Lymphatic Malformation Clinical Trial
Official title:
Lymphatic Anomalies Registry for the Assessment of Outcome Data
NCT number | NCT02399527 |
Other study ID # | P00007182 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | June 2013 |
Est. completion date | June 2035 |
Lymphatic anomalies are a rare subset of vascular anomalies that are poorly understood. the understanding of the natural history, long-term outcomes, risk factors for morbidity and mortality, and the relative benefit of medical therapies and procedures is limited.The goal of this project is to better understand these diseases and improve the care of theses rare patients. To do this, the investigators are conducting an observational study of patients with lymphatic anomalies, including an annual follow-up questionnaire to gather prospective data on mortality, morbidity, treatments, and functionality as well as quality of life.
Status | Recruiting |
Enrollment | 1000 |
Est. completion date | June 2035 |
Est. primary completion date | June 2035 |
Accepts healthy volunteers | No |
Gender | All |
Age group | N/A and older |
Eligibility | Inclusion Criteria: - Clinical diagnosis of complex vascular tumor, malformation or overgrowth syndrome with significant lymphatic component |
Country | Name | City | State |
---|---|---|---|
United States | Boston Children's Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston Children's Hospital | Lymphatic Malformation Institute |
United States,
Croteau SE, Kozakewich HP, Perez-Atayde AR, Fishman SJ, Alomari AI, Chaudry G, Mulliken JB, Trenor CC 3rd. Kaposiform lymphangiomatosis: a distinct aggressive lymphatic anomaly. J Pediatr. 2014 Feb;164(2):383-8. doi: 10.1016/j.jpeds.2013.10.013. Epub 2013 — View Citation
Rankin H, Zwicker K, Trenor CC 3rd. Caution is recommended prior to sildenafil use in vascular anomalies. Pediatr Blood Cancer. 2015 Nov;62(11):2015-7. doi: 10.1002/pbc.25600. Epub 2015 May 15. — View Citation
Strychowsky JE, Rahbar R, O'Hare MJ, Irace AL, Padua H, Trenor CC 3rd. Sirolimus as treatment for 19 patients with refractory cervicofacial lymphatic malformation. Laryngoscope. 2018 Jan;128(1):269-276. doi: 10.1002/lary.26780. Epub 2017 Aug 7. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To characterize the heterogeneity of lymphatic disorders, including demographics, presentation, and complications. | 15 years | ||
Primary | To identify factors that are prognostic of the occurrence of complications, including effusions, coagulopathy, ectatic draining veins, prior infections, visceral involvement, bone involvement, and development of cardiopulmonary symptoms. | 15 years | ||
Primary | To identify factors prognostic of poor outcome and use them to develop "staging" of lymphatic anomalies. | 15 years | ||
Primary | To describe the natural history of lymphatic anomalies, including morbidity and mortality. | 15 years | ||
Primary | To describe the therapies (medical and procedural), adverse events and responses to therapy in patients with lymphatic anomalies. | 15 years | ||
Primary | To pilot quality of life, functional assessment and pain scoring tools in this patient population. | 15 years | ||
Secondary | To estimate the proportion of time that patients with lymphatic anomalies have affected offspring. | 15 years | ||
Secondary | To assess for correlations of pregnancy complications or medications taken during pregnancy with the development of lymphatic anomalies. | 15 years |
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