Clinical Study

A Randomized Controlled Trial of Misoprostol and Sulprostone to End Pregnancy after Fetal Death

Table 4

Women’s assessment of the treatments and their side effects.

Outcome* MisoprostolSulprostone
( )( )
% %

Nausea
None4462.94159.4
All nausea2332.92539.1
Light,1420.01724.6
Moderate22.968.7
Severe710.022.9
Not reported34.334.3

Vomiting
None5071.44971.0
All vomiting1724.31724.6
Only once57.168.7
Several episodes1115.71115.9
Not reported45.734.3

Diarrhea
None5680.05681.2
All diarrhea1115.71014.5
Light,68.6710.1
Moderate45.711.4
Severe11.422.9
Not reported34.334.3

Pain score (range 0 to 10)
Median (interquartile range)5 (3–7)5 (2–7)

Women’s perception of the duration of induction
Too long1014.31420.3
Not too long2637.12637.7
Uncertain3144.32637.7
Not answered34.334.3

Women’s opinion on restriction of movement *
Felt no restriction4057.12231.9
Any restriction2434.34463.8
Some restriction2130.03652.2
Too restricted34.3811.6
Not answered68.634.3

Women’s opinion on the acceptability of the procedure
Very acceptable3448.62333.3
Acceptable2434.33956.5
Poor acceptability710.045.8
Not answered57.134.3

Women’s overall satisfaction
Very satisfied5071.45072.5
Satisfied1420.01115.9
Little or not at all22.934.3
Not answered45.757.2
Would have preferred the other method
Yes34.368.7
No3955.73043.5
Do not know2332.93043.5
Not answered57.134.3

*There was no statistical difference in outcome between the two groups except for restriction of movement (Chi square test; ).