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NCT02219308 · ClinicalTrials.gov registry record · NA

Pain Control for Intrauterine Device Placement Using Paracervical Block

A NA study of Pain Due to Intrauterine Contraceptive Device, sponsored by University of California, San Diego.

Completed
Registry status
NA
Development phase
67
Enrollment target
2
Study locations

NCT02219308 is a NA study of Pain Due to Intrauterine Contraceptive Device that has completed, run by University of California, San Diego. The registered enrollment target is 67 participants. The trial reports 2 study locations across 1 state.

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The verdict

NCT02219308, a NA study of Pain Due to Intrauterine Contraceptive Device, has completed, sponsored by University of California, San Diego.

COMPLETED
Registry status
NA
Development phase
67 participants
Enrollment target
2
Study locations

Study Summary

Intrauterine device (IUD) placement can be painful for patients during and after the procedure. Fear of pain from IUD insertion can be a barrier to obtaining this highly effective long acting reversible contraception. Currently there are no proven effective methods for reduction of pain during and after placement of modern IUDs. Paracervical block pain may decrease this placement pain.

Interventions

  • PROCEDURE Paracervical Block (PCB)
  • PROCEDURE No Paracervical Block (Sham PCB)

Study Locations (2)

California

  • UCSD - San Diego
  • Planned Parenthood Mission Bay Parker Center - San Diego

Trial Details

FieldValue
Enrollment Target 67 participants
Start Date 2014-10
Est. Completion 2017-10
Phase NA

Sponsor

University of California, San Diego

775 total trials

What the Registry Record Tells You About NCT02219308

The ClinicalTrials.gov registry entry for NCT02219308 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Diego, which has 775 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Pain Due to Intrauterine Contraceptive Device appearing as the primary indexed condition, and to 2 interventions - of which Paracervical Block (PCB) is the first listed.

NCT02219308 reports 2 study locations spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT02219308 about?

NCT02219308 is a clinical study titled "Pain Control for Intrauterine Device Placement Using Paracervical Block". Intrauterine device (IUD) placement can be painful for patients during and after the procedure. Fear of pain from IUD insertion can be a barrier to obtaining this highly effective long acting reversible contraception. Currently there are no proven effective methods for reduction of pain during and a...

What is the current status of trial NCT02219308?

This trial is currently completed. It is a NA study. The enrollment target is 67 participants. The study started on 2014-10. Estimated completion is 2017-10.

What conditions does trial NCT02219308 study?

This clinical trial studies the following conditions: Pain Due to Intrauterine Contraceptive Device.

What interventions are being tested in trial NCT02219308?

The interventions under investigation include: Paracervical Block (PCB) (PROCEDURE), No Paracervical Block (Sham PCB) (PROCEDURE).

Who is sponsoring clinical trial NCT02219308?

This trial is sponsored by University of California, San Diego, which has 775 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02219308 being conducted?

This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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.