Skip to content

Use of Pessary in Case of Cervical Insufficiency and Short Cervix

Use of Pessary in Case of Cervical Insufficiency and Short Cervix

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03096691
Enrollment
2
Registered
2017-03-30
Start date
2016-02-01
Completion date
2017-03-30
Last updated
2017-03-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preterm Labor

Keywords

cervical pessary, preterm labor, Cervical insufficiency

Brief summary

Prematurity is the most important cause of obstetric morbidity and mortality. Health centers and obstetricians are trying to reduce the preterm birth rate by taking into account the permanent effects of premature birth on human life in the early and long term. The most effective solution of preterm delivery is to determine the patients entering the risk group and to prevent preterm labor by putting the correct diagnosis at the right time. Recently, there have been studies on the efficacy of pessary practice in preventing preterm birth, but with the positive results of these studies, there has been hope for early birth prevention as well as other treatments. The aim of this study is; To assess the effectiveness of pessary use in patients with high risk for preterm labor and prophylactic cervical length less than 25 mm below 25 weeks and with a history of cervical insufficiency.

Detailed description

The aim of this study is; To assess the effectiveness of pessary use in patients with high risk for preterm labor and prophylactic cervical length less than 25 mm below 25 weeks and with a history of cervical insufficiency. 100 pregnant women with a preterm delivery history and / or a cervical length of less than 25 mm will be included among the pregnancies between 16 and 24 weeks of gestation referred to obstetric and perinatology clinics. Information will be given about the success of treatment in the prevention of early birth of the pessary and the use of the disease pessary. Urine culture and cervical culture samples will be taken from both groups of patients. In the presence of infection, the patient's treatment will be planned and out of work. If no infection is detected and the patient agrees to use the pessary, the pessary will be used to prevent premature birth.

Interventions

Silicone rings known as arabin pessary are used to support the cervix in women with a sonographic short cervix.

Sponsors

Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

100 pregnant women with a preterm delivery history and / or a cervical length of less than 25 mm will be included among the pregnancies between 16 and 24 weeks of gestation referred to obstetric and perinatology clinics. Information about the use of disease pessaries and treatment success in preventing premature birth of the pessary will be provided. Urine culture and cervical culture samples will be taken from both groups of patients. In the presence of infection, the patient's treatment will be planned and out of work. If no infection is detected and the patient agrees to use the pessary, the pessary will be used to prevent premature birth.

Eligibility

Sex/Gender
FEMALE
Age
17 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients with a cervical length of 25 mm\> and a preterm labor history in the previous pregnancy

Exclusion criteria

* Patients with vaginal bleeding, with congenital anomalies, chorioamnionitis

Design outcomes

Primary

MeasureTime frameDescription
Preterm deliveryLess than 34 weeks gestationSpontaneous delivery before 34 completed weeks

Countries

Turkey (Türkiye)

Contacts

Primary Contactdilsad herkiloglu, MD
dilsadherkiloglu@hotmail.com5428423742

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026