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Rupture clinical trials

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NCT ID: NCT00463099 Completed - Clinical trials for Rupture of Anterior Cruciate Ligament

Multicenter Orthopaedics Outcomes Network for ACL Reconstructions

Start date: January 2002
Phase:
Study type: Observational

The purpose of this study is to determine the effect of modifiable risk factors on knee function, osteoarthritis, and re-rupture of the anterior cruciate ligament (ACL) following ACL reconstruction.

NCT ID: NCT00439907 Completed - Childbirth Clinical Trials

Comparison of Overlap and End-to-end Repair in Anal Sphincter Rupture During Delivery

Start date: February 2005
Phase: N/A
Study type: Interventional

Rupture of the external anal sphincter occurs in about 4% percent of deliveries. It is not clear from other studies whether the results concerning anal function, e.g. fecal continence, are better with the overlap repair or end-to-end repair of the injured muscle. The researchers randomize women at birth to either overlap or end-to-end when the injury is recognized, and examine them one year later with special anal physiologic examinations and a validated questionnaire. The hypothesis is that the overlap technique is superior.

NCT ID: NCT00435032 Completed - Clinical trials for Ruptured Appendicitis

Early Versus Interval Appendectomy for Ruptured Appendicitis in Children

RAPTOR
Start date: October 2006
Phase: Phase 3
Study type: Interventional

The purpose of this randomized trial is to compare two commonly utilized surgical treatments for children with ruptured appendicitis: early appendectomy, versus interval appendectomy. The primary outcome measure is time away from normal activities.

NCT ID: NCT00434837 Completed - Clinical trials for Anterior Cruciate Ligament Rupture

Initial Graft Tension and ACL Surgery

Start date: February 2004
Phase: N/A
Study type: Interventional

The anterior cruciate ligament (ACL) is one of four strong ligaments connecting the bones of the knee joint. If overstretched, the ACL can tear. Reconstruction of a torn ACL is now a common surgical procedure. The amount of tension applied to the ACL during reconstruction may indirectly affect the possible onset of arthritis over time. The purpose of this study is to determine the effect of initial graft tension set during ACL reconstruction surgery on the progression of knee arthritis over at least a 15-year period.

NCT ID: NCT00397735 Completed - Inflammation Clinical Trials

N-acetylcysteine in Intra-amniotic Infection/Inflammation

Start date: October 1, 2006
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of the study is to determine if N-acetylcysteine (a potent free radical scavenger) prevents the occurrence of adverse neonatal outcomes in preterm deliveries complicated by infection associated with preterm labor or preterm premature rupture of membranes (PPROM). The working hypothesis is that in pregnancies complicated by intra-amniotic infection or inflammation, N-acetylcysteine protects the fetus by preventing the development, or decreasing the intensity and/or progression of the fetal inflammatory syndrome.

NCT ID: NCT00355966 Completed - Clinical trials for Premature Rupture of Membranes at Term

Comparison of Misoprostol and PGE2 Gel for Induction of Labour in Women With Premature Rupture of Membranes at Term

Start date: August 2006
Phase: Phase 4
Study type: Interventional

Induction of labour with vaginal misoprostol, in women with premature rupture of membranes at term, results in significant shortening of induction to delivery time in comparison to vaginal PGE2 gel induction.

NCT ID: NCT00355303 Completed - Clinical trials for Premature Rupture of Membranes at Term

Comparison of Misoprostol and Prostaglandin E2 (PGE2) Gel for Induction of Labour in Premature Rupture of Membranes at Term

Start date: August 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether induction of labor with vaginal misoprostol application will result in fewer cesarean deliveries than vaginal PGE2 gel application in women with premature rupture of membranes at term.

NCT ID: NCT00342667 Completed - Pregnancy Clinical Trials

Clinical, Biochemical, Histological and Biophysical Parameters in the Prediction of Cerebral Palsy in Patients With Preterm Labor and Premature Rupture of Membranes

Start date: December 8, 1997
Phase:
Study type: Observational

A major goal of modern perinatal and neonatal medicine is to reduce the rate of developmental disabilities, especially mental retardation. Cerebral palsy is frequently associated with neurologic abnormalities and mental retardation. Improvements in neonatal intensive care have resulted in improved survival of very low birthweight infants but also in an increased frequency of cerebral palsy. Prematurity is a leading risk factor for cerebral palsy. Two thirds of preterm neonates are born to mothers with preterm labor with intact membranes or preterm premature rupture of membranes. A growing body of evidence suggests that these conditions are heterogeneous. This is an observational cohort study designed to identify the mechanisms of disease in patients with preterm labor/contractions and preterm premature rupture of membranes and to describe the relationship between clinical, biochemical, histological, biophysical parameters and the development of infant neurological disorders.

NCT ID: NCT00342277 Completed - Preterm Birth Clinical Trials

Microarray Expression Profiling to Identify Stereotypic mRNA Profiles in Human Parturition

Start date: December 21, 1999
Phase:
Study type: Observational

The understanding of the biological mechanisms underlying preterm birth is very limited, making prevention of preterm birth difficult. The incidence of preterm birth worldwide varies between 6%-11% in singleton pregnancies, and 64-93% of preterm deliveries occur after the spontaneous onset of labor (preterm labor). The risk factors associated with preterm birth include demographic variables such as ethnic group, past obstetric history, and complications of the current pregnancy such as infection and fetal congenital anomalies. The current study aims to investigate the basic mechanisms of preterm labor by systematically cataloging the changes in expression levels of all expressed genes whose sequences are available. The goals will be accomplished by using microarray technology followed by subsequent confirmative or complementary analyses.

NCT ID: NCT00284648 Completed - Clinical trials for Achilles Tendon Rupture

Operative Versus Non-operative Treatment of Achilles Tendon Rupture

Start date: December 2000
Phase: N/A
Study type: Interventional

This study is intended to determine whether the optimal treatment of acute Achilles tendon ruptures is surgical repair or functional bracing. Our hypotheses are surgical repair will: 1) Result in a clinically relevant decrease in re-rupture rate and 2) Result in a clinically relevant improvement in disease specific quality of life and 3) A clinically relevant improvement in functional outcome measures