drugset / Trial / NCT01271855

Assessing Maternal Post-partum Pain With Suppositories

NCT01271855

Phase 4 Completed 100 enrolled Loyola University
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This trial will evaluate whether the routine use of belladonna/opium (B\&O) suppositories improve patients' self-reported pain control in the first 24-hours after delivery.

Timeline

Start
2009-07-22
Primary completion
2011-09-29
Completion
2011-09-29

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Belladonna Unknown 16.2 mg Rectal
Subject opium Traditional medicine (herbal / TCM) 30 mg Rectal

Indications

No indication recorded.