J. Bartley et al., Double-blind randomized trial of mifepristone in combination with vaginal gemeprost or misoprostol for induction of abortion up to 63 days gestation, HUM REPR, 16(10), 2001, pp. 2098-2102
BACKGROUND: Gemeprost and misoprostol are two of the most widely used prost
aglandins in combination with mifepristone for medical abortion in early pr
egnancy. However, the efficacy and side-effects of those two drugs given va
ginally have not been assessed in a randomized trial. METHODS: Randomized d
ouble-blind controlled trial involving 999 women undergoing an abortion at
gestational age less than or equal to 63 days who received either 0.5 mg ge
meprost (group 1, n = 499) or 800 mug misoprostol (group II, n = 500) vagin
ally similar to 48 h after taking 200 mg mifepristone by mouth. The rate of
complete abortion and the side-effects were compared between the groups. R
ESULTS: A total of 89 cases was excluded from full analysis of outcome beca
use either they aborted after mifepristone alone (n = 2), had an ectopic pr
egnancy (n = 1), or because the outcome was uncertain as they failed to att
end their follow-up appointment (n = 86). The rate of complete abortion was
very high (> 95%) in both groups but significantly higher after treatment
with misoprostol than with gemeprost [436/453 (98.7%) versus 451/457 (96.2%
), P = 0.019, difference 2.5%, confidence interval 0.4-4.7%] and there were
fewer ongoing pregnancies (n = I versus n = 8, P < 0.018). Surgical interv
ention rose significantly with gestation in women who received gemeprost (P
< 0.03) but not with misoprostol. The incidence of side-effects such as di
arrhoea (13.7 versus 16.4%) and vomiting (27.8 versus 29.7%) was similar in
women who received misoprostol or gemeprost respectively, as was the durat
ion and amount of bleeding. CONCLUSIONS: (i) Both regimens using a reduced
dose of mifepristone are highly effective. methods of inducing abortion in
early pregnancy; (ii) vaginal misoprostol is the preferred prostaglandin be
cause it is it is associated with fewer failures than low-dose gemeprost, p
articularly at gestation greater than or equal to 49 days.