Clinical Trials Logo

Clinical Trial Summary

This study aims to use validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD.


Clinical Trial Description

New users of the intrauterine device (IUD) are most likely to discontinue use within the first six months after insertion. The most common reason for discontinuation of the copper IUD is symptoms related to bleeding. Research looking at disturbances in bleeding patterns among new IUD users is sparse and dated. Perceived changes in vaginal bleeding may impact method satisfaction, acceptability, and continuation. There is a need for updated research evaluating changes in bleeding patterns in order for providers to better counsel patients on what to expect during the months after initiation of an IUD. A variety of methods to evaluate bleeding profiles are available. The World Health Organization (WHO) published recommendations for methods of collection and analysis of bleeding patterns. The WHO method includes data collection on bleeding days (days when blood loss requires the use of a menstrual pad or tampon) and spotting days (when no protection was needed) using 90-day referent periods. A second tool, the pictorial blood loss assessment chart (PBAC) has been shown to be an inexpensive and objective method of assessing blood loss. The PBAC takes into consideration how heavy blood flow is as well as the number of sanitary napkins and tampons used. Additionally, new technologies (including mobile period tracking applications) have made retrospective collection of bleeding data more feasible and prospective data collection more accurate. This study aims to incorporate these validated tools as well as new technology to examine changes in bleeding patterns among women who are initiating the copper T380A IUD. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02311478
Study type Interventional
Source University of Utah
Contact
Status Completed
Phase N/A
Start date December 2014
Completion date February 2017

See also
  Status Clinical Trial Phase
Completed NCT03708692 - Menstrual Cycle Phases on Recovery and Cognitive Function
Not yet recruiting NCT05936424 - Menstrual Cycle Phase Based Training N/A
Recruiting NCT05683119 - The Effect of Menstrual Cycle and Oral Contraceptive Pill Phase on Aspects of Exercise Physiology N/A
Completed NCT03708679 - Effects of Menstrual Cycle on Preoperative Anxiety
Recruiting NCT05802277 - Characterization of the Mechanical Properties of the Hamstring Muscle Group in Female. N/A
Recruiting NCT03299179 - The Effects of the Female Hormones on Cerebral Perfusion
Not yet recruiting NCT05088122 - Hormonal Effect of Different Menstrual Phases on Dynamic Balance in Postpubertal Females
Recruiting NCT06072391 - Investigating the Endocrine-metabolic-immunological Axis During the Female Menstrual Cycle by Functional Genomics
Completed NCT06086262 - Hand Grip Strength in Athletic and Non-Athletic Girls at Different Phases of Menstrual Cycle
Recruiting NCT04196595 - Apple Women's Health Study
Recruiting NCT06214442 - Effects of the Menstrual Cycle on Triceps Surae Properties in Women
Active, not recruiting NCT05347667 - Menstrual Cycle Phase Muscle Protein Synthesis N/A
Completed NCT04286828 - Position Sense, Balance, and Dual Task Performance at the Menstrual Cycle in Females With Multiple Sclerosis
Completed NCT05576740 - Influence of Menstrual Cycle Stages on Female Athletes
Completed NCT00456222 - Impact of Sleep Disruption on the Menstrual Cycle N/A
Completed NCT00128726 - The Effects of Continuous Administration of a Monophasic Oral Contraceptive on Bleeding Days and Endometrial and Ovarian Function Phase 1
Not yet recruiting NCT06060574 - Menstrual Cycle and Platelet-rich Fibrin
Recruiting NCT06142097 - Sensor Technology Assessments of Reproductive Target Study
Terminated NCT04024826 - Effects of Resistance Training on Substrate Metabolism During the Menstrual Cycle N/A
Recruiting NCT06275048 - The Influence of Oral Contraceptives During Disuse N/A