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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.
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
| Field | Value |
|---|---|
| Enrollment Target | 306 participants |
| Start Date | 2021-02-17 |
| Est. Completion | 2024-03-15 |
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Full Details on ClinicalTrials.gov ↗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.
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