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Adhesion clinical trials

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NCT ID: NCT04475367 Not yet recruiting - Blood Pressure Clinical Trials

Evaluation of the Effect of an APP in Improving Treatment Adherence in Hypertensive Patients in Hypertension Ambulatory

Start date: July 10, 2020
Phase: N/A
Study type: Interventional

Brief Summary: Through the App, the user will have the opportunity to connect directly with the health professional, clarify doubts and manage the treatment of their hypertension.

NCT ID: NCT04271150 Active, not recruiting - Dental Caries Clinical Trials

Efficiency of Different Modes of Universal Adhesive

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

The purpose of this study is to evaluate and compare the clinical performance of a Universal adhesive's different application modes.

NCT ID: NCT04023383 Completed - Quality of Life Clinical Trials

New Cross Linked Hyaluronan Gel After Deep Infiltrating Endometriosis Surgery

HYALOENDOQoL
Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Hyaluronan, a glycosaminoglycan found in connective tissues and extracellular matrix, has been postulated to reduce postoperative adhesions, because of its unconditioned biological functions at tissue repair but unfortunately it has a fluid nature that causes rapid degradation, and it cannot effect long enough to work as an adhesion barrier.(10,11) For this reason a New cross-linked hyaluronan (NCH) gel, that has higher viscosity compared to natural hyaluronan has been developed by BioRegen Biomedical (Changzhou, Jiangsu, China). It has the ability for gradually absorption within 1 to 2 weeks in vivo, which are the acquired repair period and the critical time for adhesion formation. Although it seems evident that endometriosis has a serious impact on the daily Quality of Life of women; comparable data for the effect of adhesion barriers to patients who have had laparoscopic (Deep infiltrating endometriosis) DIE surgery is missing. Therefore a pilot randomised controlled study was conducted to evaluate the effect of NCH gel on short term quality of life in patients who had undergone laparoscopic surgery due to DIE.

NCT ID: NCT03880435 Active, not recruiting - Infertility Clinical Trials

HYALOBARRIER® GEL ENDO Versus no HYALOBARRIER® GEL ENDO Following Operative Hysteroscopy for Improving Reproductive Outcome in Women With Intrauterine Pathology Wishing to Become Pregnant

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

To compare the costs and effects of HYALOBARRIER® GEL ENDO versus no HYALOBARRIER® GEL ENDO for increasing the chance of conception leading to live birth measured at 30 weeks after randomization in women wishing to become pregnant after surgical removal of intrauterine pathology (endometrial polyps, fibroids with uterine cavity deformation, uterine septa, IUAs or RPOC after miscarriage) by hysteroscopy as an outpatient or in hospital treatment.

NCT ID: NCT03660787 Completed - Adhesion Clinical Trials

Efficacy and Dose Ranging Study of Seroguard

Start date: May 4, 2017
Phase: Phase 2
Study type: Interventional

This trial was a multi-center, double-blind, randomized, parallel group, placebo-controlled, phase II study in adult hospitalized female patients with the confirmed diagnosis of pelvic adhesive disease in Study centres in Russia.

NCT ID: NCT03640559 Completed - Adhesion Clinical Trials

Safety and Tolerability of Seroguard Use

Start date: May 19, 2015
Phase: Phase 1
Study type: Interventional

The performed study of safety and tolerability of Seroguard, solution (JSC Pharmasyntez, Russia) in patients, undergoing planned laparoscopic cholecystectomy, demonstrated that patients from the both groups had the similar safety profile

NCT ID: NCT03443583 Completed - Adhesion Clinical Trials

Immediate and Delayed Dentin Sealing Effect on Partial Crowns

Start date: November 1, 2013
Phase: N/A
Study type: Interventional

Immediate Dentin Sealing as an adjunct to adhesive cementation of all ceramic restorations is proposed and executed in several studies, but there is very limited evidence to support its effectiveness. It is presumed that IDS both reduces postoperative sensitivity and increases the bond strength to dentin as compared to DDS.

NCT ID: NCT03293186 Completed - Thyroidectomy Clinical Trials

Anti-adhesive Effect and Safety of "Thermo-sensitive Adhesion Barrier (MEDICLORE)"

Start date: July 1, 2017
Phase: Phase 4
Study type: Interventional

One of most important complication of thyroid surgery is adhesion. There are many anti-adhesive materials, but none of them showed significant outcomes. The investigators planned double blind prospective study of "Thermo-sensitive Adhesion Barrier (MEDICLORE)" to reveal anti-adhesive effect of MEDICLORE. The investigators will recruit total 90 patients (control group 45, experimental group 45) and compare postoperative outcomes about adhesion.

NCT ID: NCT02434601 Active, not recruiting - Adhesion Clinical Trials

Dentin Treatments for Restorations of Cervical Lesions Non-Carious

Start date: March 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The surface of non-carious cervical lesions (LCNC) is a challenge to adhesive systems, it presents a dentin layer sclera hypermineralized, presence of bacteria and lack of mechanical retention, so this study aimed to evaluate the influence of different surface treatments on LCNC through a randomized clinical trial. Patients with LCNC were referred to the study and selected according to the inclusion criteria, such as the presence of at least 3 LCNC. Three different types of surface treatment were carried out in LCNC: control group, 15 seconds of etching dentin; Group I, acid etching of dentin in 30 seconds; and group II, cavity prophylaxis with ultrasound for 30 seconds. The remaining steps of the adhesive and restorative procedure was the same for all groups, following the material manufacturer's recommendations. Evaluations of restorations will be carried out in periods of one week (baseline), six months, one year, two years and three years as of tooth sensitivity, integrity and color change. Data will be analyzed by McNemar and chi-square test.