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Intrauterine Adhesion clinical trials

View clinical trials related to Intrauterine Adhesion.

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NCT ID: NCT02744716 Completed - Clinical trials for Intrauterine Adhesion

Effects of Aspirin on Uterine Endometrial Repair Severe Intrauterine Adhesion

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

This study aimed To investigate the effects of estrogen in combination with aspirin and intrauterine balloon on the uterine endometrial repair and reproductive prognosis in patients after surgery for severe intrauterine adhesion .

NCT ID: NCT02220621 Completed - Clinical trials for Intrauterine Adhesion

Efficacy and Safety of Crosslinked Hyaluronan Gel for Preventing Intrauterine Adhesion

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

Intrauterine adhesion (IUA) is the adhesion of intrauterine tissues due to the exposure of myometrial tissues caused by the endometrial basal injury. IUA is clinically manifested as symptoms such as abdominal pain, hypomenorrhea or amenorrhea, sterility and habitual abortion, which seriously affect the patients quality of life. Preventing IUA has been tried using different methods such as barrier or stent in order to separate the opposing endometrium during the tissue healing processes. Although some successes have been reported there are still some challenges need to be dealt with. One of the barrier materials for preventing IUA is made of hyaluronic acid (HA). HA is a natural ECM of human tissue with excellent biocompatibility and promotes the scar-free wound repair. The self-crosslinked esterified HA gel has demonstrated the capacity to prevent IUA in clinical studies. A novel self-crosslinked HA gel is developed by BioRegen Biomedical(Changzhou)Co., Ltd with proprietary technologies. This product is a highly viscoelastic crosslinked gel that overcomes the shortcoming of sodium hyaluronate with high motility and too quick degradation in vivo. For this product, the results of animal experiments and various safety features have been designed and tested conforming to the national regulations and standards. In order to launch this product to the market, this prospective, randomized and controlled clinical trial is designed and will be performed to verify its safety/efficacy.

NCT ID: NCT01167296 Completed - Clinical trials for Intrauterine Adhesion

Safety of Leaving Cook Balloon Uterine Stent in Uterus for One Month

Start date: July 2010
Phase: Phase 4
Study type: Interventional

To use Cook balloon uterine stent to prevent intrauterine adhesion (IUA), and to see if leaving it in the uterus will cause uterine infection.