Verify the Safety and Effectiveness of the Cerclage Pessary in Prevention and Treatment of High-risk Preterm Pregnancy

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorQH Medical Technology Ltd.

About this trial

Verify the safety and effectiveness of the cerclage pessary in the prevention and treatment of high-risk preterm pregnancy.

Eligibility criteria

Qualifiers

Women with a pregnancy and a history of at least one spontaneous preterm birth before 34+0 weeks and/or a history of late abortion

12+0 -18+0 weeks of gestation

Minimal age of 18 years

Informed consent signature

Disqualifiers

The previous preterm delivery is iatrogenic proterm labor

Major fetal abnormalities (requiring surgery or leading to infant death or severe handicap)

The pregnant woman with severe cervical erosion, cervical polyp, hemorrhage and the doctors think she could not use cerclage pessary

The pregnant woman with uterine cervicitis

Trial design

Treatments tested in this trial

  • Progesterone
  • pessary

Treatment groups

300 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators