Clin2
NCT06951776Possibly a fitNot yet recruiting

Timing of teriparatide for postmenopausal osteoporosis

Circadian Rhythm DisordersOsteoporosis

Part of Bones, joints & muscles, Brain & nervous system, Hormones & metabolism clinical trials.

This trial is studying whether the time of day you receive teriparatide (a bone-building drug) affects its effectiveness for postmenopausal women with osteoporosis. You may be eligible if you have very low bone density, are between 60 and 70, and are at least 5 years past your last period.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
28 people
Ages
60 years to 70 years
Study type
Interventional

Who can take part

  • You are a woman between 60 and 70 years old.
  • You are naturally postmenopausal and it has been at least 5 years since your last period.
  • You have very low bone density, measured as a T-score of -3.0 or lower in your lower spine or hip.
  • Your vitamin D level is at least 20 ng/mL (can be corrected with supplements before testing).
  • Your blood levels of PTH and calcium are in the normal range.
  • You have not used certain medications (like bisphosphonates, teriparatide, or denosumab) within the past 6 months to 2 years, depending on the drug.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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