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Clinical Trial Summary

To evaluate the duration of labour (active phase of labour) in nulliparous women with gestations between 37 and 41 6/7 weeks when 20 mg of Hyoscine butylbromide was applied intravenously and compared with similar patients that received a placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03441217
Study type Interventional
Source Saint Thomas Hospital, Panama
Contact
Status Completed
Phase N/A
Start date July 12, 2019
Completion date November 30, 2019

See also
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