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Clinical Trial Details — Status: Recruiting

Administrative 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

Study information

Verified date December 2023
Source Boston Children's Hospital
Contact Kelsey Deemer, BS
Phone 617-355-5226
Email Lymphaticregistry@childrens.harvard.edu
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


Description:

The purpose of the Lymphatic Anomalies Registry, created at Boston Children's Hospital, is to create a database to help current and future patients diagnosed with a lymphatic anomaly. The ultimate goal of the registry is to better understand and predict responses to therapies and risk factors for complications. Although the Lymphatic Anomalies Registry exists at Boston Children's Hospital, patients can be entered into the registry regardless of whether or not they visit Boston Children's Hospital, thus increasing the program's accessibility. The Lymphatic Anomalies Registry includes patients who have vascular anomalies with a lymphatic component across various diagnoses. From the patient's perspective, participation in the Lymphatic Anomalies Registry means taking part in a short, thirty minute interview, and providing the registry with access to medical records. The interview is conducted verbally with study staff of the Lymphatic Anomalies Registry, and can take place either at the hospital, or over the phone. During the interview, the registry will inquire about the patient's diagnosis, disease features, medical therapies, and procedures. Interested prospective patients will receive an introductory packet from the registry with information on how to proceed in the registry process. All obtained patient information is housed on a secure, HIPPA compliant, internal database, managed by Boston Children's Hospital staff. Patient information entered into the external database is de-identified. The research teams will also obtain a medical record release form to request the patient's medical record for review in our study.


Recruitment information / eligibility

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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Boston Children's Hospital Boston Massachusetts

Sponsors (2)

Lead Sponsor Collaborator
Boston Children's Hospital Lymphatic Malformation Institute

Country where clinical trial is conducted

United States, 

References & Publications (3)

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

Outcome

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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