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Hysteroscopy clinical trials

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NCT ID: NCT05069077 Not yet recruiting - Hysteroscopy Clinical Trials

the Effect of Music on Pain and Women Satisfaction During Diagnostic Outpatient Hysteroscopy in Postmenopausal Women

Start date: October 15, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate the value of music in diagnostic outpatient hysteroscopy on patients' level of pain and satisfaction in postmenopausal women

NCT ID: NCT05069025 Not yet recruiting - Hysteroscopy Clinical Trials

Use of Music in Reducing Pain During Outpatient Hysteroscopy in Primarily Infertile Patients

Start date: October 10, 2021
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate the value of music in outpatient hysteroscopy on patients' level of pain and satisfaction in primarily infertile patients.

NCT ID: NCT04862598 Recruiting - Clinical trials for Patient Satisfaction

Virtual Reality to Improve Satisfaction in Hysteroscopy Patients

VIP
Start date: March 24, 2021
Phase: N/A
Study type: Interventional

This study aims to investigate whether viewing an immersive virtual reality (VR) image through a VR headset during elective hysteroscopy under Registered Nurse (RN) led sedation with fentanyl and midazolam plus local anesthesia (monitored anesthetic care) will improve patient satisfaction with their anesthesia. Patients will be randomized to either receive usual care or usual care plus VR. Satisfaction will be measured by asking patients to complete a post-procedure survey consisting of 11 questions.

NCT ID: NCT04597463 Completed - Hysteroscopy Clinical Trials

The Combination of Endometrial Injury and Freeze All Strategy in Women With a History of RIF

Start date: December 2, 2017
Phase: N/A
Study type: Interventional

The investigators checked the hypothesis whether endometrial injury performed during the cycle before a frozen embryo transfer in women with RIF can improve pregnancy rates

NCT ID: NCT04462835 Completed - Hysteroscopy Clinical Trials

Feasibility, Effectiveness and Safety of Outpatient Hysteroscopy

FESHA
Start date: May 1, 2020
Phase:
Study type: Observational

Study Objective: The main objective of the study is to assess the feasibility, effectiveness and safety of outpatient hysteroscopies performed in our Office Hysteroscopy Unit. Design: Retrospective observational study of prospectively collected data from the Office Hysteroscopy Unit database. Setting: Tertiary care university hospital Patients: Three thousand patients who consecutively attended an ambulatory hysteroscopy in our centre from may 2008 to october 2019 Interventions: The Office hysteroscopy was performed with several rigid 5-6 mm diameter devices when indicated with a diagnostic and/or therapeutic purpose

NCT ID: NCT04232930 Completed - Hysteroscopy Clinical Trials

The Use of Music in Reducing Pain During Outpatient Hysteroscopy

Start date: June 1, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to demonstrate the value of music in outpatient hysteroscopy on patients' level of pain and satisfaction. This may have a role in our daily practice in providing a better patient care in outpatient hysteroscopy.

NCT ID: NCT04166500 Completed - Hysteroscopy Clinical Trials

Early Outpatient Hysteroscopy Can Prevent Intrauterine Adhesion After Induced Abortion

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Background: Intrauterine adhesions are a difficult clinical problem for reproductive infertility. The most common cause is uterine cavity surgery and post-abortion (including abortion and spontaneous abortion). After the abortion, the uterine cavity adhesion, when is the key point, the literature is not much ink, early literature has mentioned that after the abortion, the uterus scraping action is scraped in four days and the uterine adhesion will be smaller than one to four weeks. Much more, it seems that the sooner the uterine adhesion factor is excluded, the more it can reduce uterine adhesion, but the uterine curettage itself is a risk factor for uterine adhesion. This early practice, the current clinical application, is not used, Instead, it is a hysteroscopy. Our past clinical observations, as soon as possible after the abortion, outpatient hysteroscopy, can find the tissue factors that may cause adhesion in the uterine cavity as soon as possible, and immediately remove it with an outpatient hysteroscope. Objective: To verify the early outpatient hysteroscopy and reduce the occurrence of intrauterine adhesion after abortion. Expected benefits to patients: Abortion is likely to cause intrauterine adhesions, which may further cause the incidence of reproductive infertility, should be involved before the formation of permanent injury, reduce the adhesion of the uterine cavity. Outpatient hysteroscopy is a simple and easy-to-use examination procedure that is painless and does not require anesthesia. Although it is invasive but has few complications, it is expected to reduce the occurrence of intrauterine adhesion after abortion.

NCT ID: NCT04096677 Recruiting - Hysteroscopy Clinical Trials

Effects of Hysteroscopy and Transvaginal Surgery on Reproductive Prognosis in Patients With Post Cesarean Scar Defect

Start date: January 1, 2017
Phase:
Study type: Observational [Patient Registry]

The study is to compare hysteroscopic repair and transvaginal intervention for correcting uterine defect in patients with post cesarean scar defect (PCSD) and the reproductive prognosis.

NCT ID: NCT04042974 Not yet recruiting - Hysteroscopy Clinical Trials

Vaginal Dinoprostone Prior to Diagnostic Office Hysteroscopy in Primarily Infertile Patients

Start date: August 10, 2019
Phase: Phase 4
Study type: Interventional

To compare the effectiveness of vaginal dinoprostone with placebo in minimizing the pain experienced by primarily infertile patients during diagnostic office hysteroscopy and to assess the ease of insertion of hysteroscope as reported by the hysteroscopist.

NCT ID: NCT03880435 Active, not recruiting - Infertility Clinical Trials

HYALOBARRIER® GEL ENDO Versus no HYALOBARRIER® GEL ENDO Following Operative Hysteroscopy for Improving Reproductive Outcome in Women With Intrauterine Pathology Wishing to Become Pregnant

AGNOHSTIC
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

To compare the costs and effects of HYALOBARRIER® GEL ENDO versus no HYALOBARRIER® GEL ENDO for increasing the chance of conception leading to live birth measured at 30 weeks after randomization in women wishing to become pregnant after surgical removal of intrauterine pathology (endometrial polyps, fibroids with uterine cavity deformation, uterine septa, IUAs or RPOC after miscarriage) by hysteroscopy as an outpatient or in hospital treatment.