68
Participants
Start Date
June 1, 2025
Primary Completion Date
June 30, 2027
Study Completion Date
June 30, 2028
Buffered Lidocaine
To determine if a 20 cc buffered (2 cc of sodium bicarbonate, 18 cc of 1% lidocaine) lidocaine paracervical block decreases pain with IUD placement in nulliparous women
Lidocaine 1% Injectable Solution
To determine if the unbuffered 1% lidocaine paracervical block offers any less pain control with IUD placement for nulliparous women
University of California, San Diego
OTHER