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Rupture clinical trials

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NCT ID: NCT01891006 Completed - Clinical trials for Surgical Wound Infection

Intervention for Postpartum Infections Following Caesarean Section

APIPICS
Start date: May 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether Negative Pressure Wound Therapy is an effective wound treatment compared to conventional wound treatment in the period of time from reoperation to re-suturing in women having surgical wound rupture after Caesarean Section.

NCT ID: NCT01890720 Completed - Clinical trials for Surgical Wound Infection

Incisional Negative Pressure Wound Therapy for Prevention of Postoperative Infections Following Caesarean Section

Start date: September 10, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether obese women (BMI >= 30) who give birth by caesarean section have a reduced incidence of wound infection and dehiscence when incisional Negative Pressure Wound Therapy is applied prophylactically following caesarean section.

NCT ID: NCT01833936 Completed - Clinical trials for Achilles Tendon Rupture

E-Stim and Achilles Tendon Repair Study

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

Calf muscle atrophy (muscle degeneration) is common following Achilles tendon repair due to the immobilization period necessary to ensure optimal healing. The purpose of this study is to determine if the use of neuromuscular electrical stimulation (NMES) after Achilles tendon surgery will reduce calf muscle atrophy.

NCT ID: NCT01785264 Completed - Clinical trials for Rupture of Achilles Tendon

Treatment Results After Acute Rupture of the Achilles Tendon.

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

To compare the end-results of three different methods of treatment of acute achilles tendon ruptures, it is necessary to establish identical rehabilitation protocols. Traditionally, early mobilization has been reserved for patients treated surgically and this may have unintentionally skewed treatment results. The investigators have therefore designed a prospective randomized trial performed as collaboration between Akershus University Hospital (Ahus), Oslo University Hospital (The Emergency Department), Østfold Hospital (Fredrikstad) and Drammen Hospital. The four institutions were chosen because of their geographical proximity and because they jointly have a substantial catchment area. Treatment is divided into three arms, and patients between 18 and 60 years of age sustaining first time achilles tendon ruptures will be invited to participate.

NCT ID: NCT01778816 Completed - Clinical trials for Achilles Tendon Ruptures

Calf Muscle Atrophy After Achilles Tendon Rupture. A Clinical-Radiological-Biomechanical Multicenter Study.

Start date: January 2009
Phase: N/A
Study type: Observational

Multicenter Achilles tendon study Switzerland. Comparing three mainstream treatment types: open, percutaneous and conservative (non-operative) treatments. Comparing force torque measurements, muscle volume and clinical scores.

NCT ID: NCT01775046 Completed - Aortic Diseases Clinical Trials

Valiant Thoracic Stent Graft With the Captivia Delivery System in the Treatment of Descending Thoracic Aortic Diseases (VALIANT CAPTIVIA France)

Start date: March 23, 2013
Phase:
Study type: Observational

The objective of this study is to assess the benefits of endovascular technique in terms of efficacy and safety of Valiant Thoracic Stent Graft with the Captivia Delivery System in the treatment of thoracic aortic disease, in a cohort of patients representative of the population treated under real-life conditions of use in France for up to 5 years.

NCT ID: NCT01762371 Completed - Clinical trials for Totally Ruptured Anterior Cruciate Ligament in the Knee

Khalifa Acute Effects

Start date: December 2012
Phase: N/A
Study type: Interventional

The primary hypothesis is that Khalifa's therapy has different acute effects in various organ systems i.e. proprioceptive, neuro-muscular, endogenous dopamine system, etc. These effects might indicate the pathway of the therapy.

NCT ID: NCT01752088 Completed - Clinical trials for Rupture Subscapularis Tendon

Repair of Subscapularis Tear :Clinical Results and MRI Analysis

Start date: June 1, 2012
Phase:
Study type: Observational [Patient Registry]

This study is to evaluate the magnetic resonance imaging (MRI) and clinical results of arthroscopic repair of subscapularis tears

NCT ID: NCT01736852 Completed - Clinical trials for Premature Rupture of Fetal Membranes

Evaluation of CRB in PROM Patients

Start date: November 2012
Phase: N/A
Study type: Interventional

The CRB study is designed to study the safety and effectiveness of the Cook Cervical Ripening Balloon (CRB) for the induction of labor in term and near-term patients with premature rupture of membranes (PROM).

NCT ID: NCT01698827 Completed - Clinical trials for Gastrostomy Tube Durability

Replacement Gastrostomy Tubes: Technical and Clinical Comparison of Five Commercial Models

Start date: January 2012
Phase: N/A
Study type: Observational

Multiple models of replacement tubes for percutaneous endoscopic gastrostomy are available in the market, however durability is variable. In a prospective randomized study, five commercial devices available in the market will be tested in 20 consecutive patients each. Tube performance will be observed during 6 months and durability will be assessed by Kaplan-Meier curves as well as Cox regression analysis.It is hypothesized that tube design and material will influence outcome.