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

NCT01001897 · ClinicalTrials.gov registry record · NA

Use of Misoprostol for Intrauterine Device (IUD) Insertion in Nulliparous Women

A NA study, sponsored by University of Arizona.

Completed
Registry status
NA
Development phase
61
Enrollment target

NCT01001897: Completed NA study, sponsored by University of Arizona.

NCT01001897 is a NA study that has completed, run by University of Arizona. The registered enrollment target is 61 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01001897, a NA study, has completed, sponsored by University of Arizona.

COMPLETED
Registry status
NA
Development phase
61 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate if the use of misoprostol can make it easier for a provider, and less painful for a woman, to place an IUD if she has never had a child before.

Interventions

  • DRUG Placebo
  • DRUG Misoprostol

Trial Details

FieldValue
Enrollment Target 61 participants
Start Date 2009-10
Est. Completion 2011-04
Phase NA
University of Arizona

349 total trials

What the finished NCT01001897 record still lists

NCT01001897 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 61 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT01001897 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01001897 about?

NCT01001897 is a clinical study titled "Use of Misoprostol for Intrauterine Device (IUD) Insertion in Nulliparous Women". The purpose of this study is to evaluate if the use of misoprostol can make it easier for a provider, and less painful for a woman, to place an IUD if she has never had a child before.

What is the current status of trial NCT01001897?

This trial is currently completed. It is a NA study. The enrollment target is 61 participants. The study started on 2009-10. Estimated completion is 2011-04.

What interventions are being tested in trial NCT01001897?

The interventions under investigation include: Placebo (DRUG), Misoprostol (DRUG).

Who is sponsoring clinical trial NCT01001897?

This trial is sponsored by University of Arizona, which has 349 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01001897's enrollment target sits among peer trials

61 1164th of 2000 higher than 837 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04115306 · 61 participants · Phase 1

    Phase 1/1b/2 Study of Oral PMD-026 in Patients With Metastatic Breast Cancer

  • NCT05070845 · 61 participants · Phase 2

    Safety and Efficacy Study of PF-06835375 in Primary Immune Thrombocytopenia

  • NCT05187832 · 61 participants · Phase 1

    A Study of AND019 in Women With ER Positive HER2 Negative Advanced or Metastatic Breast Cancer

  • NCT05269316 · 61 participants · Phase 1

    Study to Evaluate IMP9064 as a Monotherapy or in Combination in Patients With Advanced Solid Tumors

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01001897, the US trial registry maintained by the National Library of Medicine. NCT01001897 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.