Comparison of Levonorgestrel Intrauterine System, Copper T Intrauterine Device and Oral Contraceptives on Life Quality
NCT01805817 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL
Last updated 2020-08-13
Summary
Oral combined contraceptives(OC) have both progesterone and estrogen inside. Levonorgestrel-releasing intrauterine device(LNG\_IUS) has only progestagen.
Copper IUD does not have any hormonal molecule inside.
* Hypothesis is OC has more systemic beneficial or side effects than LNG\_IUS or copper IUD. LNG\_IUS has more local effects than copper IUD.
* Study reflects the beneficial or side effects of estrogen+progestagen pills and only progestogen inside device.
Conditions
- Contraceptive Methods Comparison
Interventions
- DRUG
-
YASMIN® (Drospirenone/Ethinyl Estradiol)
oral contraceptive pills
- DEVICE
-
The Copper-T is an intrauterine device (IUD)
intrauterine device for contraception
- DEVICE
-
levonorgestrel-releasing system
intrauterine device
Sponsors & Collaborators
-
Istanbul Training and Research Hospital
lead OTHER_GOV
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 50 Years
- Sex
- FEMALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2012-12-31
- Primary Completion
- 2013-12-31
Countries
- Turkey (Türkiye)
Study Locations
More Related Trials
-
Vaginal Micronized Progesterone Versus Levonorgestrel for Treatment of Non-atypical Endometrial Hyperplasia
NCT03992937 ·Status: COMPLETED ·Phase: NA
-
DIU-QoL. Quality of Life Evaluation in Intrauterine Device Users.
NCT01731132 ·Status: COMPLETED
-
Acceptability of Long-term Progestin-only Contraception in Europe
NCT00931827 ·Status: COMPLETED
-
Evaluation of the Impact of an Oral and Practical Presentation of Intrauterine Devices by a Health Professional on Women's Opinion as a Possible Contraceptive Method
NCT05317715 ·Status: UNKNOWN ·Phase: NA
-
LCS16 vs. COC User Satisfaction and Tolerability Study
NCT03074045 ·Status: COMPLETED ·Phase: PHASE3
-
LCS12 vs Combined Oral Contraceptive (COC) User Satisfaction Study
NCT01254292 ·Status: COMPLETED ·Phase: PHASE3
-
Oral Contraceptive Pills Versus Levonorgestrel-Releasing Intrauterine System for Niche-Related Abnormal Uterine Bleeding
NCT07229209 ·Status: COMPLETED ·Phase: NA
-
Effects of Hormonal Contraceptives on Liver Proteins and Coagulation Factors: A Comparison of a Contraceptive Vaginal Ring and an Oral Contraceptive
NCT00213096 ·Status: COMPLETED ·Phase: PHASE2
-
Multivariate Assessment of the IUB Intrauterine Device Compared With a T380A IUD
NCT02036177 ·Status: COMPLETED ·Phase: PHASE4
-
Menstrual Pattern Within Six Months of Levonogestrel IUS Insertion
NCT06577168 ·Status: NOT_YET_RECRUITING
-
A Study to Compare the Menstrual Bleeding Profile Among Jaydess® and Copper Intrauterine Device (IUD) Users. COLIBRI STUDY (Copper and Levonorgestrel IUD Barcelona Research Initiative).
NCT02957292 ·Status: COMPLETED ·Phase: PHASE4
-
Study Evaluating Levonorgestrel and Ethinyl Estradiol in Oral Contraception
NCT00248963 ·Status: COMPLETED ·Phase: PHASE3
-
European Active Surveillance Study of LCS12
NCT02146950 ·Status: ACTIVE_NOT_RECRUITING
-
Study to Evaluate the Pharmacokinetics of an Oral Contraceptive Containing Levonorgestrel and Ethinyl Estradiol When Co-administered With GSK1265744 in Healthy Adult Female Subjects
NCT02159131 ·Status: COMPLETED ·Phase: PHASE1
-
Quality of Life in Premenopausal Women With Heavy Menstrual Bleeding
NCT03368898 ·Status: COMPLETED
-
Stopping Heavy Periods Project
NCT02002260 ·Status: UNKNOWN ·Phase: NA
-
Discontinuation Rate Among Copper IUD Users
NCT03404102 ·Status: UNKNOWN
-
Effect of Levonorgestrel Intrauterine System on Hemoglobin Level
NCT06935968 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Assessment of the Transfer of Using Levonorgestrel Intrauterine System (LNG IUS) as a Contraceptive to Using it as Part of Hormone Replacement Therapy (HRT).
NCT00185458 ·Status: COMPLETED ·Phase: PHASE3
-
Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception
NCT01963962 ·Status: COMPLETED
-
Study Evaluating Levonorgestrel and Ethinyl Estradiol for Oral Contraception
NCT00245921 ·Status: COMPLETED ·Phase: PHASE3
-
Study of a Levonorgestrel 52 mg Intrauterine System for the Treatment of Heavy Menstrual Bleeding
NCT03642210 ·Status: COMPLETED ·Phase: PHASE3
-
A Multi-center, Open-label, Randomized, Parallel Group Study to Evaluate Pharmacokinetic Profile, Effects on the Mechanisms of Contraceptive Efficacy and Safety of Two Progestin-only Patches Containing Different Doses of Levonorgestrel (LNG)
NCT01166412 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
The Aim of This Study is to Estimate the Discontinuation Rate of Low-dose Levonorgestrel-releasing Intrauterine System Due to Self-reported Unacceptable Menstrual Bleeding Pattern in Spanish Women Who Are Using it for the First Time How Intrauterine System for Long Acting Contraception
NCT04785950 ·Status: COMPLETED
-
Comparison of the Levonorgestrel IUD and the Copper IUD Placed in the Immediate Postplacental Period: A Prospective Cohort Study
NCT02067663 ·Status: COMPLETED