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Rupture clinical trials

View clinical trials related to Rupture.

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NCT ID: NCT03740022 Recruiting - Clinical trials for Anterior Cruciate Ligament Injury

ACL Versus ALL + ACL Study

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

The aim of the study is to show a reduction of a re-rupture rate with an ACL (antero crusader ligament) + ALL (anterolateral ligament) combined technique compared to a classical Kenneth-Jones ACL (antero crusader ligament) reconstruction technique.

NCT ID: NCT03717571 Completed - Clinical trials for Rotator Cuff Tear or Rupture, Not Specified as Traumatic

Superior Glenohumeral Translation in Patients With Degenerative Rotator Cuff Tears

ROTCUFF
Start date: October 4, 2018
Phase:
Study type: Observational

Degenerative partial and complete rupture of the rotator cuff is a common injury among elder patients. However, the clinical manifestation varies largely with some patients having severe pain and limiting range of motion and others having no complaints. The basic functions of the rotator cuff are to facilitate shoulder motion and stabilization and centering of the glenohumeral joint. The objective of this study is to quantify the difference in superior glenohumeral translation in patients with degenerative rotator cuff tear compared to healthy control subjects and to determine the effect of isolated complete supraspinatus tear and combined complete supraspinatus and either partial infraspinatus or partial subscapularis tear.

NCT ID: NCT03715530 Terminated - Preterm Birth Clinical Trials

Use of Placental Alpha Microglobulin-1(PAMG-1) to Diagnose Premature Rupture of Membranes in Pregnant Women

PAMG-1
Start date: September 2007
Phase: N/A
Study type: Interventional

The study is to evaluate the accuracy of a test device called "PAMG-1" to see if a pregnant women has ruptured membranes in comparison to standardly used testing methods.

NCT ID: NCT03711734 Completed - Anesthesia Clinical Trials

Acupuncture ACL (Anterior Cruciate Ligament)

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

Acupuncture research in regards to PONV has been fairly well established, however, studies about perioperative pain control and acupuncture are a little more murky. In 2008, a meta analysis looked at randomized controlled studies and found that while acupuncture was shown to decrease pain, there were limitations including credible placebo or sham intervention, and thus, blinding. The main purpose of this feasibility trial is to determine whether or not adequate blinding is possible in the intraoperative setting with the patient sedated.

NCT ID: NCT03704532 Active, not recruiting - Clinical trials for Achilles Tendon Rupture

Nonoperative Treatment of Acute Achilles Tendor Rupture

NoArc
Start date: April 1, 2017
Phase:
Study type: Observational

A prospective, non-randomised, observational study to investigate the clinical and biomechanical outcomes and prevalence of reruptures after operative or nonoperative treatment of acute achilles tendon rupture.

NCT ID: NCT03689062 Not yet recruiting - Clinical trials for Premature Rupture of Membrane

Premature Rupture of Membranes at 34 to 37 Weeks' Gestation

Start date: May 2019
Phase: N/A
Study type: Interventional

Prelabour rupture of membrane is deļ¬ned as rupture of membranes prior to the onset of labour. Approximately 8% of pregnant women at term experience PROM, but the decision as to how term PROM should be managed clinically remains controversial, and there is wide variation in practice with no clear consensus on what constitutes optimal treatment. Although for the majority of women labour will start spontaneously within 24 hours following term PROM, up to 4%of women will not experience spontaneous onset of labour within seven days.

NCT ID: NCT03681899 Completed - Clinical trials for Geriatric Assessment

Evaluation of Rupture of Galenic Practices at Home in a Population Aged 65 or Older

CRUSHAGE
Start date: September 18, 2018
Phase:
Study type: Observational

Elderly people frequently take several medications and are exposed to iatrogenic risks. The oral route is the preferred route of administration. The effectiveness and the safety of the drugs depend in particular on the modes of administration (frequency of the intake, respect of the doses and the galenic ...). However, these modalities are very little known concerning the treatments intake at home in the elderly population. In a health facility welcoming geriatric patients, the rupture of galenic is frequent and favored by swallowing disorders, dependence, the increase in age, the presence of cognitive disorders or psycho-behavioral disorders. The consequences of the rupture of galenic are numerous, concern the patients but also the caregivers who administer the treatments.

NCT ID: NCT03680716 Completed - Postoperative Pain Clinical Trials

Combined Saphenous Nerve and IPACK Blocks Versus Infiltration Analgesia After Anterior Cruciate Ligament Reconstruction

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

A lot of patient have posterior knee pain after ACL reconstruction despite saphenous nerve block. Recently a new block has been described, know as IPACK block (interspace between the popliteal artery and the capsule of the posterior knee). The objective of this randomized controlled double-blinded trial is to assess whether a combined saphenous nerve block with IPACK block is more effective for the postoperative pain than a local infiltration analgesia.

NCT ID: NCT03671421 Active, not recruiting - Clinical trials for Anterior Cruciate Ligament Rupture

Number One Overall Graft Pick? Hamstring vs Bone-Patellar-Tendon-Bone vs Quadriceps Tendon

Start date: September 11, 2018
Phase: N/A
Study type: Interventional

The main purpose of this study is to determine if there is a difference in graft re-injury/failure rates between participants that have had an ACL reconstruction with a STG, BPTB or QT autograft. Additionally, to compare quality of life, patient reported outcomes and functional performance after ACL reconstruction with STG, BPTB and QT.

NCT ID: NCT03670550 Withdrawn - ACL Injury Clinical Trials

Dynamic ACL Brace: In Vivo Kinematics

Start date: October 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of the Össur Rebound dynamic ACL brace on knee kinematics evaluated using dynamic stereo X-ray (DSX) imaging during functional activities. Brace performance will be evaluated before and after ACL reconstruction.