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Craniosynostoses clinical trials

View clinical trials related to Craniosynostoses.

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NCT ID: NCT01094977 Suspended - Craniosynostoses Clinical Trials

Blood Loss and Transfusion Requirement in Infants Treated With Tranexamic Acid

Start date: January 2010
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to investigate whether tranexamic acid (TXA) reduces perioperative blood loss and transfusion requirement in infants undergoing craniosynostosis surgery.

NCT ID: NCT01006148 Withdrawn - Clinical trials for Metopic Craniosynostosis

Comparison of a Bone Product to Bone Dust in Ossification of Small Calvarial Defects.

DBM
Start date: October 2009
Phase: Phase 4
Study type: Interventional

In this study we want to compare the effectiveness of a bone substitute (Allogenix Plus, a product derived from a dead human being that has chosen to donate it prior to dying) and bone dust from the patient's own bone pieces, versus bone dust alone in filling in the gaps that sometimes occur after surgery for craniosynostosis . We will compare the percent of defect filled at 1 year in 5 patients 18 months or older with metopic craniosynostosis that received the bone substitute plus their bone dust with 5 previously operated patients with similar characteristics that received bone dust alone to fill in the gaps. The bone substitute that we are using will be provided at no cost by the company Biomet Microfixation. The bone substitute Allogenix Plus undergoes extensive screening for infectious diseases as well as processing to prevent a rejection. The product will be applied during standard surgery to 5 patients with metopic craniosynostosis of 18 months or older with skull defects no larger than 25 cm2, so it does not require any additional surgeries. Aside from the placement of this bone substitute the patient will proceed to receive the standard of care which includes a pre-operative CT scan, immediate post-operative CT scan, and 1 year post-operative CT scan of the Head. We will review these scans and look at percent of bony growth in the bone substitute plus bone dust group . We will also see the patients in clinic, during standard of care follow-up visits at 1 week, 3 weeks, 6 weeks, 12 weeks, 6 months, and 1 year post-operatively. During clinic visits we will monitor the patient closely for any potential side effects of the bone substitute as well as complications of the surgery. We will then review the charts of 5 patients 18 months or older that have undergone surgery for metopic craniosynostosis until 5 patients with similar characteristics and defect size have been obtained. We will compare their post-operative CT scans and pictures and we will look at bone growth, bone resorption, bone gaps present, and need for secondary surgeries.

NCT ID: NCT00912119 Completed - Craniosynostosis Clinical Trials

Amicar Pharmacokinetics of Children Having Craniofacial Surgery

Start date: May 2009
Phase: Phase 1
Study type: Interventional

Craniofacial reconstruction surgery involves a surgical approach to the craniofacial region to repair cranial vault and facial deformities. The surgery is extensive, often requiring wide scalp dissections and multiple osteotomies and has been associated with significant morbidity. Some of the most severe and commonly seen problems are associated with the rate and extent of blood loss. Efforts to minimize surgical bleeding may translate to reduced transfusion requirements and a lessening of associated risks Epsilon-aminocaproic acid (EACA), an inhibitor of fibrinolysis, reduces transfusion requirements in children undergoing procedures on cardiopulmonary bypass (CPB), as well as in older children undergoing spinal surgery for scoliosis (1-6). Before controlled studies to assess efficacy of EACA in a craniofacial surgical population can be done, appropriate pharmacokinetic (PK) data are needed to determine the optimal dosing strategy. PK data exist for EACA in children undergoing operations on CPB and hypothermia. The aim of this study is to determine the pharmacokinetics of EACA in infants and children undergoing craniofacial reconstruction procedures.

NCT ID: NCT00773643 Completed - Craniosynostosis Clinical Trials

Osteogenic Profiling of Tissue From Children With Craniosynostosis

Start date: April 2008
Phase: N/A
Study type: Interventional

The primary objectives of this study are - to procure human temporalis muscle, subcutaneous adipose (fat), and bone tissue samples from children with craniosynostosis, - to grow cells from these tissues in vitro, - to evaluate the osteogenic potentials of these cell types.

NCT ID: NCT00769847 Withdrawn - Craniosynostosis Clinical Trials

Endoscopic Treatment for Isolated, Single Suture Craniosynostosis

Start date: September 2008
Phase: N/A
Study type: Observational

This is a prospective study to evaluate outcomes in patients undergoing endoscopic craniectomy for isolated, single-suture craniosynostosis.

NCT ID: NCT00722436 Terminated - Bleeding Clinical Trials

Tranexamic Acid for Craniofacial Surgery

Start date: July 2008
Phase: Phase 4
Study type: Interventional

This is a randomized, blinded, prospective study that will investigate the potential benefit of tranexamic acid to reduce the intraoperative bleeding and blood transfusions in pediatric patients undergoing craniofacial surgeries.

NCT ID: NCT00579709 Completed - DiGeorge Syndrome Clinical Trials

Thymus Transplantation With Immunosuppression

884
Start date: July 2002
Phase: Phase 1
Study type: Interventional

The research purpose is to determine if thymus transplantation with immunosuppression is a safe and effective treatment for complete DiGeorge anomaly. The research includes studies to evaluate whether thymus transplantation results in complete DiGeorge anomaly subjects developing a normal immune system.

NCT ID: NCT00579527 Completed - Clinical trials for Complete DiGeorge Syndrome

Phase I/II Thymus Transplantation With Immunosuppression #950

#950
Start date: December 19, 2005
Phase: Phase 1/Phase 2
Study type: Interventional

The study purpose is to determine if cultured thymus tissue implantation (CTTI) (previously described as transplantation) with tailored immunosuppression based on the recipient's pre-implantation T cell population is a safe and effective treatment for complete DiGeorge anomaly. This study will also evaluate whether cultured thymus tissue implantation and parathyroid transplantation with immunosuppression is a safe and effective treatment for complete DiGeorge anomaly and hypoparathyroidism.

NCT ID: NCT00576836 Completed - DiGeorge Syndrome Clinical Trials

Thymus Transplantation Dose in DiGeorge #932

Start date: September 2, 2004
Phase: Phase 2
Study type: Interventional

One purpose of this study is to determine whether the amount of cultured thymus tissue implanted into DiGeorge anomaly infants has any effect on the immune outcome. Another purpose of this study is to determine whether parental parathyroid transplantation (in addition to cultured thymus tissue implantation (CTTI) can help both the immune and the calcium problems in DiGeorge infants with hypocalcemia. [Funding Source - FDA Office of Orphan Products Development (OOPD)]

NCT ID: NCT00576407 Completed - DiGeorge Syndrome Clinical Trials

Thymus Transplantation in DiGeorge Syndrome #668

Start date: October 1991
Phase: Phase 2
Study type: Interventional

The study purpose is to determine whether cultured thymus tissue implantation (CTTI) is effective in treating typical complete DiGeorge syndrome.