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A Pilot RCT on the Management of Term Prelabour Rupture of Membranes

Primary Purpose

Prelabour Rupture of Membranes at Term

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Expectant management
Minimal Vaginal examinations (only when necessary)
Active management
Routine vaginal examinations
Sponsored by
University of Central Lancashire
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prelabour Rupture of Membranes at Term focused on measuring Prelabour rupture of membranes, term pregnancy, management, vaginal examination, induction of labour, expectant management

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Prelabour rupture of membranes (confirmed)
  • Term pregnancy - from 37+0 till 41+2 weeks gestation (both inclusive)
  • Normal/Low risk pregnancy
  • Singleton, cephalic pregnancy
  • No known current infectious diseases
  • Aged 18-45 years old
  • Understands English and is able to read and write in English
  • Agree for their placentas to be sent to histology if clinical signs of infection
  • Not taking part in other clinical research at present
  • Consent to take part

Exclusion criteria:

  • Pregnancy of 36+6 or less or 41+3 or more weeks gestation
  • Breech or oblique presentation
  • Twin or multiple pregnancy
  • Previous caesarean section
  • Meconium stained liquor
  • Pre-eclampsia
  • Diabetes
  • Known to be colonised by Group B streptococcus
  • Current infections: HIV, Hepatitis B, Herpes
  • Doesn't give consent for the placenta to be sent to histology if clinical signs of infection
  • Not able to understand, read or write in English
  • Currently taking part in other clinical research

Sites / Locations

  • Lancashire Teaching Hospitals NHS TrustRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Active Comparator

Arm Label

Expectant management and minimal vaginal examinations

Expectant management and routine vaginal examinations

Active management and minimal vaginal examinations

Active management and routine vaginal examinations

Arm Description

Expectant management up to approximately 96hours and vaginal examinations only when necessary during active labour

Expectant management up to approximately 96hours and routine vaginal examinations during active labour

Induction of labour at approximately 24hours and vaginal examinations only when necessary during active labour

Induction of labour at approximately 24hours and routine vaginal examinations

Outcomes

Primary Outcome Measures

Percentage of eligible women who agree to take part in the study

Secondary Outcome Measures

Percentage of participants who stay in the allocation arm
Percentage of participants who find the interventions acceptable
Acceptability of the interventions to participants as measured by the study questionnaire

Full Information

First Posted
July 14, 2016
Last Updated
November 14, 2016
Sponsor
University of Central Lancashire
Collaborators
Lancashire Care NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT02872883
Brief Title
A Pilot RCT on the Management of Term Prelabour Rupture of Membranes
Official Title
"Active vs Expectant Management and Routine vs Only-when-necessary Vaginal Examinations During Labour for Prelabour Rupture of Membranes at Term, a Pilot RCT Study"
Study Type
Interventional

2. Study Status

Record Verification Date
November 2016
Overall Recruitment Status
Unknown status
Study Start Date
November 2016 (undefined)
Primary Completion Date
October 2017 (Anticipated)
Study Completion Date
November 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Central Lancashire
Collaborators
Lancashire Care NHS Foundation Trust

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a pilot study that will eventually result in a main randomised controlled trial that will look at what management is associated with a higher rate of normal birth and a lower rate of chorioamnionitis (maternal infection) when women break their waters but labour does not start. Spontaneous rupture of the membranes (when the waters break) at term (37-42 weeks gestation) is a physiological event that happens during labour. However, according to Gunn et al. (1970) in 8-10 % of the cases the membranes rupture before labour starts. The time between the rupture and the onset of labour is called latent phase and time wise is variable. Studies have showed no statistically significant differences in terms of neonatal infection or chorioamnionitis when the investigators induce labour with prostaglandins compared to when labour starts spontaneously (Hannah et al 1996). Seaward et al. (1997) noted a number of confounding factors that might relate to the incidence of chorioamnionitis (maternal infection), the strongest predictor was having more than 8 vaginal examinations since the rupture of membranes and before delivery which was a stronger predictor than the duration of the latent phase. It is thought that by reducing the number of internal examinations, chorioamnionitis may be reduced, and hence neonatal infection may also be reduced. The main RCT will compare clinical outcomes and maternal satisfaction when women consent to be randomized to four groups: (1) Active management and routine internal examinations during labour, (2) Active management and reduced internal examinations, (3) Expectant management and routine internal examinations, (4) Expectant management and reduced internal examinations. This application seeks ethics approval for the pilot phase to ensure that a definitive study can be undertaken appropriately. It is important to test that all the components work well individually and as a whole, to estimate sample size and ultimately to test the integrity of the research protocol before embarking on the main trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prelabour Rupture of Membranes at Term
Keywords
Prelabour rupture of membranes, term pregnancy, management, vaginal examination, induction of labour, expectant management

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Expectant management and minimal vaginal examinations
Arm Type
Experimental
Arm Description
Expectant management up to approximately 96hours and vaginal examinations only when necessary during active labour
Arm Title
Expectant management and routine vaginal examinations
Arm Type
Experimental
Arm Description
Expectant management up to approximately 96hours and routine vaginal examinations during active labour
Arm Title
Active management and minimal vaginal examinations
Arm Type
Experimental
Arm Description
Induction of labour at approximately 24hours and vaginal examinations only when necessary during active labour
Arm Title
Active management and routine vaginal examinations
Arm Type
Active Comparator
Arm Description
Induction of labour at approximately 24hours and routine vaginal examinations
Intervention Type
Procedure
Intervention Name(s)
Expectant management
Intervention Type
Procedure
Intervention Name(s)
Minimal Vaginal examinations (only when necessary)
Intervention Type
Procedure
Intervention Name(s)
Active management
Intervention Type
Procedure
Intervention Name(s)
Routine vaginal examinations
Primary Outcome Measure Information:
Title
Percentage of eligible women who agree to take part in the study
Time Frame
12 months during pilot stage
Secondary Outcome Measure Information:
Title
Percentage of participants who stay in the allocation arm
Time Frame
12 months during pilot stage
Title
Percentage of participants who find the interventions acceptable
Description
Acceptability of the interventions to participants as measured by the study questionnaire
Time Frame
The questionnaire will be completed by the participants between 4-8 weeks after giving birth

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Prelabour rupture of membranes (confirmed) Term pregnancy - from 37+0 till 41+2 weeks gestation (both inclusive) Normal/Low risk pregnancy Singleton, cephalic pregnancy No known current infectious diseases Aged 18-45 years old Understands English and is able to read and write in English Agree for their placentas to be sent to histology if clinical signs of infection Not taking part in other clinical research at present Consent to take part Exclusion criteria: Pregnancy of 36+6 or less or 41+3 or more weeks gestation Breech or oblique presentation Twin or multiple pregnancy Previous caesarean section Meconium stained liquor Pre-eclampsia Diabetes Known to be colonised by Group B streptococcus Current infections: HIV, Hepatitis B, Herpes Doesn't give consent for the placenta to be sent to histology if clinical signs of infection Not able to understand, read or write in English Currently taking part in other clinical research
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lucia Ramirez-Montesinos, MSc BSc
Phone
00447897236172
Email
Lramirez-montesinos@uclan.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lucia Ramirez-Montesinos, MSc BSc
Organizational Affiliation
University of Central Lancashire
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Soo Downe, PhD MSc BSc
Organizational Affiliation
University of Central Lancashire
Official's Role
Study Director
Facility Information:
Facility Name
Lancashire Teaching Hospitals NHS Trust
City
Preston
State/Province
Lancashire
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ann Docherty, Research midwife
Email
ann.docherty@lthtr.nhs.uk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

A Pilot RCT on the Management of Term Prelabour Rupture of Membranes

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