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NCT01207401 · ClinicalTrials.gov registry record · NA
Paracervical Block Before Intrauterine Device (IUD) Insertion
A NA study, sponsored by Northwestern University.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT01207401: Completed NA study, sponsored by Northwestern University.
NCT01207401 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 50 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.
The verdict
NCT01207401, a NA study, has completed, sponsored by Northwestern University.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate if a paracervical block containing 1% lidocaine administered prior to IUD insertion reduces insertion pain. The hypothesis is that women receiving paracervical analgesia will experience less pain during IUD insertion than those who do not receive such analgesia.
Primary Outcome
We asked participants to report their pain score on visual analogue scale (0mm=no pain and 100mm=worse pain possible) at the following time points: 1. Speculum placement 2. Tenaculum placement 3. Paracervical block administration(if subject is in this arm) 4. IUD insertion 5. Five minutes post procedure
Interventions
- DRUG Lidocaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2010-07 |
| Est. Completion | 2011-02 |
| Phase | NA |
What the finished NCT01207401 record still lists
NCT01207401 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 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 1 intervention - of which Lidocaine is the first listed.
NCT01207401 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01207401 about?
NCT01207401 is a clinical study titled "Paracervical Block Before Intrauterine Device (IUD) Insertion". The purpose of this study is to evaluate if a paracervical block containing 1% lidocaine administered prior to IUD insertion reduces insertion pain. The hypothesis is that women receiving paracervical analgesia will experience less pain during IUD insertion than those who do not receive such analges...
What is the current status of trial NCT01207401?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2010-07. Estimated completion is 2011-02.
What interventions are being tested in trial NCT01207401?
The interventions under investigation include: Lidocaine (DRUG).
Who is sponsoring clinical trial NCT01207401?
This trial is sponsored by Northwestern University, which has 1,209 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01207401's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 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
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