Clinical Trials Directory

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UnknownNCT03035045

Oral Paracetamol Premedication Effect on Maternal Pain in Amniocentesis

Oral Paracetamol Premedication Effect on Maternal Pain in Amniocentesis: A Randomized Double Blind Placebo-controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
240 (estimated)
Sponsor
Department of Medical Services Ministry of Public Health of Thailand · Other Government
Sex
Female
Age
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGParacetamol
DRUGPlacebo Oral Tablet

Timeline

Start date
2016-11-01
Primary completion
2017-06-01
Completion
2017-07-01
First posted
2017-01-27
Last updated
2017-01-27

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT03035045. Inclusion in this directory is not an endorsement.