To Evaluate the Efficacy of Flushing the Uterine Cavity With Lidocaine Before Hysterosalpingo-Foam Sonography to Reduce Procedure-related Pain Clinical Trial
Official title:
Analgesic Efficacy of Intrauterine Lidocaine Flushing in Hysterosalpingo-foam Sonography: A Double-blind Randomized Controlled Trial
To evaluate the efficacy of flushing the uterine cavity with lidocaine before Hysterosalpingo-Foam Sonography (HyFoSy) to reduce procedure-related pain.
This randomized, double-blind, placebo-controlled trial was approved by the institutional
ethics committee (# 0189-19; approval 22-09-2019) and written informed consent was obtained
from all participants. The sample was composed of women who were referred for tubal patency
evaluation as part of their fertility workup. Exclusion criteria were a known allergy to
lidocaine, unprotected intercourse, profuse vaginal bleeding and genital tract inflammation
or infections (e.g. pelvic inflammatory disease (PID) or suspected sexually transmitted
diseases (purulent vaginal discharge upon speculum insertion), salpingitis or tubo-ovarian
abscess), psychological or neurological lesions affecting sensation, prior cervical surgery,
cervical stenosis.
Randomization took place on the day of the procedure so that the staff had sufficient time to
prepare the instruments and the medication/placebo. Women were randomized into one of two
groups in a 1:1 ratio, using a predetermined randomization code, prepared by a research
nurse. They were allocated to receive either: (1) an intrauterine infusion of 2% lidocaine
(Rafa laboratories, Israel) ('lidocaine flushing' group), or (2) an intrauterine infusion of
0.9 % normal saline (placebo group) just prior to HyFoSy.
An assigned nurse prepared the medications according to the allocation group. Lidocaine and
normal saline were placed in identical 10-mL disposable syringes. The lidocaine solution as
well as the normal saline were both colorless and thus indistinguishable by the women and the
performing sonographer, all of whom were blind to the group assignment.
No form of premedication was given before HyFoSy. The exam was performed after complete
cessation of menstrual bleeding and before the 14th day of the ovulatory cycle. The women
were placed in the supine position on an examination couch and a baseline transvaginal scan
was performed by one of two experienced clinicians to detect any pelvic pathologies. A
vaginal speculum was introduced into the vagina for visualization of the cervix. The cervix
and vagina were cleansed with iodine solution. A balloon-less GIS catheter (GynaecologIQ)19
with a soft tapered tip was inserted into the endocervical canal for all HyFoSy procedures.
The use of a tenaculum for uterine traction or a cervical dilatator to introduce the catheter
was avoided in all cases. The speculum was then removed, taking care not to dislodge the
catheter, and the ultrasound transducer was introduced vaginally. The abovementioned phase of
the exam was performed by the same physician in all cases. The un-labelled solution (2%
lidocaine solution or normal saline) was instilled slowly into the uterine cavity through the
catheter until good distension and clear visualization of the uterine cavity was obtained.
The ExEm® Foam-kit was used to produce foam according to the manufacturer's instructions9.
The foam was then injected slowly via the GIS catheter under direct ultrasound guidance,
until its passage or non-passage through both fallopian tubes had been assessed. All
examinations were performed using a Samsung WS80A ultrasound system equipped with a V5-9 MHz
endovaginal probe.
Pain scores were obtained before the procedure to collect a baseline value and were
reassessed after the HyFoSy examination. All patients were asked to stay for 10-20 min in a
waiting area and were asked to score the level of pain they experienced during the procedure
on a visual analog scale (VAS) as described in20. The VAS consisted of a 10 cm line ranging
from 0 to 10 (anchored by 0=no pain and 10=very severe pain). Patients were asked to mark the
number that represented their perceived level of pain. Based on the VAS scores, the pain
level ratings were classified as: mild (rated 1-3), moderate (4-6) or severe (7-10).
Sample size was calculated to detect 1 unit of mean difference of pain score between the two
groups using the VAS, assuming that 1 was the SD (standard deviation) within the group.
Twenty-seven women were needed in each group to reject the null hypothesis of 0.05 with a
power of 0.9. Adding 30% to that number to compensate for any missing data gave a number of
39 women in each group.
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