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NCT03058978 · ClinicalTrials.gov registry record
Assessing Ovarian Function During Prolonged Implant Use
A clinical trial, sponsored by Planned Parenthood of the St. Louis Region and Southwest Missouri.
- Completed
- Registry status
- 117
- Enrollment target
NCT03058978 is a clinical trial that has completed, run by Planned Parenthood of the St. Louis Region and Southwest Missouri. The registered enrollment target is 117 participants.
The verdict
NCT03058978 has completed, sponsored by Planned Parenthood of the St. Louis Region and Southwest Missouri.
- COMPLETED
- Registry status
- 117 participants
- Enrollment target
Study Summary
The study will evaluate how the ovaries may be functioning while using the the Implanon®/Nexplanon® during the three years beyond the FDA approved duration. Ovarian function will be assessed with weekly serum progesterone levels. Participants will undergo weekly venipuncture for a total of four draws. Participants will be followed for 30 days.
Interventions
- DEVICE Etonogestrel Implant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 117 participants |
| Start Date | 2017-03-01 |
| Est. Completion | 2021-12-30 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03058978
The ClinicalTrials.gov registry entry for NCT03058978 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 117 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Planned Parenthood of the St. Louis Region and Southwest Missouri, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Etonogestrel Implant is the first listed.
NCT03058978 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03058978 about?
NCT03058978 is a clinical study titled "Assessing Ovarian Function During Prolonged Implant Use". The study will evaluate how the ovaries may be functioning while using the the Implanon®/Nexplanon® during the three years beyond the FDA approved duration. Ovarian function will be assessed with weekly serum progesterone levels. Participants will undergo weekly venipuncture for a total of four draw...
What is the current status of trial NCT03058978?
This trial is currently completed. The enrollment target is 117 participants. The study started on 2017-03-01. Estimated completion is 2021-12-30.
What interventions are being tested in trial NCT03058978?
The interventions under investigation include: Etonogestrel Implant (DEVICE).
Who is sponsoring clinical trial NCT03058978?
This trial is sponsored by Planned Parenthood of the St. Louis Region and Southwest Missouri, which has 3 total clinical trials registered on ClinicalTrials.gov.
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