Using Different Doses of Active Vitamin D Combined With Neutral Phosphate in Children With X-linked Hypophosphatemia

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT03820518
Collaborator
(none)
100
1
2
72
1.4

Study Details

Study Description

Brief Summary

X-linked hypophosphatemia (XLH) is the most common form of heritable rickets. Current treatments include active vitamin D metabolites (e.g. calcitriol) and phosphate salts. There is no consistent weight-based dosing of calcitriol and phosphate now. The primary objective of this study is to establish the efficacy of different dose of calcitriol combined with neutral phosphate in children with XLH.

Condition or Disease Intervention/Treatment Phase
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparing the Effectiveness of High or Low Dose of Active Vitamin D Combined With Neutral Phosphate in Children With X-linked Hypophosphatemia
Actual Study Start Date :
Jan 1, 2017
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: High-dose

Receiving 60 ng/kg/day of calcitriol and 30 mg/kg/day of elemental phosphorus.

Drug: Calcitriol
Other Names:
  • Elementary phosphorus
  • Experimental: Low-dose

    Receiving 20 ng/kg/day of calcitriol and 30 mg/kg/day of elemental phosphorus.

    Drug: Calcitriol
    Other Names:
  • Elementary phosphorus
  • Outcome Measures

    Primary Outcome Measures

    1. Change From Baseline to Post-treatment in Severity of Rickets as Measured by Rickets Severity Score (RSS) Total Score [Baseline, Month 12, 24]

      RSS range from 0 to 10, and higher RSS represent severer rickets. It is consisted of score of worst wrist (0-4) and worst knee (0-6). WRIST-score both radius and ulna separately-2 bones × 2 points = 4 points possible KNEE-score both femur and tibia separately Multiply the grade in A by the multiplier in B for each bone, then add femur and tibia scores together A: Grade 1 2 3 B: Multiplier Portion of growth plate affected 0.5 ≤ 1 condyle or plateau 2 condyles or plateaus bones × 1 point × 3 points = 6 points possible Total: 10 points possible Reference:Thacher, T. Radiographic scoring method for the assessment of the severity of nutritional rickets[J]. Journal of Tropical Pediatrics, 2000, 46(3):132-139.

    Secondary Outcome Measures

    1. Changes From Baseline to Post-treatment in Severity of Rickets as Measured by RSS Wrist and Knee Score [Baseline, Month 12, 24]

      RSS range from 0 to 10, and higher RSS represent severer rickets. It is consisted of score of worst wrist (0-4) and worst knee (0-6). WRIST-score both radius and ulna separately-2 bones × 2 points = 4 points possible KNEE-score both femur and tibia separately Multiply the grade in A by the multiplier in B for each bone, then add femur and tibia scores together A: Grade 1 2 3 B: Multiplier Portion of growth plate affected 0.5 ≤ 1 condyle or plateau 2 condyles or plateaus bones × 1 point × 3 points = 6 points possible Total: 10 points possible Reference:Thacher, T. Radiographic scoring method for the assessment of the severity of nutritional rickets[J]. Journal of Tropical Pediatrics, 2000, 46(3):132-139.

    2. Changes From Baseline to Post-treatment in Growth Velocity [Baseline, Month 12, 24]

      Changes From Baseline to Post-treatment in Severity of Rickets as Measured by RSS Wrist and Knee Score

    3. Changes From Baseline to Post-treatment in Serum Total Alkaline Phosphatase (TALP) Levels [Baseline, Month 3, 6, 12, 18, 24]

      Changes From Baseline to Post-treatment in serum ALP

    4. Changes From Baseline to Post-treatment in serum Carboxy-terminal Collagen Crosslinks (CTX) Levels [Baseline, Month 3, 6, 12, 18, 24]

      Changes From Baseline to Post-treatment in serum CTX

    5. Changes From Baseline to Post-treatment in Serum Phosphorus Levels [Baseline, Month 3, 6, 12, 18, 24]

      Changes From Baseline to Post-treatment in Serum Phosphorus Levels

    6. Changes From Baseline to Post-treatment in Severity of Dental Abscess [Baseline, Month 3, 6, 12, 18, 24]

      The frequency and number of dental abscess will be collected by self-report and examed by investigators

    7. Changes From Baseline to Post-treatment in Severity of Bone Pain as Measured by Visual Analog Pain Scales [Baseline, Month 3, 6, 12, 18, 24]

      Visual Analog Pain Scales (VAS) range from 0-10, and higher score represents severer pain

    8. Changes From Baseline to Post-treatment in Severity of Leg Deformities [Baseline, Month 3, 6, 12, 18, 24]

      The longest distance between two sides of thighs, knees, shanks and ankles are measured to evaluate the severity of leg deformities.

    9. Changes From Baseline to Post-treatment in Serum Osteocalcin Levels [Baseline, Month 3, 6, 12, 18, 24]

      Changes From Baseline to Post-treatment in Serum Osteocalcin Levels

    10. Changes From Baseline to Post-treatment in Height [Baseline, Month 3, 6, 12, 18, 24]

      Changes From Baseline to Post-treatment in Height

    11. Changes From Baseline to Post-treatment in Quality of Life as Measured by Patient-reported Outcomes Measurement Information System [Baseline, Month 3, 6, 12, 18, 24]

      Changes From Baseline to Post-treatment in Quality of Life as Measured by Patient-reported Outcomes Measurement Information System

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    1 Year to 12 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male or female, aged 1-12 years, inclusive

    • Diagnosis of XLH by clinical features: serum phosphorus level < 2.5 mg/dl; ALP?; RSS total score ≥2; bowed legs; short stature; family history with appropriate X-linked inheritance

    • Meet at least one of the following: confirmed Phosphate regulating gene with homology to endopeptidases located on the X chromosome (PHEX) mutation in the participant, or serum FGF23 level >30 pg/ml (Kainos assay)

    • Willing to participate the study, and provide an informed consent

    • Able to complete all aspects of study and adhere to the visit schedule

    Exclusion Criteria:
    • Use of growth hormone within 12 months before first visit

    • Height >50 percentile for age and sex specific data

    • Presence of nephrocalcinosis or nephrolithiasis

    • Serum intact parathyroid hormone level>170 pg/ml

    • Plan to receive orthopaedic surgery in 12 months

    • Poor compliance

    • Use of gonadotropin-releasing hormone therapy right now

    • Use of aluminium hydroxide, steroid, acetazolamide or thiazide drugs within 7 days before first visit

    • Not be fit to participant in the study, by the judgement of investigators

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Endocrinology, Peking Union Medical College Hospital Beijing Beijing China 100730

    Sponsors and Collaborators

    • Peking Union Medical College Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Peking Union Medical College Hospital
    ClinicalTrials.gov Identifier:
    NCT03820518
    Other Study ID Numbers:
    • JS-1824
    First Posted:
    Jan 29, 2019
    Last Update Posted:
    Jan 30, 2019
    Last Verified:
    Jan 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 30, 2019