Pharmacological Preparation of the Cervix for Hysteroscopy

Status Completed

Clinical Trial Summary

Pain accompanying office hysteroscopy is the most common reason for its discontinuation. Urogenital atrophy may cause technical difficulties in passage through the cervical canal, further increasing the pain. The aim was to evaluate the effectiveness of vaginal estradiol and hyaluronic acid to facilitate diagnostic hysteroscopy in peri- and postmenopausal women.

Clinical Trial Description

A prospective cohort tertiary-center study includes women over 45 years of age subjected to office hysteroscopy in 2021-2022. Women who consent are assigned to three study arms: i) estradiol 0.5 mg in vaginal cream twice daily for 10 days pre-procedure, ii) hyaluronic acid 5 mg in vaginal gel twice daily for 10 days pre-procedure, iii) no treatment (control). The following endpoints are compared: need for cervical dilation, incidence of severe urogenital atrophy and vaso-vagal reaction, time of cervical passage, cervical canal diameter, pain during and after the procedure in the Numeric Rating Scale (NRS). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05783479
Study type	Interventional
Source	Jagiellonian University
Contact
Status	Completed
Phase	N/A
Start date	June 1, 2022
Completion date	January 31, 2023

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