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Clinical Trials/ACTRN12620001000998
ACTRN12620001000998
Recruiting
未知

A feasibility study to determine the ability of an intra-uterine device (IUD) insertion device to accurately place an IUD in acute postpartum women.

Michael Stitely0 sites10 target enrollmentOctober 6, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Intrauterine Contraception
Sponsor
Michael Stitely
Enrollment
10
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 6, 2020
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Michael Stitely

Eligibility Criteria

Inclusion Criteria

  • 1\. Age 18 or older.
  • 2\. Immediately post vaginal delivery, within 10 minutes of placental delivery.
  • 3\. Previously expressed desire for PPIUD and has signed study consent documents.

Exclusion Criteria

  • 1\. Active uterine infection and no fever in labour.
  • 2\. Having active sexually transmitted infection or other lower genital tract infection.
  • 3\. Known to have ruptured membranes for more than 24 hours prior to delivery.
  • 4\. Known uterine abnormalities e.g., Bicornuate/septate Uterus, uterine myomas,
  • 5\. Manual removal of the placenta.
  • 6\. Unresolved postpartum haemorrhage or postpartum uterine atony requiring use of additional oxytocic agents in addition to Active Management of the third stage of labour.

Outcomes

Primary Outcomes

Not specified

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