Novel topical formulation of lidocaine provides significant pain relief for intrauterine device insertion Pharmacokinetic evaluation and randomized placebo controlled trial

A topically applied, short-acting, viscous solution of lidocaine provides highly significant pain relief for women undergoing insertion of an IUD, and no safety concerns are apparent.

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Authors

Sara Tornblom-Paulander, M.D., Berith K. Tingåker, M.D., Ph.D., Agneta Werner, M.D., Caroline Liliecreutz, M.D., Ph.D., Peter Conner, M.D., Ph.D., Hans Wessel, M.D., Ph.D., Gunvor Ekman-Ordeberg, M.D., Ph.D.

Volume 103, Issue 2, Pages 422-427

Abstract

Objective:

To investigate the pharmacokinetics, safety, and analgesic efficacy of a novel topical formulation of lidocaine at insertion of an intrauterine device (IUD).

Design:

Randomized controlled trial; phase-I and phase-II studies.

Setting:

University and public hospitals.

Patient(s):

Women aged ≥18 years who wanted to receive an IUD. Four women were parous in phase I; all in phase II were nulliparous.

Intervention(s):

A single, 8.5-mL dose of lidocaine formulation (SHACT) was administered (to the portio, cervix, and uterus) with a specially designed applicator.

Main Outcome Measure(s):

The phase-I study (single-arm) was designed for pharmacokinetic assessment; the phase-II study (randomized) was intended for investigation of efficacy and safety.

Result(s):

From the phase-I study (15 participants), mean pharmacokinetic values were: maximum plasma concentration: 351 ± 205 ng/mL; time taken to reach maximum concentration: 68 ± 41 minutes; and area under the concentration–time curve from 0 to 180 minutes: 717 ± 421 ng*h/mL. Pain relief was observed with lidocaine vs. placebo in the phase-II study (218 women, randomized). Mean visual analog scale score for maximum pain during the first 10 minutes after IUD insertion was 36% lower with lidocaine than with placebo (28.3 ± 24.6 vs. 44.2 ± 26.0). Pain intensity was also significantly lower in the lidocaine group at 30 minutes. On average, 3 of 4 patients will have less pain with lidocaine than with placebo. Adverse events were similar in the placebo and lidocaine groups. No serious adverse events were reported.

Conclusion(s):

Lidocaine provides pain relief lasting for 30–60 minutes for women undergoing IUD insertion, without any safety concerns. Further studies of this lidocaine formulation, for IUD insertion and other clinical applications, are planned.

Clinical Trial Registration Number:

2011-005660-18 and 2011-006220-20 (EudraCT).

Read the full text at: http://www.fertstert.org/article/S0015-0282(14)02286-9/fulltext


Fertility and Sterility

Editorial Office, American Society for Reproductive Medicine

Fertility and Sterility® is an international journal for obstetricians, gynecologists, reproductive endocrinologists, urologists, basic scientists and others who treat and investigate problems of infertility and human reproductive disorders. The journal publishes juried original scientific articles in clinical and laboratory research relevant to reproductive endocrinology, urology, andrology, physiology, immunology, genetics, contraception, and menopause. Fertility and Sterility® encourages and supports meaningful basic and clinical research, and facilitates and promotes excellence in professional education, in the field of reproductive medicine.

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