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Progesterone to Prevent Preterm Delivery

Primary Purpose

Preterm Birth

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Dydrogesterone Oral Tablet
Placebo Oral Tablet
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Preterm Birth

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • All women age ≥ 18 years old
  • Confirmed intrauterine singleton pregnancy
  • Gestational age less than 14 completed weeks as defined by pelvic ultrasound

Exclusion Criteria:

  • Silent miscarriage: mean gestational sac diameter ≥25 mm without fetal pole, or embryo with crown rump length ≥7 mm and no heartbeat, or no interval growth
  • Suspected ectopic pregnancy
  • Multiple pregnancy with silent miscarriage of one twin
  • Heavy vaginal bleeding requiring surgical intervention
  • Severe abdominal pain requiring surgical intervention
  • Presence of fever
  • History of adverse reaction to progesterone
  • History of breast or genital tract malignancy
  • History of suspected thromboembolic disease
  • Congenital uterine anomaly
  • Unwillingness or inability to comply with study procedures
  • Known paternal or maternal abnormal karyotype

Sites / Locations

  • Department of Obstetrics and GynaecologyRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Intervention group

Placebo group

Arm Description

Outcomes

Primary Outcome Measures

Rate of preterm delivery

Secondary Outcome Measures

Full Information

First Posted
February 4, 2018
Last Updated
April 8, 2019
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT03428685
Brief Title
Progesterone to Prevent Preterm Delivery
Official Title
A Double Blinded Randomized Controlled Trial of Early Use of Oral Progesterone in All Women for Prevention of Preterm Delivery in Singleton Pregnancy (SINPRO Study)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 15, 2019 (Actual)
Primary Completion Date
January 2021 (Anticipated)
Study Completion Date
January 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
Preterm birth (PTB) is a major challenge to perinatal health. It is defined as delivery before 37 completed gestational weeks. It accounts for 75% of perinatal deaths and more than 50% of long-term neurological disabilities, and it is the second most common cause of death in children under the age of 5 year. Neonates born preterm are at risk of respiratory distress syndrome, chronic lung disease, retinopathy of prematurity, necrotizing enterocolitis, intraventricular haemorrhage and sepsis in the short term, as well as cerebral palsy, motor and sensory impairment, learning difficulties, and increased risk of chronic disease in long run. It is estimated that the societal cost of PTB is $26 billion annually in the USA alone. Until now, prevention or reduction of PTB is based on identification of risk factors in obstetrical history, biochemical markers and short cervix. History of PTB and asymptomatic short cervix at the second trimester are both strong predictors for PTB. In women with asymptomatic short cervix at the second trimester, vaginal progesterone could effectively reduce PTB. Universal cervical length screening followed by treatment with vaginal progesterone has been shown to be the most cost effective strategy in preventing PTB. These findings were confirmed in meta-analysis. Nevertheless, only minority of women may benefit from progesterone treatment if it was being started at the second trimester. There is still a large proportion of PTB, which is currently not preventable, and the current approach to prevent PTB is far from ideal. One possible hypothesis is that the initiation of progesterone treatment would be too late for its effect to take place. Therefore, we decide to use oral progesterone in the current study. The objective of the study is to determine whether early use of progesterone can prevent PTB better when compared with universal screening of cervical length and followed by treatment with progesterone in those with short cervix.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Preterm Birth

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1714 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention group
Arm Type
Active Comparator
Arm Title
Placebo group
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Dydrogesterone Oral Tablet
Intervention Description
Oral dysdrogesteone 10mg tds will be prescribed from 12 - 36+6 weeks.
Intervention Type
Drug
Intervention Name(s)
Placebo Oral Tablet
Intervention Description
Placebos will be prescribed from 12 - 36+6 weeks.
Primary Outcome Measure Information:
Title
Rate of preterm delivery
Time Frame
before 37+0 gestational weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All women age ≥ 18 years old Confirmed intrauterine singleton pregnancy Gestational age less than 14 completed weeks as defined by pelvic ultrasound Exclusion Criteria: Silent miscarriage: mean gestational sac diameter ≥25 mm without fetal pole, or embryo with crown rump length ≥7 mm and no heartbeat, or no interval growth Suspected ectopic pregnancy Multiple pregnancy with silent miscarriage of one twin Heavy vaginal bleeding requiring surgical intervention Severe abdominal pain requiring surgical intervention Presence of fever History of adverse reaction to progesterone History of breast or genital tract malignancy History of suspected thromboembolic disease Congenital uterine anomaly Unwillingness or inability to comply with study procedures Known paternal or maternal abnormal karyotype
Facility Information:
Facility Name
Department of Obstetrics and Gynaecology
City
Hong Kong
State/Province
Hong Kong
ZIP/Postal Code
852
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ka Wang Cheung
Phone
(852) 22553111
Email
kelvincheung82@hotmail.com

12. IPD Sharing Statement

Citations:
PubMed Identifier
32000820
Citation
Cheung KW, Seto MTY, Ng EHY. Early universal use of oral progesterone for prevention of preterm births in singleton pregnancy (SINPRO study): protocol of a multicenter, randomized, double-blind, placebo-controlled trial. Trials. 2020 Jan 30;21(1):121. doi: 10.1186/s13063-020-4067-z.
Results Reference
derived

Learn more about this trial

Progesterone to Prevent Preterm Delivery

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