# Study to Evaluate the Safety and Efficacy of Seasonale for Treatment of Low Bone Mineral Density

> **NCT00117260** · PHASE3 · WITHDRAWN · sponsor: **Duramed Research**

## Conditions studied

- Osteopenia

## Interventions

- **DRUG:** Seasonale (levonorgestrel and ethinyl estradiol)

## Key facts

- **NCT ID:** NCT00117260
- **Lead sponsor:** Duramed Research
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** 2005-07
- **Primary completion:** 2007-07
- **Final completion:** 2007-08
- **Target enrollment:** 0 (ACTUAL)
- **Why stopped:** Sponsor decision
- **Last updated:** 2013-08-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00117260

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00117260, "Study to Evaluate the Safety and Efficacy of Seasonale for Treatment of Low Bone Mineral Density". Retrieved via AI Analytics 2026-07-12 from https://api.ai-analytics.org/clinical/NCT00117260. Licensed CC0.

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