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Ovulation clinical trials

View clinical trials related to Ovulation.

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NCT ID: NCT05448378 Completed - Insulin Clinical Trials

Evaluation of D-chiro-inositol Treatments

Start date: June 4, 2022
Phase: N/A
Study type: Interventional

Healthy women will take tablets containing 600 mg D-chiro-inositol twice per day for one month. We will evaluate metabolic and hormonal.parameters, as insulienmia, glycemia, estradiol, testosterone.

NCT ID: NCT04382001 Completed - Ovulation Clinical Trials

Heart Rate Variability During the Menstrual Cycle

Start date: June 1, 2020
Phase:
Study type: Observational

In this study, women will be required to wear a chest heart rate monitor and wrist heart rate monitor daily and collect daily early morning urine samples for the duration of one complete menstrual cycle. This will enable comparisons between data collected from the heart rate monitor and hormone analysis in urine samples to be made.

NCT ID: NCT04008277 Completed - Ovulation Clinical Trials

Investigation of Heart Rate Variability During the Menstrual Cycle

Start date: July 19, 2019
Phase:
Study type: Observational

In this study, women will be required to wear a heart rate monitor continuously and collect daily early morning urine samples for the duration of one complete menstrual cycle. This will enable comparisons between data collected from the heart rate monitor and hormone analysis in urine samples to be made.

NCT ID: NCT03778099 Completed - Clinical trials for Polycystic Ovary Syndrome

The Effect of Cinnamon on Ovulation Induction in Women With Polycystic Ovary Syndrome

PCOS
Start date: September 20, 2018
Phase: Phase 3
Study type: Interventional

Title: The effect of cinnamon supplementation on ovulation induction in women with polycystic ovary syndrome, Jeddah 2019: Randomized Double-Blind Placebo-controlled trial Phase: III Population: 118 women with polycystic ovary syndrome will be recruited from Obstetrics and Gynecology clinics in King Abdul-Aziz University Hospital, Jeddah 2019. Subject Participation Duration: Each participant will be followed for three months. Intervention: 2g of cinnamon capsules daily will be provided. Objectives: Primary Objective: 1. To compare the effectiveness of cinnamon supplement in combination with clomiphene citrate versus clomiphene citrate alone on ovulation in women with PCOS, in King Abdul-Aziz University Hospital in Jeddah 2019. 2. To measure the difference in insulin resistance after three months of cinnamon supplementation in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019. 3. To determine the effect of cinnamon and CC on menstrual cyclicity, approximated by menstrual frequency, during the study period, in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019 4. To evaluate the quality of life in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019. Secondary Objectives: - To measure the pregnancy rate in women with PCOS in King Abdul-Aziz University Hospital, Jeddah 2019 Description of Study Design: The participants will be randomized in 1:1 fashion. Allocation concealment will be ensured using similar bottles labeled by letters A and B, to receive either the combination of cinnamon supplement and clomiphene citrate or clomiphene citrate with placebo. First visit: Patients will be evaluated during the early follicular phase for progesterone level and HOMA-IR and QUICK-I. Follow up: 3 months. Last Visit: Patients will be re-evaluated to compare the difference.

NCT ID: NCT01802060 Completed - Ovulation Clinical Trials

Accuracy of SPD Persona LH Assay When Compared to Ultrasound Observed Ovulation and Other Indices of Ovulation

Start date: February 2013
Phase: N/A
Study type: Observational

This study will examine the performance of the Persona assays in identifying the time when risk of pregnancy is highest by comparing results to ultrasound observed ovulation and other indices of ovulation.

NCT ID: NCT01129245 Completed - Ovulation Clinical Trials

The Effect of a Non-hormonal Cox-2 Inhibitor (Celebrex) on Ovulation

Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect that Celebrex (a COX-2 inhibitor and non-steroidal anti-inflammatory drug) has on ovulation.

NCT ID: NCT00796133 Completed - Ovulation Clinical Trials

A Phase 2, Dose-finding, Cross-over Study to Evaluate the Effect of a NES/E2 Transdermal Gel Delivery on Ovulation Suppression in Normal Ovulating Women

Start date: November 2008
Phase: Phase 2
Study type: Interventional

This is a Phase 2, dose-finding, cross-over study for the purposes of evaluating the effect of a NES/E2 transdermal gel delivery on ovulation suppression in normal ovulating women.

NCT ID: NCT00254189 Completed - Ovulation Clinical Trials

Study Evaluating Effects of Levonorgestrel and Ethinyl Estradiol on Ovulation

Start date: December 2002
Phase: Phase 2
Study type: Interventional

To determine the ability of a monophasic oral contraceptives ("OC") regimen of Levonorgestrel ("LNG") 90 mg and Ethinyl Estradiol ("EE") 20 mg to inhibit ovulation during 84 days of continuous therapy.