventions

TypeNameDescription
BEHAVIORALGlaskow coma scala, The Acute Physiology and Chronic Health Evaluation System- APACHE, Injury Severity Score- ISS)The uterus, endometrium and ovarian characteristics, endometrial thickness, ovarian follicle number and ovarian volume parameters, hormone panel (FSH, LH, E2, AMH), cortisol, prolactin and thyroid function tests routinely examined for ovarian reserve will be evaluated in the study.

Timeline

Start date
2025-06-15
Primary completion
2025-07-15
Completion
2025-11-15
First posted
2025-05-31
Last updated
2025-05-31

Source: ClinicalTrials.gov record NCT06999291. Inclusion in this directory is not an endorsement.