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Clinical Trial Summary

This randomized control trial aim to evaluate the effectiveness of local lidocaine spray application to the cervix on the reducing of pain score during the manual vacuum aspiration


Clinical Trial Description

This is a double blinded, placebo controlled study which compose of two arms. The treatment group is the local lidocaine spray application to the cervix with the intravenous opioid. The control group is the the intravenous opioid with the placebo (normal saline) before the manual vacuum aspiration. The outcome is to compare the visual analog pain score during and after procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06344637
Study type Interventional
Source UdonThani Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date December 14, 2023
Completion date July 30, 2024

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