Trials / Completed
CompletedNCT04638023
Arabin Pessary in Singleton Pregnancy
Arabin Pessary Use in Women at High Risk for Preterm Birth: 7 Years' Experience in a Single Tertiary Centre
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 58 (actual)
- Sponsor
- National University of Malaysia · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This was a retrospective study sharing the experience of women high risk for spontaneous preterm birth managed by Arabin pessary.
Detailed description
The study recruitment was from 1st January 2013 until 31st December 2019. Inclusion criteria were previous mid-trimester miscarriage and/or preterm birth, previous cervical surgery or short cervical length on routine ultrasound. The primary outcome measure was birth before 34 weeks gestation.
Conditions
- Previous Mid Trimester Miscarriage
- Previous Preterm Birth
- Previous Cervical Surgery
- Short Cervix on Ultrasound
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Arabin pessary | Arabin pessary was inserted intravaginally electively in women with cervical insufficiency (history based) or as emergency in those with short cervix on ultrasound. |
Timeline
- Start date
- 2017-01-01
- Primary completion
- 2018-01-01
- Completion
- 2018-01-01
- First posted
- 2020-11-20
- Last updated
- 2020-11-24
Locations
1 site across 1 country: Malaysia
Source: ClinicalTrials.gov record NCT04638023. Inclusion in this directory is not an endorsement.