Clinical Trials Logo

Tissue Adhesions clinical trials

View clinical trials related to Tissue Adhesions.

Filter by:

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: NCT04637373 Recruiting - Clinical trials for Intrauterine Adhesion

Hysteroscopy Assisted Suction Curettage for Early Pregnancy Loss

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

Retained products of conception (RPOC) and intrauterine adhesions (IUA) may occur following suction curettage for early miscarriage and cause secondary infertility, recurrent pregnancy loss and pregnancy complications. The aim of this study is to investigate whether adding hysteroscopy to suction curettage reduces the rates of RPOC and IUA.

NCT ID: NCT04548570 Recruiting - Clinical trials for Intraperitoneal Adhesions After Rectus Muscles Approximation

Closure vs Non Closure of Rectus Muscle at Cesarean Section 5 Year Study

Start date: January 1, 2020
Phase:
Study type: Observational

approximation of both recti during lower segment cesarean section may be an important step to lower incidence of intraabdominal adhesions . peritoneal adhesions are of major medical importance and are associated with clinical problems such as chronic pain and infertility.

NCT ID: NCT04483986 Active, not recruiting - Muscle Injury Clinical Trials

Does Rectus Re-approximation Cause Adhesion After Cesarean Section?

Start date: May 25, 2020
Phase: N/A
Study type: Interventional

Rectus re-approximation and periton closure are not the obligatory steps during cesarean section. These steps are due to surgeon's preference. However, there is lack of knowledge about the relation of rectus muscle re-approximation and adhesion formation. We are going to study the rectus muscle stiffness by share-wave elastosonography.

NCT ID: NCT04482140 Not yet recruiting - Clinical trials for Tissue Adhesions, Surgery-Induced

Post Approval Study to Evaluate the Safety and Performance of GENTA-FOIL Resorb® in Hand Surgery

Start date: April 2024
Phase:
Study type: Observational

Single arm study to evaluate the safety and performance of Genta-Foil resorb® for the prevention of tissue adhesions

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.