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Uterine Hemorrhage clinical trials

View clinical trials related to Uterine Hemorrhage.

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NCT ID: NCT02822885 Recruiting - Clinical trials for Postmenopausal Bleeding

Uterine Artery and Spiral Artery Doppler Parameters in Patients With Postmenopausal Bleeding

Start date: January 2014
Phase: N/A
Study type: Observational [Patient Registry]

This study was to investigate the diagnostic value of ultrasonography and blood flow measurements in uterine arteries and spiral arteries by transvaginal color Doppler ultrasonography in the detection of the endometrial pathology in women with postmenopausal bleeding.

NCT ID: NCT02752282 Active, not recruiting - Vaginal Bleeding Clinical Trials

Anticipatory Counseling on LNG-IUS Continuation, Utilization and Satisfaction

ACCCUSS
Start date: March 2016
Phase: N/A
Study type: Interventional

This study is a counseling intervention for new LNG-IUS users. The study explores the use of video technology to deliver anticipatory counseling on LNG-IUS side-effects, adjustment periods and bleeding changes to women newly using the LNG-IUS for contraceptive purposes. The primary aim is to understand if anticipatory counseling delivered via video can increase LNG-IUS satisfaction and continuation of the device in the first 6 months of use.

NCT ID: NCT02705222 Completed - Uterine Bleeding Clinical Trials

Comparison Between D&C and Hysteroscopy in Management of AUB in Perimenopausal Women

Start date: March 2016
Phase: N/A
Study type: Interventional

The aim of this study is to compare dilatation and curettage with hysteroscopy in obtaining an accurate diagnosis of the etiology of abnormal uterine bleeding and outlining a mode of treatment-specific to the cause.

NCT ID: NCT02614053 Active, not recruiting - Clinical trials for Antepartum Hemorrhage

Plethysmography Variability Index Monitoring for Parturients With Antepartum Hemorrhage

Start date: March 2015
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the use of continuous noninvasive intraoperative plethesmography variability index in conjunction with Hemoglobin levels monitoring using Masimo Radical-7™ Pulse CO-Oximeter during elective cesarean sections in patients with antepartum and intrapartum hemorrhage as a guide for fluid and blood transfusion practice .

NCT ID: NCT02488798 Completed - Clinical trials for Postmenopausal Bleeding

Office Hysteroscopy and 3D Power Doppler Vaginal Ultrasound in Assessment of Postmenopausal Bleeding

Start date: June 2013
Phase: N/A
Study type: Observational

100 patients with postmenopausal bleeding were assessed with 2D vaginal ultrasound and 3D power Doppler ultrasound using the international endometrial tumor analysis group and office hysteroscopy with taking samples for histopathological analysis.

NCT ID: NCT02472184 Completed - Uterine Fibroids Clinical Trials

Optimal Order of Concurrent Office Hysteroscopy and Endometrial Biopsy

Start date: October 2015
Phase: N/A
Study type: Interventional

This study will look at the optimal order in which to perform concurrent office hysteroscopy and endometrial biopsy in female patients who present for evaluation of abnormal uterine bleeding at a fibroid and endometriosis treatment center.

NCT ID: NCT02453568 Not yet recruiting - Uterine Hemorrhage Clinical Trials

Use of Tranexamic Acid for Prevention of Postpartum Hemorrhage and Routine Blood Loss in Obstetrics

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to establish that routine administration of tranexamic acid during the third stage of labor effectively reduces blood loss in vaginal deliveries.

NCT ID: NCT02385747 Completed - Vaginal Bleeding Clinical Trials

Uterine Cavity Assessment and Endometrial Hormonal Receptors in Women With Peri and Post Menopausal Bleeding

Start date: March 2015
Phase: N/A
Study type: Interventional

100 women with abnormal uterine bleeding (peri and postmenopausal) were subjected to transvaginal ultrasound , saline sonohysterography , Diagnostic hysteroscopy and fractional curettage followed by histopathological examination and immunohistochemical analysis for estrogen and progesterone receptors.

NCT ID: NCT02326922 Completed - Clinical trials for Dysfunctional Uterine Bleeding

The Use of Levonorgestrel-Releasing Device (Metraplant-E) in the Treatment of Dysfunctional Uterine Bleeding

Start date: June 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Research hypothesis: Release of levonorgestrel from Metraplant-E levonorgestrel releasing intrauterine contraceptive device is inadequate to be used as a medical line of treatment of dysfunctional uterine bleeding. The investigators aim to evaluate the therapeutic effect of the intrauterine system (Metraplant-E) in the treatment of dysfunctional uterine bleeding.

NCT ID: NCT02248194 Completed - Clinical trials for Dysfunction Uterine Bleeding

Tactile Electrosurgical Ablation in Cases of Dysfunctional Uterine Bleeding

TEA
Start date: April 2010
Phase: Phase 2
Study type: Interventional

Abnormal uterine bleeding (AUB) is any alteration in the pattern or volume of menstrual blood flow and heavy menstrual bleeding affects up to 30% of women at some time during their reproductive years. Abnormal menstruation can be due to conditions such as pregnancy complication uterine fibroids and adenomyosis, but in a large proportion of cases, the etiology is unclear, a condition generally referred to as dysfunctional uterine bleeding (DUB). Treatment options for DUB include symptomatic medical treatment or surgery, traditionally hysterectomy. Hysteroscopically guided endometrial ablation methods have been shown to be effective and safe alternatives to hysterectomy for management of DUB. These methods require particular skills and experience and a long learning curve to be performed effectively and safely. Through the past three decades DUB patients in Assiut university hospital were treated with either electrosurgical ablation or hysterectomy. When faced with hysteroscopic challenges during transcervical resection of the endometrium or rollerball coagulation, we used to shift to thermal balloon as backup method . However, expensive uterine balloon could not infrequently be afforded because of financial constrains and limited health resources . Therefore, another method was used as backup for hysteroscopic failures. It was first tried via insulating the conventional double-ended uterine curette then through a specially designed tactile electrosurgical ablation (TEA) probe.The technique of TEA is largely similar to the dilatation and curettage procedure both principally and practically. Hence, the basic requirements for its performance are the general awareness with electrosurgical principles and adequate experience in performing dilatation and curettage. TEA is done by specially designed tactile diathermy probe that carried the job of electrosurgical ablation without hysteroscopy or distension media first in an experimental session that clearly clarified the reproducibility of the depth of thermal damage and safety of the tactile electrosurgical ablator . Thereafter, TEA was successfully performed with satisfactory short and medium term outcomes for ten cases with DUB during an active, relentless bleeding attack. TEA is done under laparoscopic monitoring. The aim of the present work is to present TEA as a simple, inexpensive, novel backup approach for treatment of DUB.