This was a randomized controlled trial of 400 women who attended the outpatient clinic of Menoufia University Hospital for copper IUD insertion. The women were randomly assigned to cough and control groups.The primary outcome measure was the level of pain experienced at different steps of IUD insertion measured by a visual analogue scale (VAS).
Name: forced coughing
Description: The primary outcome measure was the level of pain experienced at different steps of IUD insertion measured by a visual analogue scale (VAS).
Measure: The level of pain experienced at different steps of IUD insertion measured by a visual analogue scale (VAS). Time: Up to 22 monthsAllocation: Randomized
Single Group Assignment
There is one SNP
The primary outcome measure was the level of pain experienced at different steps of IUD insertion measured by a visual analogue scale (VAS).. Inclusion Criteria: - Non pregnant women (aged 18-45 years) requesting copper T380A IUD insertion for contraception. --- T380A ---
A statistician not directly involved in the study prepared a computer generated randomization list and placed the allocation information in sequentially numbered sealed envelopes that were opened according to the attendance of the subjects after signing the informed consent Inclusion Criteria: - Non pregnant women (aged 18-45 years) requesting copper T380A IUD insertion for contraception. --- T380A ---
We recruited non pregnant women (aged 18-45 years) requesting copper T380A IUD insertion for contraception. --- T380A ---