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Rupture clinical trials

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NCT ID: NCT02754674 Completed - Clinical trials for Rupture of Anterior Cruciate Ligament

Comparison of Femoral Tunnel and Clinical Outcome Using Two Anterior Cruciate Ligament Reconstruction Techniques

Start date: May 2014
Phase: N/A
Study type: Interventional

1. Purpose :To compare of femoral tunnel placement, tunnel geometry and clinical outcome using two anterior cruciate ligament reconstruction techniques ; transportal technique with flexible reamer and single bundle outside in technique with remnant preservation. 2. Subjects: anterior cruciate ligament (ACL) injury 66 patients - Double bundle transportal technique with flexible reamer: 33 - Single bundle outside in technique with remnant preservation: 33

NCT ID: NCT02740452 Recruiting - Clinical trials for Anterior Cruciate Ligament Rupture

Anterior Cruciate Ligament Rupture

LIGAMYS
Start date: September 2016
Phase: N/A
Study type: Interventional

The assess results of Anterior Cruciate Ligament (ACL) repair with the Ligamys® surgical technique versus standard technique. The aim of the study is to compare (laxity, instability, and safety) these two types of treatment by using a prospective, randomised multicenter analysis.

NCT ID: NCT02724072 Completed - Aortic Aneurysm Clinical Trials

Thoraflex™ Hybrid IDE Study

Start date: August 22, 2016
Phase: N/A
Study type: Interventional

The study will assess the effectiveness, safety and clinical outcomes of the Thoraflex™ Hybrid Device in the treatment of aortic disease affecting the aortic arch and the descending thoracic aorta, with or without involvement of ascending aorta. The study will also assess safety and early clinical outcomes in patients who receive an extension procedure within 1 year of Thoraflex™ Hybrid Device implantation. Lastly the study will assess the safety and clinical outcomes of patients who receive a Thoraflex™ Hybrid Device for treatment of a ruptured aorta. Patients will be followed for 3 years. The Primary Endpoint will be freedom from defined Major Adverse Events (MAE) occurring ≤ 1 year post-procedure.

NCT ID: NCT02702297 Completed - Clinical trials for Preterm Premature Rupture of Membranes

Multimodal Monitoring of Fetal Risk of Inflammation in Preterm Premature Rupture of Membranes

MuMFI-PPROM
Start date: January 7, 2016
Phase:
Study type: Observational

The purpose of this study is to examine whether the value of vaginal fluid cytokine levels as well as computerized fetal ECG analysis are suitable clinical parameters to detect an imminent intra-amniotic inflammation with a high risk of fetal inflammatory response syndrome (FIRS) or a neonatal early onset sepsis (EOS) and whether these parameters can be determined on a daily basis in the clinical monitoring of pregnancies complicated by PPROM.

NCT ID: NCT02680821 Active, not recruiting - Clinical trials for Rupture of Anterior Cruciate Ligament

Reconstruction of the Anterolateral Ligament (ALL) With Revision Anterior Cruciate Ligament (ACL) Surgery

Start date: February 2016
Phase: N/A
Study type: Interventional

Patients with combined Anterolateral ligament (ALL) reconstruction- Anterior cruciate ligament (ACL) revision will have a better rotational knee stability and therefore better patient reported outcome measure (PROM) scores compared to patients, who have ACL revision surgery without ALL reconstruction.

NCT ID: NCT02677506 Completed - Clinical trials for Cubital Tunnel Syndrome

Infraclavicular or Supraclavicular Brachial Plexus Blocks for Elbow Surgery

Start date: January 2013
Phase: N/A
Study type: Interventional

This study compares the infraclavicular approach to supraclavicular approach of brachial plexus block for elbow surgery.

NCT ID: NCT02635451 Not yet recruiting - Clinical trials for Preterm Premature Rupture of Membranes

The Relation Between Serum Ascorbic Acid Concentration and Preterm Premature Rupture of Membranes

Start date: January 2016
Phase: N/A
Study type: Observational

To study the association between maternal serum vitamin C concentration in women with preterm premature rupture of membranes (PPROM) and women without PPROM.

NCT ID: NCT02598843 Completed - Clinical trials for Rupture of Achilles Tendon

Standard Non Operative Treatment Versus Accelerated Rehabilitation of Achilles Tendon Ruptures

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

The purpose of this study is to directly compare traditional plaster treatment with early weightbearing in a walking boot for the non operative treatment of acute achilles tendon rupture.

NCT ID: NCT02584452 Completed - Clinical trials for Rupture of Anterior Cruciate Ligament

Trial Evaluating Postop Pain and Muscle Strength Among Regional Anesthesia Techniques for Ambulatory ACL Reconstruction

Start date: November 3, 2015
Phase: N/A
Study type: Interventional

Despite the apparent multifaceted benefit in differentiating blockade sites and duration of nerve blockade, the efficacy of continuous adductor canal blockade utilized specifically in ACL reconstruction has not been extensively studied. This study will test the hypothesis that the use of the adductor canal continuous nerve catheter will result in lower subjective pain scores on postoperative day 2 and improved quadriceps strength on postoperative day 1.

NCT ID: NCT02548013 Recruiting - Clinical trials for Preterm Premature Rupture of Membranes

Preterm Premature Rupture of Membranes, Outpatient Management vs Inpatient Management

Start date: August 2014
Phase: N/A
Study type: Interventional

This study is to compare the maternal and neonatal outcomes in the patients with PPROM who are managed at home versus those managed at hospital, half the patients will be managed at home and the other half will be managed inpatient.