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Uterine Diseases clinical trials

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NCT ID: NCT03748238 Recruiting - Infertility Clinical Trials

Endometrial Injury In Recurrent Implantation Failure

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to investigate that the efficacy of the endometrial injury before IVF in recurrent implantation failure patients.

NCT ID: NCT03289468 Recruiting - Clinical trials for Endometrial Diseases

Study of Diagnosis of Color Power Doppler Combined Minimally Invasive Sampling for Endometrial Diseases

Start date: July 10, 2017
Phase:
Study type: Observational

The postmenopausal women with vaginal bleeding were selected in this cross-sectional study. The basic characteristics information and endometrial blood flow energy index of endometrium were detected by color power Doppler ultrasound, and the energy histogram of endometrium was obtained. The specimen of uterine cytology and endometrial tissue were obtained through minimally invasive endometrium sampler, which were diagnosed by pathology. The statistical data were used to detect endometrial and precancerous lesions to observe the endpoint, and to provide the energy histogram model of the early warning endothelial diseases.

NCT ID: NCT02914704 Recruiting - Uterine Fibroids Clinical Trials

Treatment of Benign Uterine Disorders Using High Intensity Focused Ultrasound (MR-HIFU)

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

MRI-guided high intensity focused ultrasound (MRI-HIFU) has been proven to be a safe and effective method in treating uterine fibroids and also adenomyosis. However, systematic studies on the effect of this treatment on factors affecting fertility are still lacking. Also quite little is known about body's systemic response to MRI-HIFU. Thus the aim of this study is to obtain more information on the systemic response of the body to the HIFU-treatment when treating non-malignant disease as well as to study the effect of MRI-HIFU on factors affecting fertility. Women with symptomatic uterine fibroids or adenomyosis suitable for MRI-HIFU treatment are recruited to this study. The severity of symptoms will be assessed with UFS-QoL and the same questionnaire will also be used in follow-up 3, 6 and 12 months after treatment. Blood, urine and endometrium samples will be collected pre- and postoperatively and during follow-up 3, 6 and 12 months after the treatment. From these samples detailed analysis of the immunological, inflammatory and hormonal response will be performed. As this is the first study in Finland of treating uterine fibroids and adenomyosis using MRI-HIFU, also a report about the efficacy of the MRI-HIFU in treating the uterine disorders will be published, and a key tool in assessing the treatment outcome would be the UFS-QoL questionnaire. Also new methods for improving patient selection as well as treatment efficacy will be evaluated in this study.

NCT ID: NCT02691715 Recruiting - Endometrial Disease Clinical Trials

Intrauterine Saline Washing for Detection Endometrial Disease in Patients With Abnormal Uterine Bleeding

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

Investigator will examined the diagnostic effect of the endometrial washing by saline. Because this technique more less painful and easier compared to endometrial curettage. Participants will separate into two groups. In study groups before endometrial curettage 5 cc saline infused to the endometrial cavity then aspirate and put into thin prep to examined. After this procedure routine endometrial curettage will be done. In control group only endometrial curettage will be done. Pathologic results of thin prep and curettage will compared.

NCT ID: NCT02367703 Recruiting - Clinical trials for Benign Uterine Diseases

Feasibility and Benefit of Laparoscopic Hysterectomy With Less Than 3 Millimeter Diameter's Instruments in Current Practice

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

Hysterectomy for benign uterine disease is often intended to young perimenopausal patients. Currently laparoscopic hysterectomy is commonly used in this indication. We are wondering if decreasing the diameter of laparoscopic instruments could reduce postoperative pain and improve esthetic result without increasing operative time. The purpose of the study is to improve patients' care.