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Intrauterine Device Clinical Trials

A listing of Intrauterine Device medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (17) clinical trials

Comparing the Efficacy of Intrauterine Balloon and Intrauterine Contraceptive Device for the Therapy of Uterine Adhesion

Intrauterine balloon and IUD are both effective in the therapy for intrauterine adhesion. The IUD is usually inserted into the uterine after a hysteroscopic adhesiolysis and removed after two or three month later. Several investigators demonstrated its favorable effect in the recurrence of adhesion after the treatment of intrauterine adhesion. ...

Phase N/A

Early Versus Late Interval Postpartum Copper Intrauterine Device Insertion

The optimal interval between pregnancies is debated, but a duration greater than 11-18 months has been suggested as reducing complications in the subsequent pregnancy. Improved birth spacing can be a key benefit use of long-acting reversible contraception, but delay to initiation can still be problematic.So women who have recently given ...

Phase N/A

Discontinuation Rate Among Copper IUD Users

The aim of the study is to compare between primary health care unit and university family planning clinic in discontinuation rate among copper IUD users. The Research Hypothesis: (Null hypothesis) In women using copper IUD, discontinuation rate in primary health care unit and university clinic may be similar. The Research ...

Phase N/A

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).

The intrauterine device (IUD) is a long-term birth control method that has demonstrated high contraceptive efficacy and effectiveness due to its high compliance, adherence and persistence of use. The IUD has a global prevalence rate around 14% in women of reproductive age. Side effects are the main reason for IUD ...

Phase

Different Analgesics Prior to Intrauterine Device (IUD) Insertion: Is There Any Evidence?

A randomized clinical controlled trial of women undergoing IUD insertion. Participants in the study groups will be randomly assigned by labeled opaque envelopes to either1% lidocaine (Xylocaine 1%, Astra Zeneca, Egypt), misoprostol (Sigma, Egypt), naproxen (Naprosyn, Syntax, Egypt) or placebo tablets.

Phase N/A

Lidocaine In-situ Gel Before Intrauterine Device Insertion

Intrauterine device can cause pain and discomfort in several ways: Use of the tenaculum to grasp the cervix and straighten the uterus for proper insertion; trans-cervical actions including measuring uterine depth, inserting the insertion tube, and removing the tube; and placement of the device in the uterus.

Phase

Expulsion of Immediate Postplacental Copper Intrauterine Devices at Six Months: A Prospective Cohort Study

The purpose of the study is to measure the rate of expulsion of the copper intrauterine device (ParaGard) when placed immediately after childbirth. Many women in the United States have unintended pregnancies. Long-acting reversible birth control methods, like the copper intrauterine device (IUD), help prevent unintended pregnancy. This is because, ...

Phase N/A

Cold Compress for Pain Associated With Intrauterine Device Insertion

This study will be a prospective randomized controlled trial comparing cold compression to no intervention immediately prior to and during intrauterine device insertion. Inclusion criteria include all non-pregnant women, 18 years of age or older, presenting to the VCU Women's Health clinics with desired IUD placement. Subjects will be identified ...

Phase N/A

A Cross-sectional Observational Multicenter Study to Assess the Reasons for Choosing the 3-year Hormonal IUD and Level of IUDs Knowledge Among Women Aged 18 to 29 Years

A cross-sectional, observational multicenter study to assess the reasons for choosing the 3-year hormonal IUD and level of IUDs knowledge among women aged 18 to 29 years. The study will be conducted in standard clinical practice conditions at public and private gynecology clinics and during a single study visit. Approximately ...

Phase N/A

The Effect of a Levonorgestrel-releasing Intrauterine Device (IUD) Versus a Copper Containing IUD on Risk of Blood Clots

This is a randomized controlled trial to assess the effect of a levonorgesterel-releasing intrauterine device (LNG IUD, Mirena®) versus a copper IUD (Paraguard®) on coagulation parameters known to be associated with risk of thrombosis (blood clots). Both the LNG IUD and the copper IUD are FDA approved devices for contraception. ...

Phase N/A