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Your journey
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3Review
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More info
You can access this
clinical trial
if you have
Contraception, Postpartum Depression or Lactation
and you are
over 18
years old
4
The primary goal of this phase is to monitor the long-term effects.
The treatment is already on the market.
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The purpose

The investigators plan to enroll 184 women who are planning to breastfeed and use DMPA after delivery to find out whether the timing of postpartum administration of DMPA (prior to hospital discharge or 4-6 weeks after delivery) affects the duration or exclusivity of breastfeeding among women who plan to breastfeed their infants.

Provided treatments

  • Drug: Depot medroxyprogesterone acetate
  • Drug: Depot medroxyprogesterone acetate

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01463202. The sponsor of the trial is Beatrice Chen and it is looking for 184 volunteers for the current phase.
Official trial title:
Effect of Timing of Postpartum Depot Medroxyprogesterone Acetate Administration on Breastfeeding Continuation, Contraceptive Continuation, and Postpartum Depression: a Randomized Trial