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Intrauterine Device

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61. Impact of the levonorgestrel-releasing intrauterine device on controlled ovarian stimulation outcomes. (PubMed)

Impact of the levonorgestrel-releasing intrauterine device on controlled ovarian stimulation outcomes. To report differences in ovarian stimulation outcomes in women using a levonorgestrel-releasing intrauterine device (LNG-IUD).Retrospective cohort study.University-based infertility practice.Female patients pursuing either social oocyte cryopreservation or oocyte donation.Chart review of all female patients presenting from January 1, 2012, to June 30, 2017, for social oocyte cryopreservation

2018 Fertility and Sterility

62. Sigmoid colon translocation of an intrauterine device misdiagnosed as a colonic polyp: A case report. (PubMed)

Sigmoid colon translocation of an intrauterine device misdiagnosed as a colonic polyp: A case report. Intrauterine contraceptive devices (IUDs) are recommended as a means of contraception. Translocation of IUD is a rare and serious complication. Colonic inflammatory mass caused by translocated IUD initially misdiagnosed as a colonic polyp is extremely rare and has not been reported yet.This report presents a case of sigmoid colon translocation of intrauterine device on a 37-year-old female (...) patient. Colonoscopy was performed due to her complain of repeated blood in stools and subsequently the patient was misdiagnosed as a sigmoid colon polyp. Nonetheless, the "polyp" was not able to be removed endoscopically.Sigmoid colon translocation of an intrauterine device.To further clarify the diagnosis, computed tomography (CT) scan was performed and the "polyp" was confirmed to be caused by a translocated IUD.The translocated IUD was removed easily by surgery, and the patient recovered soon

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2018 Medicine

63. Factors associated with low-lying intrauterine devices: a cross-sectional ultrasound study in a cohort of African-American women. (PubMed)

Factors associated with low-lying intrauterine devices: a cross-sectional ultrasound study in a cohort of African-American women. The object of this study is to examine factors and symptoms associated with low-lying IUDs as defined by ultrasound.This is a cross-sectional sub-study of participants in the Study of Environment, Life-style, and Fibroids (SELF). SELF participants had screening ultrasounds for fibroids at study enrollment; those with an IUD in place are included in this sub-study

2018 Contraception

64. Colonoscopic Removal of an Intrauterine Device That Had Perforated the Rectosigmoid Colon (PubMed)

Colonoscopic Removal of an Intrauterine Device That Had Perforated the Rectosigmoid Colon The intrauterine device (IUD) is a widely used contraceptive method. One of the most serious and rare complications of using an IUD is colon perforation. We report a case of colonoscopic removal of an IUD that had perforated into the rectosigmoid colon in a 42-year-old woman who presented with no symptoms. Colonoscopy showed that the IUD had penetrated into rectosigmoid colon wall and that an arm

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2018 Annals of coloproctology

65. Postpartum intrauterine device placement: a patient-friendly option (PubMed)

Postpartum intrauterine device placement: a patient-friendly option Women in the United States are increasingly choosing an intrauterine device (IUD) for contraception. Since the postpartum period is an important time to consider a patient's need for contraception, offering postpartum IUD placement is considered best practice. Effective implementation of postpartum IUD placement occurs within a context of shared decision making wherein patients are given full information about all options

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2018 Contraception and Reproductive Medicine

66. Dimensional analysis of the endometrial cavity: how many dimensions should the ideal intrauterine device or system have? (PubMed)

Dimensional analysis of the endometrial cavity: how many dimensions should the ideal intrauterine device or system have? The geometrical shape of the human uterus most closely approximates that of a prolate ellipsoid. The endometrial cavity itself is more likely to also have the shape of a prolate ellipsoid especially when the extension of the cervix is omitted. Using this information and known endometrial cavity volumes and lateral and vertical dimensions, it is possible to calculate (...) and breadth measurements indicate that the AP diameter may vary from 6.29 to 38.2 mm. These measurements confirm the difficulty of getting a fixed-frame intrauterine device (IUD) to accommodate to a space of highly variable dimensions. This is especially true of three-dimension IUDs. A one-dimensional frameless IUD is most likely to be able to conform to this highly variable space and shape.The endometrial cavity may assume many varied prolate ellipsoid configurations where one or more measurements may

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2018 International journal of women's health

67. Clinical characteristic and intraoperative findings of uterine perforation patients in using of intrauterine devices (IUDs) (PubMed)

Clinical characteristic and intraoperative findings of uterine perforation patients in using of intrauterine devices (IUDs) Intrauterine devices (IUDs) are the most popular form of contraception used worldwide; however, IUD is not risk-free. IUD migrations, especially uterine perforations, were frequently occurred in patients. The aim of this study was to investigate the clinical characteristics and intraoperative findings in patients with migrated IUDs.29 cases of uterine perforation (...) groups. Majority of contraceptive intrauterine devices was the copper-releasing IUDs. Furthermore, patients who used V-shaped IUD showed significantly higher incidence of pelvic adhesions when compared with the users of O-shaped IUDs.Unique clinical characteristics of IUD migration were identified in patients with uterine perforation. Hysteroscopy and/or laparoscopy were the effective approaches to remove the migrated IUDs. Improving operating skills is required at the lower level of health care

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2018 Gynecological surgery

68. Calcified retained intrauterine device in the setting of a vesicovaginal fistula (PubMed)

Calcified retained intrauterine device in the setting of a vesicovaginal fistula 29552499 2019 02 26 2214-4420 17 2018 Mar Urology case reports Urol Case Rep Calcified retained intrauterine device in the setting of a vesicovaginal fistula. 106-108 10.1016/j.eucr.2018.01.023 Scambia Jillian R JR Division of Urology, John H. Stroger, Jr. Hospital of Cook County, Chicago, IL, USA. Lombardo Lindsay L Division of Urology, John H. Stroger, Jr. Hospital of Cook County, Chicago, IL, USA. Division (...) Reports 2018 01 31 United States Urol Case Rep 101626357 2214-4420 Intrauterine device Transabdominal fistula repair Vaginal foreign bodies Vesicovaginal fistula 2018 01 10 2018 01 21 2018 3 20 6 0 2018 3 20 6 0 2018 3 20 6 1 epublish 29552499 10.1016/j.eucr.2018.01.023 S2214-4420(18)30011-1 PMC5850877 Obstet Gynecol. 2010 Nov;116(5):1079-87 20966692 Int J Radiat Oncol Biol Phys. 2014 May 1;89(1):88-95 24725693 Int Urogynecol J. 2014 Dec;25(12):1699-706 25062654

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2018 Urology case reports

69. Use and discontinuation of intrauterine contraceptive device in the Greater Accra Region of Ghana (PubMed)

Use and discontinuation of intrauterine contraceptive device in the Greater Accra Region of Ghana The intrauterine contraceptive device is one of the modern long-acting and reversible contraception that is very safe and effective. Yet, less than 2 % of women are using intrauterine devices in Ghana. This study therefore explored the experiences and barriers to intrauterine contraceptive device use and discontinuation in Greater Accra Region, Ghana.Intrauterine contraceptive device users (...) was created and a series of categories for the main themes that emerged from the transcripts were developed. The transcribed data was organized, coded and manually thematically analysed in word. Study results were presented in tables and quotes from respondents.Results showed that key motivations for intrauterine contraceptive device use include effectiveness, benefits, and efficacy of the device, fertility regulation, peace of mind, contraceptive method switching, health provider effects, desire for long

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2018 Contraception and Reproductive Medicine

70. Hydronephrosis due to a Migrated Intrauterine Device into the Ureter: A Very Rare Case (PubMed)

Hydronephrosis due to a Migrated Intrauterine Device into the Ureter: A Very Rare Case Intrauterine device (IUD) insertion is a long-acting and one of the most effective modes of reversible contraception. Complications that most commonly arise following IUD insertion are failed insertion, pain, vasovagal reactions, infection, menstrual abnormalities, and expulsion. In this paper, we present the case of a woman who experienced hydronephrosis due to the migration of IUD into the ureter after 30

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2018 The Eurasian journal of medicine

71. Hysteroscopic-guided Removal of Retained Intrauterine Device: Experience at an Academic Tertiary Hospital (PubMed)

Hysteroscopic-guided Removal of Retained Intrauterine Device: Experience at an Academic Tertiary Hospital Removal of an intrauterine device can be easily done when the string is visible during speculum exam. The task becomes challenging when the string is no longer visible.The in-patient and out-patient medical records of all patients admitted for hysteroscopic-guided intrauterine device removal from January 2013 to December 2015 from a tertiary academic government hospital were retrieved

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2018 Gynecology and Minimally Invasive Therapy

72. Misoprostol for Cervical Ripening Before Copper Intrauterine Device Removal

Misoprostol for Cervical Ripening Before Copper Intrauterine Device Removal Misoprostol for Cervical Ripening Before Copper Intrauterine Device Removal - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more (...) . Misoprostol for Cervical Ripening Before Copper Intrauterine Device Removal The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03600064 Recruitment Status : Recruiting First Posted : July 25, 2018 Last Update Posted : July 25

2018 Clinical Trials

73. Comparison of Pain Level During Intrauterine Device (IUD) Insertion Between Conventional and Direct Method

Comparison of Pain Level During Intrauterine Device (IUD) Insertion Between Conventional and Direct Method Comparison of Pain Level During Intrauterine Device (IUD) Insertion Between Conventional and Direct Method - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) ). Please remove one or more studies before adding more. Comparison of Pain Level During Intrauterine Device (IUD) Insertion Between Conventional and Direct Method (KIDDS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier

2018 Clinical Trials

74. Surveillance Study of the Contraceptive Intrauterine Device UT380®

Surveillance Study of the Contraceptive Intrauterine Device UT380® Surveillance Study of the Contraceptive Intrauterine Device UT380® - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Surveillance Study (...) of the Contraceptive Intrauterine Device UT380® (CCDDIUUT) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03642171 Recruitment Status : Recruiting First Posted : August 22, 2018 Last Update Posted : September 3, 2018 See Sponsor

2018 Clinical Trials

75. Immediate Postpartum Insertion of Contraceptive Intrauterine Devices

Immediate Postpartum Insertion of Contraceptive Intrauterine Devices Immediate Postpartum Insertion of Contraceptive Intrauterine Devices - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Immediate Postpartum (...) Insertion of Contraceptive Intrauterine Devices The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03657602 Recruitment Status : Not yet recruiting First Posted : September 5, 2018 Last Update Posted : January 25, 2019 See

2018 Clinical Trials

76. Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women.

Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women. Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women. - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) ). Please remove one or more studies before adding more. Vaginal Dinoprostone Administration Prior to a T380A Intrauterine Device Insertion in Nulliparous Women. The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03686085

2018 Clinical Trials

77. Study on Medical Records of Women Using a Coil (Intrauterine Device = IUD) for Birth Control to Analyze the Risk That a Coil Will Slip Out or Perforate the Womb in Relation to Breastfeeding, to the Point in Time When the Coil Was Inserted After Childbirth

Study on Medical Records of Women Using a Coil (Intrauterine Device = IUD) for Birth Control to Analyze the Risk That a Coil Will Slip Out or Perforate the Womb in Relation to Breastfeeding, to the Point in Time When the Coil Was Inserted After Childbirth Study on Medical Records of Women Using a Coil (Intrauterine Device = IUD) for Birth Control to Analyze the Risk That a Coil Will Slip Out or Perforate the Womb in Relation to Breastfeeding, to the Point in Time When the Coil Was Inserted (...) After Childbirth and in Relation to Different Types of Coils. - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Study on Medical Records of Women Using a Coil (Intrauterine Device = IUD) for Birth Control

2018 Clinical Trials

78. Adhesion and biofilm formation of Candida parapsilosis isolated from vaginal secretions to copper intrauterine devices (PubMed)

Adhesion and biofilm formation of Candida parapsilosis isolated from vaginal secretions to copper intrauterine devices Candida parapsilosis is one of the main species that is able to adhere to forming biofilms on inert materials. Adhesion is the first step towards the colonization and invasion of host cells during the infectious process. Among the infections, vulvovaginal candidiasis is increasingly common. The objective was to evaluate the profile of adherence and biofilm formation of eight (...) isolates of C. parapsilosis on the metal used in intrauterine devices (IUDs).Eight strains of C. parapsilosis presenting strong adhesion and biofilm formation properties were isolated from vaginal secretions in a previous study. To assay the adhesion and biofilm formation, copper fragments were made and cultivated in tubes containing 3 mL of phosphate-buffered saline and incubated for 6 and 24 h at 37 °C to evaluate biofilm formation. After incubation, the intensity of adherence and of biofilm

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2018 Revista do Instituto de Medicina Tropical de São Paulo

79. Studies of acute and subchronic systemic toxicity associated with a copper/low-density polyethylene nanocomposite intrauterine device (PubMed)

Studies of acute and subchronic systemic toxicity associated with a copper/low-density polyethylene nanocomposite intrauterine device The physiologic safety of devices and materials intended for clinical implantation should be evaluated. This study, a logical extension of our previous work, aimed to investigate the safety of a novel contraceptive device, the copper/low-density polyethylene nanocomposite intrauterine device (nano-Cu/LDPE IUD), through studies of its potential toxicity after

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2018 International journal of nanomedicine

80. Effect of Baseline Menstrual Bleeding Pattern on Copper Intrauterine Device Continuation. (PubMed)

Effect of Baseline Menstrual Bleeding Pattern on Copper Intrauterine Device Continuation. Heavy menstrual bleeding is a leading cause of copper intrauterine device discontinuation. Thus, girls and women with heavy baseline menstrual bleeding may be at increased risk for early copper intrauterine device discontinuation.Our objective was to assess if there was an association between baseline menstrual bleeding pattern prior to intrauterine device insertion and discontinuation rate at 12 months (...) among study participants who chose copper intrauterine device at baseline.We performed a secondary analysis of the Contraceptive CHOICE Project, a prospective observational cohort study of 9256 girls and women offered no-cost contraception for 2-3 years. Included in our study were participants who chose copper intrauterine device for contraception and for whom method continuation data at 12 months were available. Prior to contraception initiation, participants were asked to qualify their menstrual

2018 American Journal of Obstetrics and Gynecology

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