Menu
Menu
Menu
Menu
Background: Assisted vaginal birth is a vital health intervention that can result in better outcomes for mothers and their babies when complications arise in the second stage of labour. Unfortunately, instruments for assisted vaginal birth (forceps and ventouse) are often not utilised in settings where there is most clinical need, resulting in maternal and neonatal morbidity and mortality which could have been prevented. The BD Odon Device is a new device for assisted vaginal birth that may be able to address this unmet need. However, before dissemination, the device requires evaluation in robust clinical trials. A feasibility study to investigate the clinical impact, safety, and acceptability of the BD Odon Device for assisted vaginal birth is therefore planned. This will provide further information on acceptability, recruitment, and the outcome data required to design a future randomised controlled trial of the BD Odon Device versus Kiwi ventouse. Methods: Forty women who require an assisted vaginal birth for a recognised clinical indication will have the birth assisted with the BD Odon Device. The primary outcome is successful vaginal birth completed with the BD Odon Device. Secondary clinical outcomes include maternal and neonatal outcomes, and maternal and practitioner satisfaction. Safety data will be reviewed following every birth. Discussion: A future randomised controlled trial of the BD Odon Device versus the current standard instrument (the Kiwi ventouse) is planned. The findings of the ASSIST Study will inform the randomised controlled trial design. Trial registration: ISRCTN, ISRCTN10203171. Prospectively registered on 27 July 2018.
This feasibility study will investigate the clinical impact, safety, and acceptability of the BD Odon Device and assess the feasibility of recruiting women and data collection. It will provide vital information on acceptability, recruitment, and the outcome data required to design a future RCT of the BD Odon Device versus the Kiwi ventouse. The ASSIST Study (Assisted Vaginal Birth Study) is a non-randomised feasibility study of 40 women who require an assisted vaginal birth for a recognised clinical indication and who will all have their birth assisted with the BD Odon Device. A CONSORT diagram of the feasibility study is shown in Fig. 3. CONSORT diagram of the ASSIST feasibility study. AVB assisted vaginal birth, NIP Neonatal Infant Pain The ASSIST feasibility study will utilise only one of the devices intended for use in the eventual randomised controlled study (BD Odon Device). This is to establish the safety, acceptability, and efficacy of the BD Odon Device prior to moving to a full RCT. The intended comparator (the Kiwi ventouse) will not be evaluated in this study since published evidence on its acceptability and success rate at the intended primary site already exists [13]. Participants will be pregnant women aiming for a vaginal birth who plan to give birth at North Bristol NHS Trust (NBT), Bristol, UK. Recruitment is projected to continue for 8 months (due to the AVB rate within the department) after which time it is estimated that 40 sets of primary outcome data will have been recorded. Prospective participants will receive information on the study in early pregnancy (12 to 28 weeks) via the NBT Maternity ‘App’ (this ‘App’ is provided to all pregnant women at NBT and provides information on all aspects of their maternity care) and paper information leaflets given to women at any hospital admission. Members of the study team will then approach women after 28 completed weeks of pregnancy during antenatal appointments or antenatal admissions to discuss the study and offer women the opportunity to watch a video explaining the study. Women who are willing to take part (should they require an AVB) will then be invited to provide informed written consent. Figure 4 demonstrates the schedule of enrolment, interventions, and assessments. Schedule of enrolment, interventions, and assessments. AVB assisted vaginal birth, PN post-natal When a woman who has previously consented to participate in the study arrives on the labour ward, her eligibility to participate in the study will be re-checked by a midwife and obstetrician that have been trained in Good Clinical Practice (GCP), and verbal re-confirmation of her consent to take part in the study will be sought by a GCP-trained midwife or obstetrician. Case report forms can be found in Additional file 1. Women will be able to participate in the ASSIST Study if all of the following apply at initial consent: the woman is ≥18 years of age; the woman has a singleton pregnancy of at least 36 weeks gestation; there is a negative antenatal screen for HIV and hepatitis B; the woman is in labour and requires an assisted vaginal birth for a clinical indication (as per the Royal College of Obstetrics and Gynaecology (RCOG) Greentop Guideline 26 [8]); the RCOG specific requirements for AVB are fulfilled; the woman has effective analgesia in place during the use of the instrument (i.e. epidural, spinal or pudendal block, or perineal infiltration with local anaesthetic); and there is no obstetric indication for an alternative method of AVB. Women will not be able to take part in the ASSIST Study if: there is a diagnosis of a fetal skull abnormality precluding AVB (i.e. macrocephaly); there is a known osteogenesis imperfecta affected pregnancy; there is suspicion of a fetal bleeding disorder (von Willebrand’s disease, autoimmune thrombocytopenia (AITP), haemophilia); there is an intrauterine fetal death in the current pregnancy; the woman is sensitive to latex; the woman is currently serving a prison sentence; or the indication for AVB is a fetal bradycardia which is present, ongoing, and has not recovered. If the obstetrician attending an eligible woman during the second stage of labour, and who has previously provided informed written consent to take part in the study, determines that an AVB is indicated, they will explain this to the woman as per standard practice. If the woman agrees to an AVB, an accoucheur who has had specific training in using the BD Odon Device (Additional file 2) will assist the birth with the BD Odon Device. Should the birth not be achieved with the BD Odon Device, the accoucheur will use their clinical judgement on an individual case basis to complete the birth using ventouse, forceps, or caesarean section as appropriate. Primary, secondary, safety, and qualitative research data will be gathered regarding the assisted birth and use of the device. The primary outcome will be the proportion of births successfully assisted with the BD Odon Device. A birth will be defined as ‘successful’ if all of the six criteria in Table 1 are met. Primary outcome AVB assisted vaginal birth The maternal safety outcomes are: The neonatal safety outcomes are: The device safety outcomes are: The clinical secondary outcomes are: The women-reported secondary outcomes are: The practitioner-reported secondary outcomes are: A comprehensive assessment of the safety of the BD Odon Device will be undertaken following every attempted birth within the ASSIST Study. Outcome measures and data collected will ensure capture of any potential adverse events associated with the BD Odon Device at the time of birth by the operator and/or a member of the research team (see Additional file 1 for details of case report forms). Follow-up will be performed by the research team. In the immediate post-partum period, a member of the research team will follow-up the participant on a daily basis until discharge, collecting the day 1 data. To ensure that any serious adverse events that occur in the post-natal period are captured, an Adverse Event Reporting System will be initiated on the post-natal wards for ward staff to highlight any serious adverse events that occur after discharge from the labour ward. Post-natal staff will be asked to notify a member of the research team if any such events occur. In addition, device failure (or failure of any component) will be reported as an individual outcome measure. Follow-ups at day 7, 28, and 90 will be conducted by a member of the research team by telephoning the woman using their contact details provided to the study team. The Trial Management Group (TMG) and Sponsor will regularly review data from all births according to the schedule in Additional file 3 to ensure early identification of any trends of adverse events. All adverse events will be classified and reported according to the schedule of the Medicines and Healthcare Regulation Agency (MHRA) and the Research Ethics Committee. To facilitate the development of the main trial, information will be collected on the number of women screened, those identified as eligible and approached, and those who consented to participate both in advance of labour and again during labour where applicable. Information on data completion, i.e. questionnaire completion, completion of main outcomes, and missing data, will also be reported. Reasons for ineligibility, participation refusal, loss to follow-up, or missing data will also be explored. Women and their partners have been involved throughout the development of the ASSIST Study. Formal patient and public involvement (PPI) panels have reviewed the proposed study design, patient-facing documentation (leaflets, videos, and consent forms), and have supported both the general and specific aims of the study. The Trial Steering Committee (TSC) of the ASSIST Study includes a lay patient representative. A complete sample size of 40 women will enable the estimation of the rate of successful assisted vaginal birth of 80% to within a 95% confidence interval of ±12%. The sample size will also demonstrate AVB requiring use of a secondary instrument of 50% to within a 95% confidence interval of ±15%. The primary, secondary, and safety data will be reported as the frequency and proportion, mean (and standard deviation), or median (and interquartile range) depending on their nature and distribution. The overall rate of successful AVB birth will be reported and the frequency of unsuccessful births will be reported by the six criteria defined for success. Appropriate outcomes will be presented and broken down into subgroups by operator experience (>10 years or <10 years), indication for assisted vaginal birth (fetal compromise or other indication of AVB), participant analgesia (regional anaesthetic or other analgesia), fetal station (0 and +1 cm to spines or +2 and +3 cm to spines), and fetal position (OA or OT or OP). The overall number of safety events will be reported, as well as the number of events by the main reason for adverse events. Events related to device failure and/or mis-use of the device will also be described. The recruitment and process outcomes will be reported as frequencies and percentages. Completion rates of the clinical outcomes will also be reported. Reasons for ineligibility, refusal, loss to follow-up, or missing data will be categorised and described as frequencies. Data on numbers screened, those identified as eligible and approached, those consenting to participate both in advance of labour and again during labour where applicable, those included in follow-up and those providing questionnaire and outcome data and successful birth rates will all inform the sample size calculation of the main trial. During the trial, there will be a continuous review of mother and baby safety from the Sponsor and TMG, and a decision will be made as to whether to continue, revise, or stop the trial. Women and their babies will be followed up at 1 day, 7 days, 28 days, and 90 days following the birth. A woman and her baby will be deemed to complete their participation in the study at 90 days after the birth. Alongside the primary clinical study, an integrated qualitative study (IQS) within the feasibility study will be undertaken. This will investigate: the practitioners’ use of the device to ensure that an appropriate training package is developed for the trial; enable the intervention to be described and refined to optimise its use; and to investigate the woman’s, obstetrician’s, midwife’s, and neonatologist’s perspective of the birth and what they consider to be characteristics of a ‘good birth’. This will enable the research team to incorporate these findings into any subsequent RCT, as well as iteratively altering the ASSIST Study plan if required. The qualitative study will combine observational and interview data collection and analysis. AVBs involving successful or attempted use of the BD Odon device will be observed wherever possible. Successful or attempted births will be followed up with interviews with obstetricians, midwives, and women to triangulate their experiences and views with what has been observed. A TMG consisting of all investigators and co-investigators will be responsible for the day-to-day running of the study. The study will be overseen by two committees, the Independent Data Monitoring Committee (IDMC) and the Trial Steering Committee (TSC). The IDMC will sit after 20 and 40 births have been completed and will have no direct involvement in the running of the trial. Following both reviews, the IDMC will generate a report on the performance of the device and the safety of participants. These reports will be reviewed by the TSC and the Sponsor. The TSC will consist of an independent clinical expert, statistician, and a lay representative, together with the investigators and representative. The TSC will review all reports produced by the IDMC and make a recommendation to the Sponsor following every review to continue, modify, or halt the study. The TSC will provide oversight of the progress of the study and ensure the study is conducted according to the principles of GCP. Auditing will take place when requested by the Sponsor. Study results will be published within 1 year of completion of data collection in an appropriate peer-reviewed, open-access journal. The results will be presented at local, national, and international meetings. Summaries will also be distributed using existing parent networks. A summary of results will also be sent to all women who participated in the study, unless they express their wish not to receive such information. Results will be communicated to a lay audience by social media activities of North Bristol NHS Trust, the University of Bristol, and the research team.
