1207401
Last Update Posted: 2013-06-10
Recruiting has ended
Females accepted | 18 Years-50 Years |
50 Estimated Participants | No Expanded Access |
Interventional Study | Accepts healthy volunteers |
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 analgesia.
Eligibility
Relevant conditions:
Pain Control for Intrauterine Device Insertions
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the trial if you think are close to fitting criteria.
locations
Contact Information
Overall Contact
No valid contacts available
Data sourced from ClinicalTrials.gov