Table 1

Characteristics of 152 study participants at entry to the study

CharacteristicControl group (n=73)Treatment group (n=79)p
[n or mean (% or SD) or *median (IQR)]
Age (years)28.1 (6.1)25.2 (5.0)0.002
BMI at booking-in (kg/m2)*24 (21–32)*28 (23–32)*0.06
Smoker19 (26.0)24 (36.7)0.16
Previous contraception used
 Implanon®15 (20.6)33 (41.8)0.005
 COCP49 (67.1)59 (74.7)0.31
 Condoms29 (39.7)19 (24.1)0.04
 DMPA11 (15.1)11 (13.9)0.84
 LNG-IUS0 (–)2 (2.5)0.50
 POP3 (4.1)3 (3.8)1.00
Previous unplanned pregnancy35 (49.3)50 (64.1)0.07
Parity*2 (1–3)*2 (1–3)*0.96
Gestation (days)273 (18.3)272 (21.0)0.70
Caesarean delivery27 (37.0)27 (34.2)0.72
Birth weight (g)3307.9 (657.3)3392.0 (689.9)0.44
Fully breastfeeding42 (57.5)40 (50.6)0.49
Partially breastfeeding4 (5.5)8 (10.1)
Day postpartum Implanon inserted*–*2 (0.99)*
PPH 0.72
 No (less than 500 ml)58 (79.5)60 (75.9)
 500–1000 ml11 (15.1)12 (15.2)
 >1000 ml4 (5.5)7 (8.9)
Contraception used at follow-up 
 COCP5 (6.8)
 Condoms30 (41.1)
 Nil/breastfeeding32 (43.8)
 Tubal ligation (at Caesarean delivery)6 (8.2)
  • *Data are median and IQR.

  • BMI, body mass index; COCP, combined oral contraceptive pill; DMPA, depot medroxyprogesterone acetate; IQR, interquartile range; LNG-IUS, levonorgestrel intrauterine system; POP, progestogen-only oral contraceptive pill; PPH, postpartum haemorrhage; SD, standard deviation.