Lidocaine-Prilocaine Cream in Conjunction With Paracervical Block for Pain With Abortion

Withdrawn before enrolling · Phase 3 · Has a placebo group

Conditions studied: Pain

In brief

The investigators theorize that the application of a lidocaine-prilocaine cream 5-10 minutes prior to the administration of a paracervical block could decrease pain associated with its administration and pain with abortion overall.

Key facts

Study ID

NCT03508804

Run by

Stanford University

People needed

0

Starts

2020-12-01

Expected to finish

2022-12-01

Last updated by the study team

2018-05-16

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• surgical abortion patient at 5 0/7 to 11 6/7 weeks gestational age;
• English or Spanish speaking;
• ability to give informed consent

You may not qualify if…

• pre-operative use of misoprostol;
• allergy to study medications (lidocaine, prilocaine, versed, fentanyl);
• known uterine anomaly;
• prior cervical surgery

Where it is running

• Stanford Health Care — Stanford, California, United States

Full record on ClinicalTrials.gov

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