Effectiveness and acceptability of lidocaine spray in reducing perineal pain during spontaneous vaginal delivery: randomised controlled trial.

OBJECTIVES

To evaluate the effectiveness and acceptability of a lidocaine spray in reducing perineal pain during spontaneous vaginal delivery.

DESIGN

Randomised controlled trial.

SETTING

Consultant led obstetric unit.

PARTICIPANTS

185 women who had a spontaneous vaginal delivery without epidural analgesia.

INTERVENTIONS

Topically applied local anaesthetic spray (93 women) and placebo spray (92 women).

MAIN OUTCOME MEASURE

Primary outcome measure was pain during delivery (0-100 scale). The 16 secondary outcome measures included second degree perineal trauma during delivery, trauma of the genital tract, and dyspareunia by two months.

RESULTS

Lidocaine spray did not reduce pain during spontaneous vaginal delivery: mean 77 and 72 on a scale of 0-100 in the lidocaine and placebo groups, respectively (difference between means 4.8, 95% confidence interval -1.7 to 11.2). Lidocaine spray may reduce genital tract trauma during delivery, in particular second degree perineal trauma. The intervention was highly acceptable to the women and midwives.

CONCLUSIONS

Although lidocaine spray applied to the perineum during spontaneous vaginal delivery did not reduce perineal pain, it was acceptable to both the women and the midwives.

TRIAL REGISTRATION

Current controlled trials ISRCTN99732966 [controlled-trials.com].