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Clinical Trials/CTRI/2011/08/001933
CTRI/2011/08/001933Recruiting未知

IMMEDIATE POSTPARTUM INTRAUTERINE CONTRACEPTIVE DEVICE INSERTIO

I0 sites30 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor
Enrollment
30
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •females of reproductive age were selected in immediate postpartum period Incidence(i.e. immediately following delivery of placenta, intracaesarean or within 48 hours after delivery of baby)

Exclusion Criteria

  • •prolonged rupture of membrane18 hr
  • •unresolved postpartum haemorrhage
  • •distorted uterus
  • •extensive genital trauma
  • •trophoblastic disease

Investigators

Sponsor
I

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