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Uterine Hemorrhage clinical trials

View clinical trials related to Uterine Hemorrhage.

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NCT ID: NCT06293066 Active, not recruiting - Endometrial Cancer Clinical Trials

Performance of Ultrasound in Women With Postmenopausal or Abnormal Uterine Bleeding Between White and Black Ethnic Groups- a Retrospective Cohort Study.

Start date: January 31, 2024
Phase:
Study type: Observational

Primary Objective: To assess whether there is a higher incidence of uninformative ultrasound in black vs white women

NCT ID: NCT05474703 Active, not recruiting - Clinical trials for Abnormal Uterine Bleeding

Evaluation of the Effects of Levonorgestrel-releasing Intrauterine Device and Dydrogestreone on Quality of Life and Sexual Life in Patients With Abnormal Uterine Bleeding.

Start date: February 20, 2022
Phase:
Study type: Observational [Patient Registry]

This study was retrospectively collected from patients who were diagnosed with abnormal uterine bleeding and received oral dydrogesterone therapy for at least six months or who were administered an intrauterine device containing levonorgestrel at least six months ago, and prospectively Short form 36 (P-36); It covers the comparison of the Quality of Life Scale and the Female Sexual Function Scale (FSFI) by asking over the phone.

NCT ID: NCT05299801 Active, not recruiting - Clinical trials for Abnormal Uterine Bleeding

DAta MIning to Evaluate Novasure Treatment

DAMIEN
Start date: July 1, 2021
Phase:
Study type: Observational

Abnormal Uterine Bleeding (AUB) is a common health problem that affects approximately 30% of women of reproductive age and can have several underlying causes. It significantly affects quality of life, use of medical resources and health costs. Endometrial ablation is a commonly used minimally invasive surgical procedure for the treatment of AUB that destroys endometrial tissue. This procedure is an alternative treatment to hysterectomy because it is less invasive and has a shorter recovery period. Several ablation techniques are available to remove endometrial tissue, including bipolar radiofrequency (NovaSure treatment). While patient satisfaction with this form of endometrial ablation for the treatment of AUB is high, approximately 10-20% of women undergoing endometrial ablation require additional invasive surgery, primarily because of persistent blood loss or pain. There is therefore a need to identify and evaluate factors that can improve women's outcomes, or that can be building blocks for prognostic models that can be used to influence clinical practice. In this 10-year single-center retrospective cohort study, we aim to apply data mining and machine learning techniques to uncover hidden relationships/patterns between variables, and identify factors and patients at increased risk for Novasure treatment failure. With multiple time variables, this is not possible with a simple statistical analysis. Discovering these patterns and risk factors could help improve medical care, patient counseling and patient satisfaction.

NCT ID: NCT04434066 Active, not recruiting - Surgery Clinical Trials

Outcomes on Abdominal Versus Vaginal Morcellation At Time of Hysterectomy

Start date: January 8, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to investigate differences in perioperative and postoperative outcomes between the abdominal (AM) versus vaginal (VM) routes of contained morcellation in participants undergoing laparoscopic total hysterectomies in a randomized controlled trial.

NCT ID: NCT04267562 Active, not recruiting - Menorrhagia Clinical Trials

Minitouch Endometrial Ablation System Treatment for Menorrhagia: An Evaluation of Safety & Effectiveness

Start date: February 28, 2020
Phase: N/A
Study type: Interventional

The EASE Clinical Trial is prospective, multi-center, single-arm (open-label), non-randomized, clinical trial to evaluate the Minitouch Endometrial Ablation System ("Minitouch System") in premenopausal women with menorrhagia.

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: 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: NCT02103764 Active, not recruiting - Clinical trials for Dysfunctional Uterine Bleeding

Efficacy of Cyclic DSG Compared With Cyclic MPA for the Treatment of Anovulatory DUB

SI-AUB-RCT
Start date: August 2013
Phase: Phase 3
Study type: Interventional

The objectives of the present study is to determine the effectiveness of cyclic desogestrel (DSG) compared with cyclic medroxyprogesterone acetate for the treatment of anovulatory dysfunctional uterine bleeding (DUB) in the following aspects: 1. Endometrial histopathology changes 2. Menstrual cycle control.

NCT ID: NCT02002260 Active, not recruiting - Clinical trials for Abnormal Uterine Bleeding

Stopping Heavy Periods Project

SHiPP
Start date: February 2013
Phase: N/A
Study type: Interventional

This study is a randomized clinical trial comparing the effectiveness of the levonorgestrel intrauterine system (LNG-IUS) to combined oral contraceptives (COCs) for improving quality of life among women who report heavy menstrual bleeding.

NCT ID: NCT01979861 Active, not recruiting - Menorrhagia Clinical Trials

Safety & Effectiveness Study of AEGEA Vapor System to Treat Excessive Uterine Bleeding

Start date: February 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if the AEGEA Vapor System for endometrial ablation is safe and effective for reducing menstrual blood loss in women with excessive uterine bleeding (menorrhagia)