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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: Completed study, sponsored by Planned Parenthood of the St. Louis Region and Southwest Missouri.

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

Primary Outcome

Comparisons of serum progesterone levels between BMI (kg/m\^2) categories will be made using ANOVA or Kruskal-WIllis depending on the normality of distribution.

Interventions

  • DEVICE Etonogestrel Implant

Trial Details

FieldValue
Enrollment Target 117 participants
Start Date 2017-03-01
Est. Completion 2021-12-30

What the finished NCT03058978 record still lists

NCT03058978 is an observational study that tracks outcomes without assigning an intervention. The registered 117 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 1 intervention - of which Etonogestrel Implant is the first listed.

NCT03058978 does not publish any study locations in the registry export this page uses.

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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Source: ClinicalTrials.gov NCT03058978, the US trial registry maintained by the National Library of Medicine. NCT03058978 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.