# Comparison of Levonorgestrel Intrauterine System, Copper T Intrauterine Device and Oral Contraceptives on Life Quality

> **NCT01805817** · PHASE4 · WITHDRAWN · sponsor: **Istanbul Training and Research Hospital**

## Conditions studied

- Contraceptive Methods Comparison

## Interventions

- **DRUG:** YASMIN® (Drospirenone/Ethinyl Estradiol)
- **DEVICE:** The Copper-T is an intrauterine device (IUD)
- **DEVICE:** levonorgestrel-releasing system

## Key facts

- **NCT ID:** NCT01805817
- **Lead sponsor:** Istanbul Training and Research Hospital
- **Sponsor class:** OTHER_GOV
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** WITHDRAWN
- **Start date:** 2012-12
- **Primary completion:** 2013-12
- **Final completion:** —
- **Target enrollment:** 0 (ACTUAL)
- **Last updated:** 2020-08-13


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01805817

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01805817, "Comparison of Levonorgestrel Intrauterine System, Copper T Intrauterine Device and Oral Contraceptives on Life Quality". Retrieved via AI Analytics 2026-06-09 from https://api.ai-analytics.org/clinical/NCT01805817. Licensed CC0.

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