This trial was last updated 4 days ago.
Conditions bone mineral density, vascular malformations
Sponsor Mayo Clinic
Start date September 2015
End date October 2017
Trial size 15 participants
Trial identifier NCT02561182, 15-002284


The goal of this study is to determine whether or not patients with overgrowth syndromes have decreased bone density.

Recruiting in the following locations…

United States Minnesota
Other Countries No locations recruiting

Study Design

Observational model cohort
Time perspective prospective

Primary Outcomes

Evidence of decreased bone density in patients with vascular malformations, confirmed by DEXA scans
time frame: One year
Evidence of decreased bone density in patients with vascular malformations, confirmed by serum specific bone markers
time frame: One year

Eligibility Criteria

Male or female participants at least 5 years old.

Inclusion Criteria: - Age > 5 years such that the patient is able to cooperate with the DXA scan or Xtreme CT - Known clinical diagnosis of an overgrowth syndrome such as Klippel-Trenaunay Syndrome, CLOVE syndrome, Proteus syndrome, diffuse capillary malformation with overgrowth, or other unspecified OGS. Exclusion Criteria: - Age < 5 years - Inability to comply with the scan - No or uncertain diagnosis of an OGS. - Prior bisphosphonate use - Systemic steroids in the past 6 months - Pregnant women

Additional Information

Official title Bone Health in Patients With Overgrowth
Principal investigator Megha M Tollefson, MD
Description It is known that patients with complex vascular malformation are at risk of decreased bone density and even vanishing bone disease. However, what is not known is if patients with OGS are at decreased bone density at locations that are distant from the vascular malformation. This study will look at bone health in patient's with OGS in a cross sectional fashion. If they are found to be at a particular risk for decreased bone density then this can be addressed in early childhood, through nutrition and activity recommendations. The study will consist of 15 participants, all who have a known clinical diagnosis of an overgrowth syndrome, and will be >5 years old so that they can co operate with a DEXA or Xtreme CT scan. Study specifics: - They will be asked specific questions regarding medical and family history and an intake form will be filled out. - The height, weight, body mass index and Tanner stage measurements will be recorded during this visit. - Photos of the affected area(s) will be taken, however, this is optional. - A urine pregnancy test will be done in all females of childbearing potential . - Laboratory studies will be performed in all patients. - A 24-hour urine sample will be collected from adults who are able and willing; in children and in those not able or unwilling to provide a 24-hour urine, a spot urine will be collected. - Bone age will be assessed via plain film of the wrist - Bone density will be assessed for each patient via DEXA scan - Cortical and trabecular parameters and bone strength will be assessed by HRpQCT
Trial information was received from ClinicalTrials.gov and was last updated in October 2016.
Information provided to ClinicalTrials.gov by Mayo Clinic.