ACTRN12615000445572
Terminated
Phase 3
For women in labour for the first time does a partograph with a graduated dystocia line compared to a standard sloping action line increase the likelihood of a spontaneous vaginal birth: Pilot Partograph study 2
Prof Sue Kildea0 sites246 target enrollmentMay 8, 2015
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- ormal Labour
- Sponsor
- Prof Sue Kildea
- Enrollment
- 246
- Status
- Terminated
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Nulliparous women in spontaneous labour who are:
- •\* At term (between 37 and 41 weeks plus 6 days gestation) with a singleton pregnancy, a cephalic (head down) presentation and cervical
- •dilatation of 4cm or greater
- •\* Equal to or greater than 18 years of age and able to provide informed
- •\* Defined as ‘low risk’ i.e. no history of: stillbirth or neonatal death, three or more consecutive miscarriages, previous fetal death in utero, previous
- •preterm birth (less than 32 weeks), previous mid\-trimester loss/cervical incompetence/cone biopsy/known uterine anomaly, previous early onset of pre\-eclampsia (less than 32 weeks gestation), or rhesus isoimmunisation;
- •no complications during the current pregnancy (such as
- •multiple pregnancy or fetal abnormality); and no precluding medical conditions (such as cardiac disease, essential hypertension, renal disease,
- •pre\-existing diabetes, previous gestational diabetes, epilepsy, severe asthma, substance use, significant psychiatric disorders, age greater than
- •40 years, body mass indexless than 17 or greater than 35\).
Exclusion Criteria
- •Private insurance status (this refers to women who utilise their health insurance to access maternity care from an obstetrician of their choice)
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
A pilot randomised controlled trial to determine the effect of a physiological (step) versus a standard action (slope) labour progress lines on the rate of spontaneous vaginal birth amongst low risk women in labour for the first timeACTRN12614000786695Prof Sue Kildea100
Not yet recruiting
Not Applicable
Measuring the clinical effectiveness and healthcare experiences for women undergoing a balloon induction of labour, where the balloon is used for 6 hours compared to 12 hours.Induction of labourReproductive Health and Childbirth - Childbirth and postnatal careACTRN12618000510246Mater Misericordiae Ltd858
Terminated
Not Applicable
Capacity for informed consent during labourInformed consent during labourReproductive Health and Childbirth - Childbirth and postnatal careReproductive Health and Childbirth - Normal pregnancyACTRN12614000456651Royal Hospital for Women49
Completed
Not Applicable
A randomised, controlled trial of a single versus a four intradermal sterile water injection technique for relief of continuous lower back pain during labour.Women experiencing significant back pain in labourReproductive Health and Childbirth - Childbirth and postnatal careACTRN12609000964213Mater Mothers' Hospital320
Terminated
Not Applicable
Impact on Caesarean Rates following Injections of Sterile Water (ICARIS) – A randomised controlled trial.abour and birthLabour and birthReproductive Health and Childbirth - Childbirth and postnatal careACTRN12611000221954Mater Health Services1,866