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Abnormal Uterine Bleeding clinical trials

View clinical trials related to Abnormal Uterine Bleeding.

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NCT ID: NCT03130387 Completed - Clinical trials for Abnormal Uterine Bleeding

Prevalence of Cesarean Section Niche in Women With Unexplained Abnormal Uterine Bleeding

Niche
Start date: January 1, 2016
Phase: N/A
Study type: Interventional

Prevalence of Cesarean Section Niche in women With Unexplained Abnormal Uterine Bleeding

NCT ID: NCT02192606 Completed - Uterine Fibroids Clinical Trials

Does 3D Laparoscopy Improve Vaginal Cuff Suture Time?

3DRCT
Start date: November 2013
Phase: Phase 1
Study type: Interventional

The objective aim is to evaluate whether the use of 3D laparoscopy facilitates the vaginal cuff closure of the vaginal cuff during a total laparoscopic hysterectomy among novice laparoscopists (PGY 2-4, Fellow). This is a randomized single blinded controlled trial comparing the difference in 2D vs. 3D in regards to vaginal cuff closure time stratified by residents and fellows. Patients will undergo a total laparoscopic hysterectomy and will be randomized to either 2D versus 3D.

NCT ID: NCT02029144 Completed - Clinical trials for Abnormal Uterine Bleeding

Observational Study of Dydrogesterone in Cycle Regularization

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

Dydrogesterone has been widely used worldwide for various gynecological and obstetric indications: - Dydrogesterone is effective in cycle regulation treatment. - Dydrogesterone is recognized as none interference to hypothalamus pituitary ovary (HPO) axis in the recommended dosage. - Dydrogesterone might have non-negative effect on glucose and lipid metabolic.

NCT ID: NCT02002260 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 levonorgestrel intrauterine system (LNG-IUS) to combined oral contraceptives (COCs) for treatment of heavy menstrual bleeding. This study is designed to be conducted within the context of a patient's standard/usual/typical care from their primary gynecologic care provider. We hypothesize that, compared to COCs, the LNG-IUS will be more effective at improving bleeding-related quality of life and will be associated with fewer treatment failures and greater cost-effectiveness at one year. To test these hypotheses, we plan to enroll 59 women from several sites who present for gynecologic care and self-report heavy menstrual bleeding into a RCT comparing LNG-IUS to COCs. The eligible study population includes women with heavy menstrual bleeding secondary to ovulatory disorders (AUB-O) or endometrial hemostatic disorders (AUB-E). Women meeting study eligibility will be randomized to receive LNG-IUS or COCs. Main study outcomes will be obtained at 6 weeks, 3 months, 6 months, and 1 year.

NCT ID: NCT01908738 Completed - Clinical trials for Abnormal Uterine Bleeding

Effectiveness of Paracervical Block Versus Lidocaine Spray During Endometrial Biopsy

Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study to determine effectiveness of paracervical block, lidocaine spray and only oral analgesic drugs for pain relief during endometrial biopsy.

NCT ID: NCT01786798 Recruiting - Clinical trials for Abnormal Uterine Bleeding

Transvaginal Ultrasound in Women With Abnormal Uterine Bleeding

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

The objective of this study is to investigate the role of transvaginal ultrasound in detecting endometrial hyperplasia and endometrial cancer in women aged more than 35 presenting with abnormal uterine bleeding.

NCT ID: NCT01721304 Completed - Clinical trials for Abnormal Uterine Bleeding

Decisionmaking for Abnormal Uterine Bleeding (AUB)

Start date: May 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if using a computer survey about preferences for treatment of abnormal uterine bleeding (AUB) is useful and if it will improve patient satisfaction with clinical care and decision making. This study is a two-part study. The first pilot tests the computerized tool to ensure it is understood by patients, then the second part is a randomized study (computerized tool versus usual care) to see if improvements are made in satisfaction and if there are reductions in decision regret.

NCT ID: NCT01289314 Recruiting - Dysmenorrhea Clinical Trials

Long Term Outcomes Following Total Laparoscopic Hysterectomy and Laparoscopic Supracervical Hysterectomy

Start date: February 2011
Phase: N/A
Study type: Interventional

Objective: To compare the occurrence and intensity of pelvic pain as well as patient satisfaction and quality of life after total laparoscopic and laparoscopic supracervical hysterectomy. Design: Prospective randomised trial. Null hypothesis 1: There is no significant difference in occurrence and intensity of pelvic pain following TLH compared with following LSH. Null hypothesis 2: There is no significant difference in patient satisfaction and quality of life following TLH compared with following LSH.

NCT ID: NCT01026805 Completed - Infertility Clinical Trials

Clinical Evaluation of the Interlace Medical Hysteroscopic Morcellator

Start date: February 2009
Phase: N/A
Study type: Observational

This study assesses the effectiveness of intrauterine fibroid and polyp removal using the Interlace Medical 1st generation hysteroscopic morcellator device based on a retrospective review of medical records of women who have been treated with the device.

NCT ID: NCT00755651 Completed - Clinical trials for Abnormal Uterine Bleeding

Studies on the H Pipelle, a New Device for Endometrial Sampling at Hysteroscopy

Start date: January 2003
Phase: N/A
Study type: Interventional

The investigators have developed a novel instrument for taking endometrial biopsies at no touch (vaginoscopic) hysterectomy which avoids the need to instrument the vagina with speculums and tenaculums, and also avoids the possible need for cervical dilatation. The investigators wish to study the ease of use and efficacy of the new device compared with traditional techniques of endometrial sampling at hysteroscopy.