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Uterine Hemorrhage clinical trials

View clinical trials related to Uterine Hemorrhage.

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NCT ID: NCT04915196 Not yet recruiting - Clinical trials for Iron Deficiency Anemia

Tolerability of Iron Therapy in Women With AUB

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

Telephone surveys of female patients using liposomally-bound iron and traditional iron sulphate preparations for the management of iron deficiency anemia to determine gastrointestinal tolerability.

NCT ID: NCT04867109 Recruiting - Clinical trials for Endometrial Neoplasms

HE4 in the Diagnostic Approach of Endometrial Cancer in Patients With Postmenopausal Bleeding

METRODEC
Start date: June 25, 2021
Phase:
Study type: Observational

This study aims to explore the sensitivity of an innovative marker, HE4, in the diagnosis approach of endometrial cancer in case of postmenopausal bleedings.

NCT ID: NCT04766073 Recruiting - Clinical trials for Cesarean Section Complications

Surgical Incision Closure Method to Prevent Niche Formation After Cesarean Section- Randomized Controlled Trial

Start date: July 22, 2021
Phase: N/A
Study type: Interventional

In the last decade we have been exposed to the complication of a caesarean section called a "niche". A niche is an anaerobic defect in the location of the cesarean section, which represents the discontinuity of the endometrium and myometrium. A niche is usually diagnosed by ultrasound, and can also be diagnosed by hysterosalpingogram or hysteroscopy. In the presence of a niche women suffer more frequently from irregular bleeding, dysmenorrhea, chronic pelvic pain, and dyspareunia. We believe that a combination of tissue ischemia and thinning of the scar tissue that forms, causes a niche to form. Large randomized studies regarding the preferred surgical technique in cesarean section, including various methods of incision closure have found that there is no single method that is obviously superior. However, these studies did not examine niche formation as a complication of cesarean section. In this study we will examine whether a unique incision closure method reduces post-cesarean niche formation.

NCT ID: NCT04710017 Completed - Uterine Bleeding Clinical Trials

Tranexamic Acid and Depot-Medroxyprogesterone Acetate for Perimenopausal Irregular Uterine Bleeding

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

Abnormal uterine bleeding is a symptom and not a disease. It is one of the most frequently encountered complaints in gynecologic practice. It accounts for more than 70% of all gynecological consultations in the peri- and post-menopausal age group. Abnormal uterine bleeding may be acute or chronic and is defined as bleeding from the uterine corpus that is abnormal in regularity, volume, frequency, or duration and occurs in the absence of pregnancy. Chronic heavy or prolonged uterine bleeding can result in anemia, interfere with daily activities. Iron deficiency anemia develops in 21 to 67 percent of cases and raises concerns about uterine cancer. According to the International Federation of Obstetrics and Gynecology, the classification of abnormal uterine bleeding is based on PALM-COEIN which is an acronym for various etiologies namely polyp, adenomyosis, leiomyoma, malignancy and hyperplasia, coagulopathy, ovulatory dysfunction, endometrial disorders, iatrogenic and not otherwise classified (PALM-COEIN).

NCT ID: NCT04676061 Terminated - Contraception Clinical Trials

Effects of a Progestin on Frequent and/or Prolonged Bleeding With Nexplanon™

Start date: February 11, 2021
Phase: Phase 4
Study type: Interventional

Effects of norethindrone acetate (NTA) in patients with Nexplanon.

NCT ID: NCT04637022 Recruiting - Uterine Fibroid Clinical Trials

4K Versus 3D Laparoscopic Colporraphy by Surgeons in Training: a Prospective Randomized Trial

Start date: January 25, 2021
Phase:
Study type: Observational

This prospective randomized trial aims to assess if the operative time of vaginal cuff suture performed by trainees could be reduced using 3D laparoscopy instead of 4K laparoscopy.

NCT ID: NCT04612881 Recruiting - Vaginal Bleeding Clinical Trials

Fitostimoline Vaginal Pessaries in Women With Hysterectomy. Randomized, Perspective, Monoscentric Study.

Start date: October 18, 2020
Phase:
Study type: Observational

Clinical evaluation of Fitostimoline vaginal pessaries in the treatment of hysterectomy. An observational, randomized, perspective study performed on 60 women where 30 women are treated with fitostimoline pessaries and 30 women are treated with the standard of care.

NCT ID: NCT04579965 Not yet recruiting - Clinical trials for Dysfunctional Uterine Bleeding

Misotac vs Combined Oral Contraceptive Pill in the Treatment of Symptomatic Isthmocele

Start date: October 1, 2020
Phase: N/A
Study type: Interventional

Isthmocele is a growing concern as a cause of abnormal uterine bleeding, especially post menstrual bleeding which may be present in up to 82% of these cases (Iannone et al 2019). our trial is a randomized clinical trial in which women will be randomly allocated to either medical treatment by oral contraceptive or to medical treatment by misotac.

NCT ID: NCT04528108 Completed - Clinical trials for Dysfunctional Uterine Bleeding

Chinese Medicine Periodic Therapy for Dysfunctional Uterine Bleeding During Adolescence With Yin Deficiency and Blood Heat Syndrome

Start date: September 2, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to conduct a randomized, single blind, controlled intervention trial to observe the therapeutic effect of kidney-tonifying and tune up Chong-Ren hemostasis Chinese medicine periodic therapy for dysfunctional uterine bleeding based on objective Chinese and western medicine evaluation standard.

NCT ID: NCT04475497 Terminated - Clinical trials for Abnormal Uterine Bleeding

Role of Blood Management in Perioperative Outcomes

Start date: July 24, 2020
Phase: N/A
Study type: Interventional

There is currently limited information regarding the role of blood management in the benign gynecologic population and specifically, in patients who are scheduled to undergo surgery for fibroids and/or abnormal uterine bleeding. A thorough search through PubMed and clinicaltrials.gov did not reveal any studies on this issue. In 2019 at CCF only 2% of gyn patients at Main Campus were referred to blood management, but 12.6% of the main campus gyn population had a Hb of <10.0 g/dL. The overall goal of this study is to evaluate the role of preoperative blood management in optimizing surgical outcomes by reducing the co-morbidities associated with postoperative blood transfusion.