Study of Local Anesthesia as a Method to Decrease IUD Insertion Related Pain

Withdrawn before enrolling · Phase 4 · Has a placebo group

Conditions studied: IUD Insertion Complication, Pain Control

In brief

Despite the high efficacy of intrauterine devices (IUDs), some women choose not to receive IUDs secondary to the pain associated with insertion. Nulliparous women may be especially susceptible to procedure-related pain from IUD insertion. This study will investigate the difference in perceived pain from IUD insertion, comparing local anesthesia to a placebo, among women who have not had a vaginal delivery before. The investigators anticipate that among women who have not had a previous vaginal delivery, the pain associated with IUD insertion will be significantly decreased after administration of local anesthesia.

Key facts

Study ID
NCT01967017
Run by
Johns Hopkins University
People needed
0
Starts
2014-06-01
Expected to finish
2014-06-01
Last updated by the study team
2017-06-12

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.