Clinical Trials Logo

Infertility of Tubal Origin clinical trials

View clinical trials related to Infertility of Tubal Origin.

Filter by:
  • Completed  
  • Page 1

NCT ID: NCT05209542 Completed - Clinical trials for Infertility of Tubal Origin

Hysterosalpingo-Foam Ultrasonography Combined With Power Doppler, Compared With Laparoscopy in Tubal Patency Assessment in Cases of Infertility

Start date: February 9, 2018
Phase: N/A
Study type: Interventional

Women presenting with primary or secondary infertility and are undergoing investigation of tubal patency assessment will be subjected to: - The examination is performed between days 5 and 10 of the menstrual cycle. - Routine antibiotic prophylaxis using oral Azithromycin the day before and routine administration of NSAID rectal suppository one hour before the procedure - Initially, real-time 2D +/- 3D vaginal ultrasound assessment of the pelvis - The cervix is to be visualized with a Cusco speculum and to be cleaned with an antiseptic then A No. 5 pediatric Foley catheter will be introduced into the cervical os, using a tenaculum if necessary. The balloon is to be positioned in the lower uterine cavity and to be inflated with 2 ml of saline to prevent backflow of contrast medium through the cervix then the speculum will be removed and the vaginal transducer is going to be reintroduced in the longitudinal plane to confirm correct placement of the catheter. - Initial 3-5 ml of foam contrast is to be introduced slowly into the endometrial cavity while the flow of contrast medium in each tube is evaluated using grayscale and power Doppler imaging - Power Doppler is very helpful to confirm the direction of the flow as well as the acceleration during injection. - Tubal patency and quality of visualization are classified according the following parameters: 1. Flow over the whole length of the tube, fimbrial outflow or peritoneal spillage of contrast provided definite evidence of complete (i.e. proximal and distal) tubal patency. 2. Paracornual flow only without visualization of fimbrial outflow or peritoneal spillage suggests at least proximal patency. 3. Contrast filling of the endometrial cavity without cornual flow suggests possible tubal occlusion. 4. Technical difficulty making tubal evaluation impossible - Standard laparoscopic evaluation with the dye test (methylene blue staining) is to be performed 1 day after ultrasound tests with 1 day of hospitalization under general anesthesia.

NCT ID: NCT04077242 Completed - Infertility, Female Clinical Trials

Hysteroscopic Evaluation of Fallopian Tubal Patency

Start date: May 31, 2019
Phase: N/A
Study type: Interventional

Hysteroscopy is an important tool in the evaluation of sterility. Assessing tubal patency during hysteroscopy seems highly relevant, particularly when it allows for a low cost, fast, gentle, and accurate way of gathering information that may guide clinical care. Therefore, it is important to know which technique is the best. Thus, the primary aim of this study is to evaluate the reliability of (1.) the hysteroscopic visualization of a "tubal flow" and (2.) the "Parryscope technique" as compared to the gold standard, namely laparoscopic chromopertubation. In a prospective, randomized study, the following women are enrolled: (1.) The patient is subfertile, defined as being unable to become pregnant within a year despite unprotected sexual intercourse. It is also within the standard of care to be presumed subfertile if one has tried for six months and has known risk factors that would hinder conception, including but not limited to anovulation and endometriosis. (2.) A concurrent diagnostic hysteroscopy and laparoscopy with chromopertubation are performed at the Clinical Division of Gynecological Endocrinology and Reproductive Medicine at the Medical University of Vienna. Hysteroscopic evaluation of tubal patency (either by a positive "tubal flow" or a visible flow of air bubbles in the "Parryscope technique") and the result of the laparoscopic chromopertubation (tubal patency existing or not existing) will be the primary outcome parameters. A total 60 patients are enrolled (30 patients in the "flow assessment" group, 30 patients in the "Parryscope" group) and randomization is performed as block randomization in 4 blocks.