Brody 2011.

Methods	Location: Chattanooga, TN, USA Recruitment time: August 2010 to September 2012 Sample size calculation and outcome of focus: no mention
Participants	General with N: 210 women Source: University department of obstetrics and gynecology Inclusion criteria: receiving Mirena for standard indications, did not receive NSAID Exclusion criteria: do not desire to be in study, have taken narcotics, Mirena not able to be placed, cervical dilation required, allergy to lidocaine
Interventions	1) 5 cc 2% lidocaine gel on cervix and intracervically 2) Lubricant: KY gel Timing: no mention
Outcomes	Primary: VAS (0 to 10) pain scores in 3 categories of 0 to 2, 3 to 4, and ≥ 5; assessed at time of insertion and at 5 and 10 min after insertion Secondary: no mention
Notes	IUC used: LNG‐IUS (Mirena) Estimated completion September 2012 Could not find any publication; unable to obtain information from investigator (15 October 2014)