Clinical Trials Logo

Clinical Trial Summary

This randomized controlled trial, compares perioperative and postoperative pain score by using visual analog scale in pregnant women undergoing amniocentesis. The experimental group will be given oral paracetamol premedication whereas the controlled group will be given oral placebo premedication.


Clinical Trial Description

Perioperative and postoperative amniocentesis are often painful which cause concerns to those who has to undergo amniocentesis. Anxiety is one of the factor that may prolong operative time, resulting in an increase risk of complication from the procedure. Furthermore, pregnant women, in order to relief the pain, might require others drugs, which has both maternal and fetal side effect. So In conclusion, this study aims to compare efficacy of oral paracetamol premedication and oral placebo premedication by using visual analog scale to evaluate pain. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03035045
Study type Interventional
Source Rajavithi Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date November 2016
Completion date July 2017

See also
  Status Clinical Trial Phase
Recruiting NCT04491149 - Study on the Ability of Virtual Reality Glasses in Anxiety and Pain Reduction in 50 Women Undergoing Amniocentesis or Feticide N/A