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Clinical Trial Summary

In this study the effect of piroxicam on the ovulation will be evaluated. Therefore piroxicam will be administered as a single-dose after onset of LH surge (luteinizing hormone, hormone which triggers ovulation).

Additionally blood levels of endogenous hormones (hormones produced by your body) will be measured and transvaginal ultrasound examinations will be conducted at regular intervals. In addition the concentration of piroxicam in blood will be determined in regular intervals.

With regards to the tolerability of the study drug subjects will be asked regularly how they feel.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)


Related Conditions & MeSH terms


NCT number NCT01320709
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date March 2011
Completion date May 2012

See also
  Status Clinical Trial Phase
Completed NCT01096485 - Cross-over Study to Prove Bioequivalence Between Two Oral Formulations of Levonorgestrel Phase 1
Completed NCT01096498 - Cross -Over Study to Prove Bioequivalence Between Two Oral Formulations of Levonorgestrel Phase 1