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Higher dose cervical 2% lidocaine gel for IUD insertion: a randomized controlled trial
Rebecca H Allen1, Christina Raker, Vinita Goyal
1Department of Obstetrics and Gynecology, Warren Alpert Medical School of Brown University, Women and Infants Hospital, Providence, RI 02905, USA.
Topical 2% lidocaine cervical gel did not significantly reduce pain during intrauterine device (IUD) insertion for first-time users. The study found no difference in pain scores compared to placebo, indicating limited effectiveness for this procedure.
Area of Science:
- Obstetrics and Gynecology
- Pain Management
- Clinical Trials
Background:
- Intrauterine device (IUD) insertion is a common gynecological procedure.
- Pain experienced during IUD insertion can be a barrier to uptake.
- Effective pain management strategies are needed to improve patient experience.
Purpose of the Study:
- To evaluate the efficacy of 6 mL of 2% lidocaine cervical gel in mitigating pain during IUD insertion.
- To compare pain levels between women receiving lidocaine gel and those receiving a placebo.
Main Methods:
- A randomized, double-blind, placebo-controlled trial was conducted.
- Participants were first-time IUD users receiving either 2% lidocaine gel or placebo.
- Pain was assessed using a 0-100 mm visual analog scale.
Main Results:
- No significant difference in pain scores was observed between the lidocaine and placebo groups for speculum insertion, tenaculum placement, or IUD insertion.
- Mean pain scores for IUD insertion were 35.2 in the lidocaine group and 36.7 in the placebo group (p=.8).
Conclusions:
- Topical 2% lidocaine cervical gel is not effective in reducing pain associated with tenaculum placement and IUD insertion.
- Further research may be needed to explore alternative or adjunct pain relief methods for IUD insertion.
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