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Effect of Vitamin D and Denosumab on Bone Remodelling in Women With Postmenopausal Osteoporosis

Primary Purpose

Hypovitaminosis D, Osteoporosis, Postmenopausal, Menopause

Status
Completed
Phase
Not Applicable
Locations
Mexico
Study Type
Interventional
Intervention
Cholecalciferol
Sponsored by
Hospital Regional 1o de Octubre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypovitaminosis D focused on measuring Vitamin D, Postmenopausal Osteoporosis, Denosumab, Hypovitaminosis D, Osteoporosis, Osteopenia

Eligibility Criteria

45 Years - 89 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of postmenopausal osteoporosis or osteopenia in treatment with denosumab 60mg every six months plus calcium carbonate 1.2g/day + vitamin D 800IU/day.
  • Diagnosis of hypovitaminosis D, with serum cholecalciferol values <30ng/dL.

Exclusion Criteria:

  • Incomplete clinical records or clinical records.
  • Age over 70 years.
  • Diagnosis of secondary (hereditary) osteoporosis.
  • History of prolonged use of steroids.
  • Lack of adherence to medical treatment.
  • Diagnosis of cancer.
  • Diagnosis of depression.
  • Diagnosis of Celiac disease or with the presence of alterations in intestinal absorption.
  • Allergies to any of the medications administered.

Sites / Locations

  • Patricia Loranca-Moreno

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Vitamin D 4000 IU

Arm Description

4000 IU of vitamin D were administrated once a day orally and calcium carbonate 1.2 g a day in a single dose.

Outcomes

Primary Outcome Measures

Number of participants with hip T-score improvement at 12 months
It refers to the number of participants who improved their hip T-score at three months after treatment.
Number of participants with lumbar spine T-score improvement at 12 months
It refers to the number of participants who improved their lumbar spine T-score at three months after treatment.
Number of participants with osteoporosis of the hip at 12 months
It refers to the number of participants that present a hip T-score above -2.5 three months after treatment.
Number of participants with osteoporosis of the lumbar spine at 12 months
It refers to the number of participants that present a lumbar spine T-score greater than -2.5 three months after treatment.
Number of participants with osteopenia on the hip at 12 months
It refers to the number of participants that present a hip T-score from -1 to -2.4 three months after treatment.
Number of participants with osteopenia of the lumbar spine at 12 months
It refers to the number of participants that present a lumbar spine T-score from -1 to -2.4 three months after treatment.
Number of participants with normal hip T-score at 12 months
It refers to the number of participants that present a hip T-score below -1 three months after treatment.
Number of participants with normal lumbar spine T-score at 12 months
It refers to the number of participants that present a lumbar spine T-score below -1 three months after treatment.
Number of participants with improvement in serum levels of vitamin D at 12 months
Improvement in serum levels of 25-hydroxy vitamin D [25(OH)D] was considered when serum vitamin D levels increased concerning baseline levels.
Number of participants with clinical remission of hypovitaminosis D at 12 months
Remission of hypovitaminosis D was considered when serum levels of 25-hydroxy vitamin D [25(OH)D] were above 29 pg/ml.

Secondary Outcome Measures

Number of participants with vitamin D sufficiency at 12 months
It refers to the number of participants who reached serum levels of vitamin D above 29 pg/ml after three months of treatment.
Number of participants with vitamin D insufficiency at 12 months
It refers to the number of participants who reached serum levels of vitamin D of 21 to 29 pg/ml after three months of treatment.
Number of participants with vitamin D deficiency at 12 months
It refers to the number of participants who reached serum levels of vitamin D less than 20 pg/ml after three months of treatment.

Full Information

First Posted
May 9, 2022
Last Updated
February 15, 2023
Sponsor
Hospital Regional 1o de Octubre
Collaborators
Universidad Nacional Autonoma de Mexico, National Polytechnic Institute, Mexico
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1. Study Identification

Unique Protocol Identification Number
NCT05372224
Brief Title
Effect of Vitamin D and Denosumab on Bone Remodelling in Women With Postmenopausal Osteoporosis
Official Title
Vitamin D Improves Osteoporosis in Postmenopausal Women With Denosumab Failure
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
June 22, 2020 (Actual)
Primary Completion Date
June 22, 2021 (Actual)
Study Completion Date
June 22, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Regional 1o de Octubre
Collaborators
Universidad Nacional Autonoma de Mexico, National Polytechnic Institute, Mexico

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Denosumab is a monoclonal antibody against RANKL ligand, which is used as an alternative treatment for osteoporosis in patients who have a poor response to first-line antiresorptive therapy. However, discontinuation of denosumab produces a rapid increase in bone turnover, bone loss and potentially increased risk of multiple vertebral fractures.
Detailed Description
76 postmenopausal women from the climacteric clinic of the regional hospital "1o de Octubre" of the Institute of Security and Social Services for State Workers (ISSSTE) were firstly considered, of which 23 presented elimination criteria and only 55 who had received denosumab therapy for an average of 2.5 years without a significant improvement in hip and lumbar spine T-scores were enrolled. First, a general medical evaluation was performed. Serum levels of vitamin D were analysed to find the prevalence of hypovitaminosis D. A bone mineral density test was done to calculate hip and lumbar spine T-scores. Then, vitamin D was administrated daily for one year at a dose of 4,000 IU and the studies were repeated after one year. Statistical analysis was performed using PAST 3.0 and GraphPad Prism 8.4.3. software. The arithmetic median (µ) and standard deviation (S.D.) were calculated using Excel-Word. Graphics were constructed with GraphPad Prism 8.4.3 and tables with Excel Word. Categorical variables were analysed with chi-squared or Fisher exact test depending on the number of participants in each cell. Normality was determined using the Shapiro-Wilk test. To compare two paired samples, the Wilcoxon signed-rank test was utilized. The assigned α value for this study was <0.05. In all cases, if a Montecarlo permutation was available, the exact p-value was taken instead of the raw p-value.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypovitaminosis D, Osteoporosis, Postmenopausal, Menopause
Keywords
Vitamin D, Postmenopausal Osteoporosis, Denosumab, Hypovitaminosis D, Osteoporosis, Osteopenia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
76 participants were considered from the climacteric clinic of the regional hospital "1o de Octubre" of the Institute of Security and Social Services for State Workers (ISSSTE), of which 23 presented elimination criteria, and 55 were included in the study.
Masking
None (Open Label)
Allocation
N/A
Enrollment
55 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D 4000 IU
Arm Type
Experimental
Arm Description
4000 IU of vitamin D were administrated once a day orally and calcium carbonate 1.2 g a day in a single dose.
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol
Other Intervention Name(s)
Histofil®
Intervention Description
4000 IU were administrated once a day for 3 months.
Primary Outcome Measure Information:
Title
Number of participants with hip T-score improvement at 12 months
Description
It refers to the number of participants who improved their hip T-score at three months after treatment.
Time Frame
12 months
Title
Number of participants with lumbar spine T-score improvement at 12 months
Description
It refers to the number of participants who improved their lumbar spine T-score at three months after treatment.
Time Frame
12 months
Title
Number of participants with osteoporosis of the hip at 12 months
Description
It refers to the number of participants that present a hip T-score above -2.5 three months after treatment.
Time Frame
12 months
Title
Number of participants with osteoporosis of the lumbar spine at 12 months
Description
It refers to the number of participants that present a lumbar spine T-score greater than -2.5 three months after treatment.
Time Frame
12 months
Title
Number of participants with osteopenia on the hip at 12 months
Description
It refers to the number of participants that present a hip T-score from -1 to -2.4 three months after treatment.
Time Frame
12 months
Title
Number of participants with osteopenia of the lumbar spine at 12 months
Description
It refers to the number of participants that present a lumbar spine T-score from -1 to -2.4 three months after treatment.
Time Frame
12 months
Title
Number of participants with normal hip T-score at 12 months
Description
It refers to the number of participants that present a hip T-score below -1 three months after treatment.
Time Frame
12 months
Title
Number of participants with normal lumbar spine T-score at 12 months
Description
It refers to the number of participants that present a lumbar spine T-score below -1 three months after treatment.
Time Frame
12 months
Title
Number of participants with improvement in serum levels of vitamin D at 12 months
Description
Improvement in serum levels of 25-hydroxy vitamin D [25(OH)D] was considered when serum vitamin D levels increased concerning baseline levels.
Time Frame
12 months
Title
Number of participants with clinical remission of hypovitaminosis D at 12 months
Description
Remission of hypovitaminosis D was considered when serum levels of 25-hydroxy vitamin D [25(OH)D] were above 29 pg/ml.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Number of participants with vitamin D sufficiency at 12 months
Description
It refers to the number of participants who reached serum levels of vitamin D above 29 pg/ml after three months of treatment.
Time Frame
12 months
Title
Number of participants with vitamin D insufficiency at 12 months
Description
It refers to the number of participants who reached serum levels of vitamin D of 21 to 29 pg/ml after three months of treatment.
Time Frame
12 months
Title
Number of participants with vitamin D deficiency at 12 months
Description
It refers to the number of participants who reached serum levels of vitamin D less than 20 pg/ml after three months of treatment.
Time Frame
12 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of postmenopausal osteoporosis or osteopenia in treatment with denosumab 60mg every six months plus calcium carbonate 1.2g/day + vitamin D 800IU/day. Diagnosis of hypovitaminosis D, with serum cholecalciferol values <30ng/dL. Exclusion Criteria: Incomplete clinical records or clinical records. Age over 90 years. Diagnosis of secondary (hereditary) osteoporosis. History of prolonged use of steroids. Lack of adherence to medical treatment. Diagnosis of cancer. Diagnosis of depression. Diagnosis of Celiac disease or with the presence of alterations in intestinal absorption. Allergies to any of the medications administered.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
María B Brito-Gavilanes, M.D.
Organizational Affiliation
Peri-postmenopause and bone metabolism clinic. Regional Hospital October 1 ISSSTE
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patricia Loranca-Moreno, M.D., M.Sc.
Organizational Affiliation
Peri-postmenopause and bone metabolism clinic. Regional Hospital October 1st ISSSTE.
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Juan M Ocampo-Godínez, M.D., P.hD
Organizational Affiliation
Laboratory of Tissue Engineering, UNAM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Patricia Loranca-Moreno
City
Mexico City
State/Province
Gustavo A. Madero
ZIP/Postal Code
07300
Country
Mexico

12. IPD Sharing Statement

Citations:
PubMed Identifier
28789921
Citation
Tsourdi E, Langdahl B, Cohen-Solal M, Aubry-Rozier B, Eriksen EF, Guanabens N, Obermayer-Pietsch B, Ralston SH, Eastell R, Zillikens MC. Discontinuation of Denosumab therapy for osteoporosis: A systematic review and position statement by ECTS. Bone. 2017 Dec;105:11-17. doi: 10.1016/j.bone.2017.08.003. Epub 2017 Aug 5.
Results Reference
background
PubMed Identifier
28144701
Citation
McClung MR, Wagman RB, Miller PD, Wang A, Lewiecki EM. Observations following discontinuation of long-term denosumab therapy. Osteoporos Int. 2017 May;28(5):1723-1732. doi: 10.1007/s00198-017-3919-1. Epub 2017 Jan 31.
Results Reference
background
PubMed Identifier
30324412
Citation
Kanis JA, Cooper C, Rizzoli R, Reginster JY; Scientific Advisory Board of the European Society for Clinical and Economic Aspects of Osteoporosis (ESCEO) and the Committees of Scientific Advisors and National Societies of the International Osteoporosis Foundation (IOF). European guidance for the diagnosis and management of osteoporosis in postmenopausal women. Osteoporos Int. 2019 Jan;30(1):3-44. doi: 10.1007/s00198-018-4704-5. Epub 2018 Oct 15. Erratum In: Osteoporos Int. 2020 Jan;31(1):209. Osteoporos Int. 2020 Apr;31(4):801.
Results Reference
background
PubMed Identifier
33141482
Citation
Miyoshi A, Kameda H, Nagai S, Nakamura A, Miya A, Takase T, Atsumi T, Miyoshi H. Beneficial effects of switching to denosumab from bisphosphonates or selective estrogen receptor modulators in postmenopausal women with type 2 diabetes and osteopenia/osteoporosis. J Diabetes Investig. 2021 Jul;12(7):1293-1300. doi: 10.1111/jdi.13458. Epub 2020 Dec 13.
Results Reference
background
PubMed Identifier
28892457
Citation
Saag KG, Petersen J, Brandi ML, Karaplis AC, Lorentzon M, Thomas T, Maddox J, Fan M, Meisner PD, Grauer A. Romosozumab or Alendronate for Fracture Prevention in Women with Osteoporosis. N Engl J Med. 2017 Oct 12;377(15):1417-1427. doi: 10.1056/NEJMoa1708322. Epub 2017 Sep 11.
Results Reference
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PubMed Identifier
19671655
Citation
Cummings SR, San Martin J, McClung MR, Siris ES, Eastell R, Reid IR, Delmas P, Zoog HB, Austin M, Wang A, Kutilek S, Adami S, Zanchetta J, Libanati C, Siddhanti S, Christiansen C; FREEDOM Trial. Denosumab for prevention of fractures in postmenopausal women with osteoporosis. N Engl J Med. 2009 Aug 20;361(8):756-65. doi: 10.1056/NEJMoa0809493. Epub 2009 Aug 11. Erratum In: N Engl J Med. 2009 Nov 5;361(19):1914.
Results Reference
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PubMed Identifier
31036625
Citation
Takeuchi T, Tanaka Y, Soen S, Yamanaka H, Yoneda T, Tanaka S, Nitta T, Okubo N, Genant HK, van der Heijde D. Effects of the anti-RANKL antibody denosumab on joint structural damage in patients with rheumatoid arthritis treated with conventional synthetic disease-modifying antirheumatic drugs (DESIRABLE study): a randomised, double-blind, placebo-controlled phase 3 trial. Ann Rheum Dis. 2019 Jul;78(7):899-907. doi: 10.1136/annrheumdis-2018-214827. Epub 2019 Apr 29.
Results Reference
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Effect of Vitamin D and Denosumab on Bone Remodelling in Women With Postmenopausal Osteoporosis

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