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Tissue Adhesions clinical trials

View clinical trials related to Tissue Adhesions.

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NCT ID: NCT04672421 Completed - Laparoscopy Clinical Trials

The Efficacy and Safety of Medicurtain® in Patients With Total Laparoscopic Hysterectomy (Pivotal Study)

Start date: April 18, 2011
Phase: N/A
Study type: Interventional

This study was designed to assess the safety and efficacy of MEDICURTAIN. Patients who underwent total laparoscopic hysterectomy were randomly assigned either into Medicurtain® treatment group or non-treatment control group. Adhesion formations at 8 weeks after the index surgery were compared between the two groups by using the well-defined grade scale and image recording.

NCT ID: NCT04669756 Completed - Surgery Clinical Trials

Ovariopexy for Adhesion Prevention After Laparoscopic Removal of Endometriosis of the Pelvic Side Wall or the Ovary

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

prospective randomized Trial comparing ovariopexy over 2, 4 or 6 days vs Placebo after surgery because of endometriosis of the pelvic side wall or the ovary or both

NCT ID: NCT04638855 Completed - Clinical trials for Tissue Adhesion, Surgery-Induced

The Efficacy and Safety of Medicurtain® in Patients With Hysteroscopy (Pivotal Study)

Start date: September 8, 2010
Phase: N/A
Study type: Interventional

This study was designed to assess the safety and efficacy of MEDICURTAIN, an adhesion barrier in patients who underwent hysteroscopy with uterine polyp or endometrial myoma or missed abortion (uterine lesion suspected to be associated with pregnancy) or intrauterine adhesion. Adhesion formation in both groups was evaluated by the grading scale and photographs taken during the follow up to evaluate the safety and efficacy of the product.

NCT ID: NCT04381728 Completed - Clinical trials for Intrauterine Adhesion

PREvention of Intrauterine Adhesion After Hysteroscopic Surgery With Novel deGradable Film

PREG1
Start date: November 18, 2019
Phase: N/A
Study type: Interventional

Intrauterine adhesions (IUA) are the major long-term complication of intrauterine procedures and are associated with pelvic pain, menstrual disorders, obstetrical complication and infertility. Womed Leaf is a medical device specifically designed for intrauterine use that prevents intra-uterine adhesions. It is a film that acts as a mechanical barrier to keep uterus walls separated during healing. It is then naturally discharged through the cervix and vagina in less than 30 days. The PREG1 clinical investigation is designed to evaluate Womed Leaf safety under clinical conditions, in women scheduled for a hysteroscopic myomectomy as well as its efficacy.

NCT ID: NCT04320173 Completed - Healthy Clinical Trials

Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Lidocaine Patch 5% and Lidocaine Medicated Plaster 5% in Healthy, Adult, Human Subjects

Start date: February 14, 2017
Phase: Phase 1
Study type: Interventional

The primary objective of this study was to evaluate the adhesion performance of ZTlido® (lidocaine topical system) 1.8% compared to adhesion performance for Lidoderm® (lidocaine patch 5%) and Versatis® (lidocaine medicated plaster 5%).

NCT ID: NCT04319926 Completed - Healthy Clinical Trials

Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Generic Lidocaine Patch 5% in Healthy, Adult, Human Subjects

Start date: September 7, 2018
Phase: Phase 1
Study type: Interventional

An open label, randomized, two-treatment, two-period, single-dose study evaluating the product adhesion in healthy, adult subjects using ZTlido 1.8% Topical System and a generic Lidocaine Patch 5%

NCT ID: NCT04312750 Completed - Healthy Clinical Trials

Adhesion of Lidocaine Topical System 1.8%

Start date: December 2015
Phase: Phase 1
Study type: Interventional

The objective of this study is to evaluate the adhesion performance of ZTlido (lidocaine topical system) 1.8% in normal, healthy volunteers.

NCT ID: NCT04250467 Completed - Clinical trials for Adhesion; Peritoneum

A Randomized Double-Blind Controlled Study of Alanyl-Glutamine for Adhesion Reduction

Start date: February 15, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

This study evaluates whether L-Alanyl-L-Glutamine can reduce the incidence, extent and severity of adhesions after myomectomy. Half of the participants will receive L-Alanyl-L-Glutamine and the other half of participants will receive a saline placebo at the time of myomectomy.

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: NCT04150536 Completed - Healthy Clinical Trials

Pharmacokinetics and Adhesion of Lidocaine Topical System 1.8% Under Conditions of Heat and Exercise

Start date: January 8, 2016
Phase: Phase 1
Study type: Interventional

The objectives of this study are to evaluate the pharmacokinetic and adhesion performance of ZTlido (lidocaine topical system) 1.8% during physical exercise, application of heat, and under normal conditions.