RecruitingPhase 4NCT06433453

Three Dimensional Ultrasonographic Detection of Human Ovulation

Three Dimensional Ultrasonographic Detection of Human Ovulation and Anovulation


Sponsor

University of Saskatchewan

Enrollment

30 participants

Start Date

Apr 22, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The research aims to compare diagnosis of ovulation and anovulation in 2D and 3D ultrasonography.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 40 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Finger prick blood test, a drug called Indomethacin 50 MG, and others for people with ovulation disorder. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 40 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGIndomethacin 50 MG

The medication is commenced when a preovulatory follicle is observed. It will be administered for a minimum of one day, up to a maximum of 7 days. It will be discontinued when anovulation is observed.

PROCEDURETransvaginal ultrasound scans

Ultrasound scans done intermittently before and after an ovulatory or anovulatory event

DIAGNOSTIC_TESTFinger prick blood test

Capillary blood extracted from a finger prick. Blood spots are collected on a specialized card, dried and frozen before reproductive hormones are assayed from them.

DIAGNOSTIC_TESTUrine test

Early morning urine tests to assay reproductive hormones


Locations(1)

Department of Obstetrics, Gynecology and Reproductive Sciences, University of Saskatchewan

Saskatoon, Saskatchewan, Canada

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NCT06433453


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