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Cervical pessary versus vaginal progesterone in women with a singleton pregnancy, a short cervix, and no history of spontaneous preterm birth at less than 34 weeks gestation: open label, multicentre, randomised, controlled trial

Objective To compare the effectiveness of cervical pessary and vaginal progesterone in the prevention of adverse perinatal outcomes and preterm birth in pregnant women of singletons with no prior spontaneous preterm birth at less than 34 weeks’ gestation and who have a short cervix of 35 mm or less. Design Open label, multicentre, randomised, controlled trial. Setting 20 hospitals and five obstetric ultrasound practices in the Netherlands. Participants Women with a healthy singleton pregnancy and an asymptomatic short cervix of 35 mm or less between 18 and 22 weeks’ gestation were eligible. Exclusion criteria were prior spontaneous preterm birth at less than 34 weeks, a cerclage in situ, maternal age of younger than 18 years, major congenital abnormalities, prior participation in this trial, vaginal blood loss, contractions, cervical length of less than 2 mm or cervical dilatation of 3 cm or more. Sample size was set at 628 participants. Interventions 1:1 randomisation to an Ar

GHTC statement for WHA HHS Stakeholder Listening Session on clinical trials resolution

GHTC participated and shared a statement at the US Department of Health and Human Services (HHS) Stakeholder Listening Session in preparation for the 76th World Health Assembly on implementation of last year s resolution on strengthening clinical trials.

Evidence for Safety, Efficacy of Analgesics for Acute Low Back Pain Is Limited

The safety and efficacy of analgesics for acute low back pain remain uncertain; clinicians should use caution when prescribing these medicines.

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