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NCT06891794 · ClinicalTrials.gov registry record · NA
Use of Cervical Cap and Menstrual Disc for Application of Topical Anesthetic Prior to IUD Insertion
A NA study of IUD, sponsored by Oregon Health and Science University.
- Recruiting
- Registry status
- NA
- Development phase
- 24
- Enrollment target
- 1
- Study location
NCT06891794: Recruiting NA study of IUD, sponsored by Oregon Health and Science University.
NCT06891794 is a NA study of IUD that is actively recruiting participants, run by Oregon Health and Science University. The registered enrollment target is 24 participants, below the 247-participant average among 5 other IUD trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06891794, a NA study of IUD, is actively recruiting participants, sponsored by Oregon Health and Science University.
- RECRUITING
- Registry status
- NA
- Development phase
- 24 participants
- Enrollment target
- 1
- Study location
Study Summary
This prospective, open label, double arm, feasibility group study will recruit participants planning to undergo office intrauterine device (IUD) placement without sedation or anxiolysis at the Center for Women's Health. Participants will self-administer a topical anesthetic using a contraceptive cervical cap or menstrual disc. Twenty-four nulliparous women will be recruited to receive one of two administration methods immediately prior to IUD placement (12 subjects in each arm): 1) menstrual disc filled with 5g eutectic mixture of local anesthetics (EMLA) cream or 2) cervical cap filled with 5g EMLA cream.
Primary Outcome
The number of participants able to correctly place the cap or disc as instructed, assessed by provider
Conditions Studied
Interventions
- COMBINATION_PRODUCT Menstrual disc with EMLA cream
- COMBINATION_PRODUCT Cervical cap with EMLA cream
Study Locations (1)
Oregon
- Oregon Health & Science University - Portland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 24 participants |
| Start Date | 2025-08-04 |
| Est. Completion | 2026-04 |
| Phase | NA |
What NCT06891794 shows while recruiting
NCT06891794 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 24 participants, a relatively small participant target, below the 247-participant average among 5 other IUD trials with a reported enrollment target (90% lower).
The record links to 1 condition, with IUD appearing as the primary indexed condition, and to 2 interventions - of which Menstrual disc with EMLA cream is the first listed.
NCT06891794 reports a single indexed study location in Oregon.
Frequently Asked Questions
What is clinical trial NCT06891794 about?
NCT06891794 is a clinical study titled "Use of Cervical Cap and Menstrual Disc for Application of Topical Anesthetic Prior to IUD Insertion". This prospective, open label, double arm, feasibility group study will recruit participants planning to undergo office intrauterine device (IUD) placement without sedation or anxiolysis at the Center for Women's Health. Participants will self-administer a topical anesthetic using a contraceptive cer...
What is the current status of trial NCT06891794?
This trial is currently recruiting. It is a NA study. The enrollment target is 24 participants. The study started on 2025-08-04. Estimated completion is 2026-04.
What conditions does trial NCT06891794 study?
This clinical trial studies the following conditions: IUD.
What interventions are being tested in trial NCT06891794?
The interventions under investigation include: Menstrual disc with EMLA cream (COMBINATION_PRODUCT), Cervical cap with EMLA cream (COMBINATION_PRODUCT).
Who is sponsoring clinical trial NCT06891794?
This trial is sponsored by Oregon Health and Science University, which has 546 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06891794 being conducted?
This trial has 1 study location across Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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