Lessons learnt from the multi-centre LAparoscopic Versus Abdominal hysterectomy (LAVA) randomised controlled trial
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Original Articles
VOLUME: 16 ISSUE: 1
P: 35 - 45
March 2024

Lessons learnt from the multi-centre LAparoscopic Versus Abdominal hysterectomy (LAVA) randomised controlled trial

Facts Views Vis ObGyn 2024;16(1):35-45
1. Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, B15 2TG UK and Institute of Metabolism and Systems Research, University of Birmingham, B15 2TT, UK
2. Institute of Applied Health Research, University of Birmingham, Birmingham, B15 2TT, UK
3. University Hospitals of North Midlands NHS Foundation Trust, Stoke-on-Trent, ST4 6QG
4. Institute of Applied Health Research, University of Birmingham, Birmingham, B15 2TT, UK
5. School of Health and Population Sciences, University of Birmingham, B15 2TT UK
6. Birmingham Clinical Trial Unit, University of Birmingham, Birmingham, B15 2TT, UK
7. Birmingham Women’s NHS Foundation Trust, Birmingham, B15 2TG UK
8. Birmingham Women’s and Children’s NHS Foundation Trust, Mindelsohn Way, Edgbaston, Birmingham, B15 2TG, UK
9. University College London Hospital, London NW1 2PG and University College London Elizabeth Garrett Anderson Institute for Women’s Health, London WC1E 6AU
10. Aberdeen Royal Infirmary, NHS Grampian, Aberdeen, AB25 2ZN and University of Aberdeen AB24 3FX
11. Birmingham Women’s NHS Foundation Trust, Birmingham, B15 2TG UK and University of Birmingham, B15 2TT UK
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Background: The LAparoscopic Versus Abdominal hysterectomy (LAVA) randomised controlled trial comparing laparoscopic hysterectomy (LH) and abdominal hysterectomy (AH) closed prematurely on the grounds of futility. Here we identify the challenges faced and lessons learnt.

Objectives: To explore the views and experiences of clinical/research staff in order to understand how these might act as barriers to trial participation and recruitment.

Materials and Methods: Review of the trial progress and collation of the views and experiences of clinical/ research staff on all aspects of the trial. Data were collected from transcribed conversations, email, phone, or video conferencing interactions and analysed descriptively.

Main outcome measures: Site set-up milestones, recruitment rates and reasons provided by clinical/research staff for site’s declining to participate. Opinions, preferences and experiences of clinicians/researchers and challenges to participation and recruitment.

Results: The mean time from initial site contact to opening was 253 days and 68 days to randomise their first participant. 265 patients were screened from 13 sites over 13 months, 154 were eligible, and 75 (59%) were randomised. Of the 53 not randomised, 23 (43%) women preferred LH whilst 6 (11%) preferred AH. The main reasons given for failure to recruit or activate set-up in the 21 sites open or in set-up, were lack of research/ clinical capacity imposed by the COVID-19 pandemic and lack of clinician equipoise.

Conclusions: The main reasons for the LAVA trial failure were lack of equipoise amongst surgeons and the adverse impact of the COVID-19 pandemic on clinical/research services.