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Tissue Adhesions clinical trials

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NCT ID: NCT04232592 Not yet recruiting - Clinical trials for Intrauterine Adhesion

Clinical Safety Study of Human Embryonic Stem Cell Derived Mesenchymal Cells in the Treatment of Moderate and Severe Intrauterine Adhesions

Start date: January 2020
Phase: Phase 1
Study type: Interventional

To observe the clinical safety of intrauterine injection of human embryonic stem cell derived mesenchymal cells in the treatment of moderate and severe intrauterine adhesion, and to preliminarily explore its clinical effectiveness in promoting endometrial regeneration and repair.

NCT ID: NCT04077606 Not yet recruiting - Clinical trials for Gingival Inflammation

Gingival Inflammatory Response,Bacterial Adhesion and Patient Satisfaction of Ceramo-metallic vs Zirconia Crowns

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

Ceramo metallic restoration has proved high success rate over past years as considered to be the gold standard while Monolithic zirconia as fixed dental prostheses have gained attention because of their good fracture strength, low wear of the enamel antagonist and pleasant color .Material composition will affect gingival health and biofilm formation which initiate caries and periodontal diseases.

NCT ID: NCT04030273 Not yet recruiting - Myoma;Uterus Clinical Trials

Prevalence of Intrauterine Adhesions After Abdominal Myomectomy

Start date: January 2022
Phase:
Study type: Observational

Uterine fibroids are the most common benign tumors of the genital organs of women of childbearing age. Literature data show that more than 75% of women have fibroids.Symptomatic fibroids account for approximately over 200,000 hysterectomies and 50,000 myomectomies annually in the United States. Fibroids have a major impact on fertility, with significant adverse effect on implantation rate and spontaneous abortion rates when compared with infertile women without fibroids. The definitive treatment for uterine fibroids in a fertile patient is surgical excision. Although usually effective, myomectomy is not a risk-free operation, since the surgical procedure can cause mechanical infertility and can be associated with infection, injury to adjacent tissues, hemorrhage and need to convert to hysterectomy. A not often mentioned consequence of myomectomy is post-operative intrauterine adhesion formation. It has been reported that 50% of women undergoing open myomectomy are found to have intrauterine adhesions diagnosed by hysteroscopy performed 3 months after surgery. Such a high prevalence of intrauterine adhesions after open myomectomy is unexpected, however only few studies have addressed this topic. It is accepted that injury to the endometrium is generally considered to be the primary causative factor for the development of intrauterine adhesions. The reason for such a high incidence of intrauterine adhesions after open myomectomy is unclear. It is speculated that infection or in adverted closure of the uterine cavity may play a role in intrauterine adhesion formation. The relationship between the number of fibroids removed and the risk of adhesions suggests a traumatic etiology. In the preservation of the uterus for the purpose of fertility, it is essential to also understand the impact of myomectomy on the endometrium. Currently no guideline recommends in office hysteroscopy as follow-up after myomectomy. The purpose of the present study is to evaluate the frequency of uterine adhesions following myomectomy and the impact of number, size and location of the fibroids as well as intraoperative breach of the endometrial cavity at the time of the myomectomy.

NCT ID: NCT03800511 Not yet recruiting - Clinical trials for Intra-Abdominal; Adhesion

Prediction of Intra-abdominal Adhesion Before CS

Start date: March 2019
Phase:
Study type: Observational

Recognition of intraabdominal adhesion before doing repeated cesarean section is helpful for the surgeon and patients.

NCT ID: NCT03629132 Not yet recruiting - Clinical trials for Intrauterine Adhesion

PRP Prevents Recurrence of Intrauterine Adhesions

RPR-IUAs
Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Effect of platelet-rich plasma (PRP) on uterine scar fibrosis, endometrial receptivity and pregnancy outcome in patients with severe intrauterine adhesions

NCT ID: NCT03183362 Not yet recruiting - Cesarean Section Clinical Trials

Comparison of Barbed and Conventional Sutures in Adhesion Formation Following Cesarean Section

Start date: August 2017
Phase: N/A
Study type: Interventional

The aim of this randomized controlled trial is to determine whether the use of barbed sutures to close uterine incision at cesarean section is associated with more postoperative adhesions compared with conventional sutures or not.

NCT ID: NCT03013582 Not yet recruiting - Fibrosis Clinical Trials

Amniotic Membrane Wrapping and Tenolysis Versus Tenolysis Alone for Treatment of Tendon Adhesions of the Hand/Wrist

Start date: January 2017
Phase: N/A
Study type: Interventional

Tendon adhesions of the hand remain a ubiquitous problem facing hand surgeons and hand therapists alike. Despite their commonality, no consensus exists as to the best means of preventing adhesions, or the most ideal methods to treat them once they have occurred. The purpose of this study is to compare patient outcomes after standard operative tenolysis performed for adhesions of the hand to outcomes after tenolysis with the use of allograft human amniotic membrane.

NCT ID: NCT02847676 Not yet recruiting - Clinical trials for Peritoneal Adhesions

Differences in Peritoneal Stem Cells in Women With and Without Adhesions After Gynaecological Surgery

Start date: August 2016
Phase: N/A
Study type: Observational [Patient Registry]

Our study aims to characterise a possible pluripotent cell population in the abdomen responsible for peritoneal adhesions. We therefore want to take samples from women undergoing planned laparoscopic surgery with and without adhesions, isolate the cells and characterise them for markers of pluripotency.

NCT ID: NCT02790177 Not yet recruiting - Clinical trials for Post Operative Adhesions

Role of Hyaluronic Acid in the Prevention of Post-operative Adhesions: a RCT

HiB
Start date: June 2016
Phase: Phase 3
Study type: Interventional

The objective of study is to determine the effect of hyaluronic acid on the formation of post-operative adhesions. It will be a randomized control trial comparing the product against normal saline.

NCT ID: NCT02617108 Not yet recruiting - Uterine Septum Clinical Trials

Intrauterine Balloon and Postoperative Estrogen Therapy in the Prevention of Adhesion Reformation After Hysteroscopic Adhesiolysis

Start date: December 2019
Phase: N/A
Study type: Interventional

Patients who want to go TCRS will randomly divided 3 groups. In Group 1(100 patients), women received postoperative estrogen therapy. In Group 2 (100 patients), a Foley catheter with the balloon inflated with 4 ml of normal saline solution will be placed into the uterine cavity at the end of the operation for five days. In Group 3 (110 patients), women will not receive any of the treatment (comparison group). All subjects underwent two further hysteroscopy, one and three months after the initial surgery. At the second or third look hysteroscopy, the incidence of intra-uterine adhesion will be analyzed.