To examine whether application of lidocaine spray in cervical preparation for second trimester dilatation and evacuation alleviates pain and is superior to current protocol of preparation without analgesia and superior to placebo. a double- blind, randomized, placebo- controlled trial, performed at a single tertiary medical center. Eligible participants aged 18 and older and about to undergo dilation \& evacuation of the uterus between 12 to 24 weeks of gestation. Participants will be randomized using computer generated allocation to receive 10% Xylocaine (lidocaine group) spray or normal saline 0.9% (placebo group), applied identically topically to the endocervix and ectocervix before laminaria insertion. The primary outcome will be the participant's reported pain score immediately after the first laminaria was inserted as measured on a 10 cm visual analog scale (VAS). Secondary outcomes wiil be reported pain scores at speculum removal, 15 minutes after speculum insertion and immediately before the D\&E procedure.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
134
will local application of lidocaine to the cervix alleviate pain of laminaria insertion
Sheba Medical Center
Ramat Gan, Israel
Pain immediately after inserton of first laminaria
Women's reported VAS pain score immediately after the insertion of the first laminaria.
Time frame: immediately after first laminaria insertion
Reported pain afer speculum removal, 15 minutes after speculum inserion and before D&E
Reported VAS pain at speculum removal, 15 minutes after speculum insertion and before D\&E
Time frame: After speculum removal, 15 minutes after speculum insertion and before D&E
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.