Skip to main content
. 2015 Jun 26;2015(6):CD003036. doi: 10.1002/14651858.CD003036.pub3

1. Intervention and quality summary.

Study Delivery type IUC Inadequate
 randomization
 and allocation concealment No blinding Loss to follow‐up
 > 20% Quality of evidencea
Immediate versus early insertion (10 minutes to 48 hours)
Dahlke 2011 Vaginal LNG‐IUS _ ‐1 _ Moderate
Ahuja 2014b Vaginal CuT 380A _ ‐1 Unclear Moderate
Singh 2014b Vaginal or cesarean CuT 380A ‐1 Unclear Unclear Low
Immediate versus standard insertion (weeks)
Chen 2010 Vaginal LNG‐IUS (6 to 8 weeks) _ _ _ High
Dahlke 2011 Vaginal LNG‐IUS (> 6 weeks) _ ‐1 _ Moderate
Whitaker 2014 Cesarean LNG‐IUS (4 to 8 weeks) _ _ ‐1 Moderate
Lester 2015 Cesarean CuT 380A (6 weeks) _ ‐1 _ Moderate
Ogburn 2013b Vaginal or cesarean CuT 380A (4 to 12 weeks) ‐1 Unclear Unclear Low
Immediate insertion: IUC types, modifications, or insertion techniques
Thiery 1980 Unclear Multiload 250 versus CuT 200 ‐1 Unclear _ Moderate
WHO 1980 Vaginal Copper 7 versus Lippes Loop D vs Nova‐T‐PP _ ‐1 _ Moderate
Van Kets 1987 Unclear Nova‐T‐PP vs Nova T ‐1 Unclear _ Moderate
Lavin 1983 Unclear Progestasert vs CuT 200 _ Unclear ‐1 Moderate
Apelo 1985 Vaginal IPCS‐52 vs CuT 200 _ Unclear ‐1 Moderate
Cole 1984 Vaginal
  • Delta T vs TCu 220

  • Delta Loop vs Lippes Loop D

  • Delta T (hand vs mechanical insertion)


_
Unclear ‐1 Moderate  
Kisnisci 1985 Unclear Delta Loop vs Delta T _ Unclear _ Moderate
Xu 1996 Vaginal CuT 380A: hand vs ring‐forceps insertion _ _ _ High

aRCTs considered high quality initially, then downgraded for (1) no information on randomization sequence generation or allocation concealment, or one was clearly inadequate; (2) no blinding; (3) losses > 20%; (4) information missing for both blinding and losses. Follow‐up time not shown as all studies met criteria.
 bNo full report; sources included conference abstracts and clinical trial listings.