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NCT06158932 · ClinicalTrials.gov registry record · NA
A Single Group Study to Evaluate the Effects of a Myo-Inositol and D-Chiro Inositol Supplement on Symptoms Associated With Polycystic Ovary Syndrome and Hormone Imbalance
A NA study of Polycystic Ovary Syndrome and Hormone Imbalance, sponsored by Optify.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 1
- Study location
NCT06158932: Completed NA study of Polycystic Ovary Syndrome and Hormone Imbalance, sponsored by Optify.
NCT06158932 is a NA study of Polycystic Ovary Syndrome and Hormone Imbalance that has completed, run by Optify. The registered enrollment target is 40 participants, below the 17,257-participant average among 30 other Polycystic Ovary Syndrome trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06158932, a NA study of Polycystic Ovary Syndrome and Hormone Imbalance, has completed, sponsored by Optify.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a virtual single group study that will last 12 weeks. 40 female participants will take 4 capsules of the Optify Myo Inositol and D-Chiro Inositol Plus Folate and Vitamin D supplement per day. Questionnaires will be completed at Baseline, Week 4, Week 8 and Week 12. Participants will also provide a waist circumference measurement at Baseline and Week 12.
Primary Outcome
Measured via study-specific questionnaires with participants reporting menstrual cycle occurrence and regularity during the trial.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Optify Myo Inositol and D-Chiro Inositol Plus Folate and Vitamin D supplement
Study Locations (1)
California
- Citruslabs - Santa Monica
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2023-09-08 |
| Est. Completion | 2024-01-06 |
| Phase | NA |
What the finished NCT06158932 record still lists
NCT06158932 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 17,257-participant average among 30 other Polycystic Ovary Syndrome trials with a reported enrollment target (100% lower).
The record links to 2 conditions, with Polycystic Ovary Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Optify Myo Inositol and D-Chiro Inositol Plus Folate and Vitamin D supplement is the first listed.
NCT06158932 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT06158932 about?
NCT06158932 is a clinical study titled "A Single Group Study to Evaluate the Effects of a Myo-Inositol and D-Chiro Inositol Supplement on Symptoms Associated With Polycystic Ovary Syndrome and Hormone Imbalance". This is a virtual single group study that will last 12 weeks. 40 female participants will take 4 capsules of the Optify Myo Inositol and D-Chiro Inositol Plus Folate and Vitamin D supplement per day. Questionnaires will be completed at Baseline, Week 4, Week 8 and Week 12. Participants will also pro...
What is the current status of trial NCT06158932?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2023-09-08. Estimated completion is 2024-01-06.
What conditions does trial NCT06158932 study?
This clinical trial studies the following conditions: Polycystic Ovary Syndrome, Hormone Imbalance.
What interventions are being tested in trial NCT06158932?
The interventions under investigation include: Optify Myo Inositol and D-Chiro Inositol Plus Folate and Vitamin D supplement (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT06158932?
This trial is sponsored by Optify, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06158932 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT06158932's enrollment target sits among peer trials
40 20th of 30 higher than 10 of 30 other Polycystic Ovary Syndrome trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Polycystic Ovary Syndrome trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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