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Tissue Adhesion, Surgery-Induced clinical trials

View clinical trials related to Tissue Adhesion, Surgery-Induced.

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NCT ID: NCT05058027 Completed - Clinical trials for Tissue Adhesion, Surgery-Induced

Anti-adhesive Effect and Safety of MEDICURTAIN Applied to Undergoing Thyroid Surgery (Pivotal Study)

Start date: July 4, 2013
Phase: N/A
Study type: Interventional

This study was designed to demonstrate the non-inferiority of MEDICURTAIN® (investigational device) compared to commercially available GUARDIX-SG® (control device) in treatment of subject who underwent total thyroidectomy for prevention of adhesion formation at 6 weeks after the surgery.

NCT ID: NCT05049434 Completed - Sinusitis Clinical Trials

Efficacy and Safety for Medicurtain® in Prevention of Adhesion After Endoscopic Sinus Surgery (Pivotal Study)

Start date: March 3, 2014
Phase: N/A
Study type: Interventional

This clinical trial is to prove that the treatment group of Medicurtain® is non-inferior to the treatment group of Guardix-sol®, test equipment on adhesion after endoscopic sinus surgery, upon the aspects of adhesion prevention efficacy and safety.

NCT ID: NCT04688281 Completed - Clinical trials for Tissue Adhesion, Surgery-Induced

Spine Surgery for Adhesions in Patients Evaluated for Efficacy and Safety of MedicurtainⓇ (Pivotal Study)

Start date: October 11, 2011
Phase: N/A
Study type: Interventional

This study was designed to evaluate the efficacy and safety of Medicurtain®, an antiadhesion barrier in patients who underwent In Situ Decompression for single level and unilateral herniated lumbar intervertebral disc. Subjects were randomly assigned either into Medicurtain® treatment group or control group. Adhesion formations between the two groups at 12 weeks after surgery were compared by using MRI-applied scar score, ODI (Oswestry Disability Index) and VAS.

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: 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.