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NCT06999291

Ovarian Reserve in Intensive Care Patients

Not yet recruiting Last updated 31 May 2025
What this trial tests

trial testing Glaskow coma scala, The Acute Physiology and Chronic Health Evaluation System- APACHE, Injury Severity Score- ISS) in Anti-Mullerian Hormone Deficiency in 75 participants. Not yet recruiting.

Timeline
15 June 2025
Primary endpoint
15 July 2025
15 November 2025

Quick facts

Lead sponsorHaseki Training and Research Hospital
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment75
Start date15 June 2025
Primary completion15 July 2025
Estimated completion15 November 2025

Drugs / interventions tested

Conditions studied

Sponsor

Haseki Training and Research Hospital

Who can join

Adults 18 to 35, female only, with Anti-Mullerian Hormone Deficiency. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Anti-Mullerian Hormone Deficiency

Currently open trials in the same condition.

Other Haseki Training and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06999291.

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