Paracervical Versus Intracervical Lidocaine

NACompletedINTERVENTIONAL
Enrollment

89

Participants

Timeline

Start Date

December 31, 2007

Primary Completion Date

February 29, 2008

Study Completion Date

February 29, 2008

Conditions
Abortion, InducedPain
Interventions
PROCEDURE

Paracervical block

The paracervical block was administered using 20 ml of buffered lidocaine and a 5/8 inch, 25-gauge needle. A small amount was injected at the tenaculum site, and the remainder equally distributed around the cervicovaginal junction at 3, 5, 7, and 9 o'clock. The depth was standardized at 5/8 inch by inserting the needle to the hub.

PROCEDURE

Intracervical

The intracervical block was administered using 20 ml of buffered lidocaine and a 1-1/2 inch, 20 gauge needle in order to overcome the increased resistance to injection caused by the cervical stroma. A small amount was injected at the tenaculum site, and the remainder into the cervical stroma at 12, 3, 6, and 9 o'clock, at a depth of 1-1/2 inch by inserting the needle to the hub.

DRUG

Buffered Lidocaine, vasopressin, sodium bicarbonate

The buffered lidocaine preparation for both block techniques consisted of 50 mL of 1% lidocaine, 5 units of vasopressin, and 5 mL 8% sodium bicarbonate.

Trial Locations (1)

92101

Planned Parenthood, San Diego

All Listed Sponsors
lead

University of California, San Diego

OTHER

NCT00816751 - Paracervical Versus Intracervical Lidocaine | Biotech Hunter | Biotech Hunter