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Adhesion clinical trials

View clinical trials related to Adhesion.

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NCT ID: NCT05999162 Completed - Colorectal Cancer Clinical Trials

Mechanical Ileus in the Era of Minimally Invasive Colorectal Surgery

Start date: August 4, 2023
Phase:
Study type: Observational

The present study was to investigate if the incidence, patterns and surgical outcomes of mechanical ileus have changed in the era of minimally invasive surgery (MIS).

NCT ID: NCT05036525 Completed - Thyroid Diseases Clinical Trials

Evaluation of the Efficacy and Safety of a Hyaluronic Acid Gel in Adhesion Prevention After Open Thyroidectomy.

Start date: June 17, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to assess the safety and efficacy of HANBIO BarriGel to prevent thyroidectomy postoperative adhesions

NCT ID: NCT04837469 Completed - Adhesion Clinical Trials

Randomized Clinical Trial of Fissure Sealants Comparing Universal Adhesive With Etch-And-Rinse Adhesive After 24 Month

Start date: January 1, 2014
Phase: N/A
Study type: Interventional

Objective: This randomized, controlled clinical study aimed to evaluate the performance of one universal adhesive applied with etch-and-rinse or self-etch strategy and one etch-and-rinse adhesive on fissure sealant retention over 24 months. Methodology: 144 sealants were placed on the permanent premolars and molars of 13 subjects. Teeth were divided into three groups SB2(control): Adper Single Bond 2, SBU-ER: Single Bond Universal/etch-and-rinse, SBU-SE: Single Bond Universal/self-etch. After the adhesive application, Fissurit FX was applied and light-cured. Clinical evaluations were done at baseline and at 1 week, 6-, 12-, 18- and 24-month recalls. Visual examination was performed on every visit for evaluation of the sealants. Evaluating criteria were: 1= completely retained; 2= partial loss; 3= total loss. The Pearson Chi-square test was used for each evaluation period.

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: 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: 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.