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Rupture clinical trials

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NCT ID: NCT01637610 Terminated - Clinical trials for Preterm Premature Rupture of Fetal Membranes

Detection of PPROM With AmniSure PAMG-1 Rapid Immunoassay

Start date: September 2011
Phase: N/A
Study type: Observational

The investigators will test the hypothesis that in a preterm population with a gestational age of 16+0 and 36+6 weeks AmniSure PAMG-1 rapid immunoassay will be more accurate than conventional methods (speculum examination for combination of pooling, nitrazine and ferning) for the detection of Preterm Prelabour Rupture of Membranes (PROM).

NCT ID: NCT01633294 Completed - Chorioamnionitis Clinical Trials

Antibiotic Prophylaxis in Prelabor Rupture of Membranes at Term

Start date: October 2008
Phase: Phase 2/Phase 3
Study type: Interventional

The aims of this study are to determine whether antibiotics administered routinely in women presenting with premature rupture of membranes later than the 37+0 weeks of gestation can alter the rate of maternal and neonatal infection and to compare these rates between prompt (< 12 hour) and delayed (≥ 12 hour) induction in the group of patients not submitted to antibiotic prophylaxis.

NCT ID: NCT01632774 Completed - Aortic Rupture Clinical Trials

Analysis of Risk Factors for Death After Blunt Traumatic Rupture of the Thoracic Aorta

Start date: January 1990
Phase: N/A
Study type: Observational

Aortic injuries after blunt thoracic trauma are compared to the great incidence of accidents relatively rare, but potentially serious leading to death at scene in most of the cases. The study was undertaken to delineate mortality and its risk factors on three different levels (pre-hospital, in-hospital and overall). Between 1990 and 2003, all consecutive patients and victims with traumatic aortic rupture were retrospectively analyzed by reviewing hospital and autopsy records.

NCT ID: NCT01622179 Unknown status - Clinical trials for Achilles Tendon Rupture

Outcome of Two Different Suture Methods for Achilles Tendon Rupture

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

The purpose of this study is to estimate the effective of two suture methods in the treatment of Achilles rupture.

NCT ID: NCT01616823 Completed - HIV Clinical Trials

Fetal HIV Transmission Risk and Duration of Membrane Rupture

Start date: January 2009
Phase:
Study type: Observational

In optimally managed HIV+ women with undetectable viral loads, who are on HAART and also receiving intrapartum IV ZDV, the risk of vertical transmission of HIV is independent of the length of time of rupture of membranes.

NCT ID: NCT01584323 Recruiting - Clinical trials for Preterm Premature Rupture of Membranes

Pomegranate to Reduce Maternal and Fetal Oxidative Stress and Improve Outcome in Pregnancies Complicated With Preterm Premature Rupture of the Membranes

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

In this study the investigators sought to determine the effects of Pomegranate (Natural pomegranate polyphenol (P. granatum L) extract) : 1. On the maternal and fetal oxidative stress and inflammation associated with PPROM. 2. On the time interval from PPROM to delivery and on fetal Ph and apger score.

NCT ID: NCT01544387 Completed - Pregnancy Clinical Trials

Preterm Premature Rupture of Membranes (PPROM): Bed Rest Versus Activity Trial

BRAT
Start date: July 2010
Phase: N/A
Study type: Interventional

The objective of this study is to determine, through a randomized clinical trial, whether bed rest is helpful for the management of pregnancies complicated by preterm premature rupture of membranes (PPROM).

NCT ID: NCT01538030 Completed - Premature Rupture Clinical Trials

Perinatal Outcome After Premature Rupture of Membranes

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

Premature rupture of membranes is an important cause of neonatal morbidity and mortality, mainly because of the complications associated with this pathology (oligohydramnios, cord compression or prolapse, infection). When rupture of the membranes occur the risk of cord compression increases but there is little evidence regarding this complication and amniotic fluid volume. The investigator's focus are the perinatal outcomes according to amniotic fluid volume (< 5 or >5).

NCT ID: NCT01503606 Completed - Clinical trials for Preterm Premature Rupture of Membrane

Duration of Antibiotics Treatment With Cefazolin and Clarithromycin in Women With Preterm Premature Rupture of Membrane

Start date: October 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the neonatal outcome and infant neurologic outcome whose mother were treated with cefazolin plus clarithromycin for one week or until delivery after preterm premature rupture of membrane.

NCT ID: NCT01470833 Completed - Clinical trials for Acute Achilles Tendon Rupture

Non-operative Treatment of Acute Achilles Tendon Rupture Using Dynamic Rehabilitation. Influence of Early Weight-bearing Compared With Non-weight-bearing

Start date: April 2011
Phase: N/A
Study type: Interventional

Acute achilles tendon rupture is relatively frequent (11 to 37 per 100,000). There are great social benefits in optimizing treatment and shortening recovery. There is no consensus concerning the best treatment of acute achilles tendon rupture. Traditionally, surgical treatment is considered superior, but more recent studies show evidence that non-operative treatment with early dynamic rehabilitation gives the same functional outcome with fewer side effects. Traditionally non-operative treatment involves non-weightbearing for 6 weeks. This is not evidence based rather due to tradition. It is well documented that mechanical load improves tendon healing in general and has no detrimental effect on the healing of operated achilles tendons. The objective of this randomized study is to compare early weight-bearing with non-weight-bearing following non-operative treatment of acutely ruptured Achilles tendons.