Status:
COMPLETED
Alendronate Osteoporosis Study
Lead Sponsor:
Boston Children's Hospital
Collaborating Sponsors:
Glaser Pediatric Research Network
Elizabeth Glaser Pediatric AIDS Foundation
Conditions:
Glucocorticoid-Associated Osteopenia and Osteoporosis
Eligibility:
All Genders
8-22 years
Phase:
PHASE2
PHASE3
Brief Summary
This trial will test the hypothesis that among 20 children and adolescents from Children's Hospital, Boston with Crohn's disease, ulcerative colitis, systemic-onset juvenile rheumatoid arthritis, juve...
Eligibility Criteria
Inclusion
- Subjects must be diagnosed with either ulcerative colitis, Crohn's disease, systemic-onset juvenile rheumatoid arthritis, juvenile dermatomyositis, systemic lupus erythematosus (SLE), mixed connective tissue disease (MCTD) or vasculitis according to standard criteria where available, and according to treating physicians when not available.
- Subjects must have diminished AP lumbar spine (L1-L4) BMD by DXA (Hologic 4500) with a Z score ≤ -1.5 SD assessed within 8 weeks of the Baseline Visit.
- Subjects must have received daily, alternate day or weekly systemic glucocorticoid therapy for a minimum of six months total in their life-time.
- Subjects must be between the ages of 8 and 21 years, 11 months, at randomization. Although subjects younger than 8 years of age may be affected by osteoporosis, limited normative data prevents assignment of a BMD Z score for this group.
- Regarding subjects with child-bearing potential Females who have had at least one menstrual cycle must either be abstinent or must be using an effective method of birth control.
Exclusion
- Current or recent (within 6 months) treatment with therapeutic doses of a bisphosphonate, calcitonin, human growth hormone, and heparin, all agents known to alter bone density
- A history of recent (within one year of screening) major upper gastrointestinal (GI) disease (above the jejunum), including, but not limited to, peptic ulcer, esophageal disease or active GI bleeding, or ever had surgery of the upper GI tract other than pyloroplasty. A history of abnormalities of the esophagus which delay esophageal emptying, such as stricture or achalasia
- Hyperthyroidism (suppressed thyroid stimulating hormone (TSH) and elevated free thyroxine (T4)), hyperparathyroidism (elevated parathyroid hormone (PTH)), malignancy, rickets, or osteomalacia (by history), all assessed within 8 weeks of the Baseline Visit.
- 25 (OH) vitamin D below 20 mg/L
- Planned or current pregnancy and/or breastfeeding
- Renal dysfunction defined as dependence on dialysis or a creatinine clearance \< 35 ml/min, assessed within 4 weeks of the Baseline Visit. Creatinine clearance = \[(height in cm x 0.55)/plasma creatinine\] for all females and for males \< 13 years old; \[(height in cm x 0.70)/plasma creatinine\] for males ³ 13 years old.
- Hepatic insufficiency defined as SGPT or SGOT greater than twice normal for age, assessed within 4 weeks of the Baseline Visit.
- Uncorrected hypocalcemia (ionized calcium\>10% below age-adjusted range), assessed within 4 weeks of the Baseline Visit
- Known or suspected hypersensitivity to bisphosphonates
- Inability to follow instructions for dosing, including being unable to swallow the study medication with plain water first thing in the morning, stand or sit upright without any other food or beverage for at least 30 minutes following dosing and until their next meal
- Weight greater than 136 kg (300 lb), as the DXA is not reliable for subjects of this size
- Weight less than 17 kg (37 lb), assessed within 8 weeks of the Baseline Visit
- Permanent foreign body (prosthetic, surgical clips, permanent earring/umbilical ring) in region of results of the study
- Enrollment Procedures interest, or soft tissue calcinosis overlying the region of interest
- Inability to undergo dual energy X-ray absorptiometry or CT scan
- Developmental or cognitive delay which may interfere with cooperation and/or compliance with the procedures
- Subject expects to move out of the area during the study period, rendering follow-up per protocol impractical
Key Trial Info
Start Date :
March 1 2003
Trial Type :
INTERVENTIONAL
End Date :
June 1 2006
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT00277251
Start Date
March 1 2003
End Date
June 1 2006
Last Update
April 11 2017
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.