38 studies found for:    Open Studies | "Intrauterine Devices"
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Rank Status Study
1 Recruiting Pain Control for Intrauterine Device Placement: A Trial of Ketorolac Prior to Intrauterine Device Placement
Condition: Pain Control With IUD Insertion
Interventions: Drug: Ketorolac;   Drug: Normal Saline
2 Recruiting Comparison of the Levonorgestrel IUD and the Copper IUD Placed in the Immediate Postplacental Period: A Randomized Controlled Trial
Condition: Postplacental IUD Placement
Interventions: Device: Mirena (LNG-IUS);   Device: Paragard (Copper IUD)
3 Unknown  Study About Patients Using Copper Intrauterine Device
Condition: Copper Intrauterine Device Induced Bleeding
Intervention:
4 Not yet recruiting Study of Local Anesthesia as a Method to Decrease IUD Insertion Related Pain
Conditions: IUD Insertion Complication;   Pain Control
Intervention: Drug: Lidocaine
5 Recruiting Sub Lingual Misoprostol Before IUD Insertion in Women With Only Previous Cesarean Section
Condition: IUD Insertion
Interventions: Drug: Misoprostol;   Drug: Placebo
6 Recruiting Early Postpartum Intrauterine Device (IUD) Placement
Condition: Contraception
Intervention: Drug: Levonorgestrel IUS
7 Recruiting Study of the Copper IUD or Oral Levonorgestrel and the Levonorgestrel IUD for Women Seeking Emergency Contraception
Condition: Emergency Contraception
Interventions: Drug: Copper IUD;   Drug: Levonorgestrel IUD
8 Recruiting Levonorgestrel Intrauterine Device (IUD) to Treat Complex Atypical Hyperplasia (CAH) and Grade 1 Endometrioid Endometrial Carcinoma (G1EEC)
Conditions: Hyperplasia;   Endometrial Cancer
Intervention: Device: Levonorgestrel IUD
9 Unknown  The Effect of a Levonorgestrel-releasing Intrauterine Device (IUD) Versus a Copper Containing IUD on Risk of Blood Clots
Condition: Blood Coagulation Disorders
Interventions: Device: Levonorgestrel-containing IUD (Mirena®);   Device: Copper-containing IUD (Paraguard®)
10 Recruiting Multivariate Assessment of the IUB Intrauterine Device Compared With a T380A IUD
Condition: Prevention of Pregnancy
Interventions: Device: SCu300A IUB intrauterine device;   Device: T380A IUD
11 Recruiting Monitoring With Ultrasound Imaging of Intrauterine Device (IUD) Position Placed Immediately After Giving Birth
Conditions: Contraception;   Postpartum
Intervention: Other: Immediate postpartum placement of IUD
12 Recruiting The Effect of Nitroglycerin on the Intrauterine Device (IUD) Insertion Experience in Nulliparous Women
Conditions: Contraception;   Pain
Interventions: Drug: Insertion of nitroglycerin ointment;   Drug: Insertion of placebo ointment
13 Unknown  Misoprostol Prior to Intrauterine Device (IUD) Insertion in Nulliparous Women
Condition: Pain
Intervention: Drug: Misoprostol
14 Not yet recruiting RAPID EC - Rct Assessing Pregnancy With Intrauterine Devices for EC
Condition: Contraception
Interventions: Drug: Copper IUD;   Drug: Levonorgestrel IUD
15 Unknown  Topical Lidocaine for Pain Control With Intrauterine Device (IUD) Insertion
Condition: Pain
Interventions: Drug: Lidocaine;   Drug: Placebo
16 Recruiting Bleeding Pattern Difference Between Levonorgestrel Intrauterine System (LNG-IUS) and Copper Intrauterine Devices (IUDs) Immediately Inserted After Abortion
Condition: Contraception
Interventions: Drug: Levonorgestrel IUS (Mirena, BAY86-5028);   Device: Copper-IUD
17 Recruiting BLIS - Breastfeeding Levonorgestrel IUD Study
Condition: Contraception
Intervention: Drug: Levonorgestrel IUD
18 Recruiting Immediate Versus Later Insertion of IUD After Medical Termination of Pregnancy
Condition: Contraception After Medical Abortion
Intervention: Procedure: Immediate IUD insertion
19 Unknown  Topical Lidocaine on the Cervix and Intra-Cervical Prior to Insertion of Intrauterine Devices
Condition: Contraception
Interventions: Drug: Lidocaine;   Drug: Lubricant
20 Not yet recruiting LNG-IUS Randomized Controlled Trial at 2-3 Weeks Postpartum
Conditions: Contraception;   Malposition of Intrauterine Contraceptive Device
Intervention: Drug: Levonorgestrel Intrauterine System (LNG-IUS)

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Indicates status has not been verified in more than two years