Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04678817 · ClinicalTrials.gov registry record

Same Day Oral EC and Implant Initiation

A clinical trial, sponsored by University of Utah.

Completed
Registry status
306
Enrollment target

NCT04678817 is a clinical trial that has completed, run by University of Utah. The registered enrollment target is 306 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04678817 has completed, sponsored by University of Utah.

COMPLETED
Registry status
306 participants
Enrollment target

Study Summary

This is a study for clients presenting for emergency contraception (EC). EC is used to prevent pregnancy after unprotected intercourse. Clients presenting for EC may be offered either the copper or hormonal IUD or oral EC. Current guidelines allow for same-day implant initiation at the time of an EC encounter, as long as oral LNG EC is co-administered. This study will look at pregnancy rates and clients willingness to receive same-day implant + oral EC and same-day IUDs.

Interventions

  • DEVICE Etonogestrel contraceptive implant with oral levonorgestrel
  • DEVICE Levonorgestrel intrauterine device
  • DEVICE Copper T380A intrauterine device

Trial Details

FieldValue
Enrollment Target 306 participants
Start Date 2021-02-17
Est. Completion 2024-03-15

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT04678817

The ClinicalTrials.gov registry entry for NCT04678817 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 306 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Etonogestrel contraceptive implant with oral levonorgestrel is the first listed.

NCT04678817 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04678817 about?

NCT04678817 is a clinical study titled "Same Day Oral EC and Implant Initiation". This is a study for clients presenting for emergency contraception (EC). EC is used to prevent pregnancy after unprotected intercourse. Clients presenting for EC may be offered either the copper or hormonal IUD or oral EC. Current guidelines allow for same-day implant initiation at the time of an EC...

What is the current status of trial NCT04678817?

This trial is currently completed. The enrollment target is 306 participants. The study started on 2021-02-17. Estimated completion is 2024-03-15.

What interventions are being tested in trial NCT04678817?

The interventions under investigation include: Etonogestrel contraceptive implant with oral levonorgestrel (DEVICE), Levonorgestrel intrauterine device (DEVICE), Copper T380A intrauterine device (DEVICE).

Who is sponsoring clinical trial NCT04678817?

This trial is sponsored by University of Utah, which has 818 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.