Paracetamol to minimize pain during second trimester amniocentesis

Phase 1

• Conditions: pregnancy GA 18- 22 wk who came to amniocentesissingleton pregnancyno underlying disease; paracetamol, pain, amniocentesis

• Registration Number: TCTR20141127003
• Lead Sponsor: ampang Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-11-27
• Study Completion: 2015-05-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Enrolling by invitation
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

pregnancy women GA 18-22 wk who came to amniocentesis
singleton pregnancy
no underlying disease

Exclusion Criteria

History of paracetamol allergy
Multiple pregnancy
Previous amniocentesis in this pregnancy
Denial for the study
More than one puncture of needle

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
pain score 30 minute VAS score

Secondary Outcome Measures

Name	Time	Method
A NA NA