| Methods | Random assignment. | |
| Participants | 3998 patients recruited in 8 US collaborating centres. Inclusion criteria: favourable placental position allowing both procedures to be performed, gestational age between 49 and 90 days. Exclusion criteria: active genital herpes, active vaginal bleeding or cervical polyps. 1190 randomised to TC CVS and 1163 to TA CVS | |
| Interventions | TA or TC CVS. TC being performed with a plastic catheter and TA with an 18 to 22 G spinal needle | |
| Outcomes | Sampling success, pregnancy outcome. | |
| Notes | Initial cohort of 2353 women presented who delivered before July 1 1989 | |
| Risk of bias | ||
| Item | Authors’ judgement | Description |
| Allocation concealment? | Yes | A - Adequate |
AC: amniocentesis
CRL: crown rump length
CVS: chorionic villus sampling
EA: early amniocentesis
G: gauge
TA: transabdominal
TC: transcervical
vs: versus