Skip to main content

Table 2 Feasibility outcomes by centre and for all participants

From: Prostaglandin insert dinoprostone versus trans-cervical balloon catheter for outpatient labour induction: a randomised controlled trial of feasibility (PROBIT-F)

 

SGH

Medway

All participants

Women delivering in the study period (n)

2167

1126

3292

Number of eligible participants (n, %)

168 (7.75%)

106 (9.41%)

274 (8.32%)

Number of participants approached (n, %)

156 (92.9%)

74 (69.8%)

230 (83.9%)

Participants randomised (n, %)

30 (19%)

8 (10%)

38 (16.5%)

Received allocated intervention (n, %)

23/30 (76.7%)

6/8 (75.0%)

29/38 (76.3%)

Did not receive allocated intervention (n, %)

7/30 (23.3%)

2/8 (25.0%)

8/38 (21.1%)

Withdrew from trial intervention (n)

0

1

1

Complete data available (n, %)

23 (76.6%)

5 (62.5%)

28 (73.7%)

Post-natal patient questionnaire completed (n, %)

23 (76.6%)

5 (62.5%)

28 (73.7%)

Declined post-natal patient questionnaire (n)

0

1

1

Agreed for post-natal interview (n)

14

7

21

Underwent post-natal interview (n)

14

7

21

  1. SGH St. George’s University Hospital, London, Medway Medway University Hospital, Kent