Ovarian Reserve in Intensive Care Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-35
SponsorHaseki Training and Research Hospital

About this trial

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.

Eligibility criteria

Qualifiers

18-35 years of age

Female patients followed in the intensive care unit for more than 24 hours for internal or surgical reasons,

Women whose ovarian reserve is being evaluated,

Disqualifiers

Previous ovarian surgery, endometriosis, endometrioma,

History of chemotherapy, radiotherapy,

Ovarian cyst, malignancy and other ovarian pathologies,

Women with single ovary,

Trial design

Treatments tested in this trial

  • Glaskow coma scala, The Acute Physiology and Chronic Health Evaluation System- APACHE, Injury Severity Score- ISS)

Treatment groups

75 Participants
are divided into 3 treatment groups

Locations

This trial has no locations