search
Back to results

Metformin Effect on Fracture Healing in Post-Menopausal Women

Primary Purpose

Bone Fracture

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Metformin Retard 850 mg
Placebo
Sponsored by
Damanhour University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bone Fracture focused on measuring Bone Fracture, Post-Menopausal Women, Metformin, Irisin

Eligibility Criteria

55 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age range from 55 to less than 65 years old with bone fracture.

Exclusion Criteria:

  • Age equal or less than 55 years
  • Age equal or more than 65 years
  • Unstable or hospitalized patients with heart failure
  • Hepatic impairment
  • Chronic kidney disease with eGFR <45 mL/minute/1.73 m2
  • Open fractures
  • Pathological fractures
  • Diabetic patients

Sites / Locations

  • Damanhour Medical National Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Metformin

Placebo

Arm Description

20 post-menopausal women with a bone fracture treated with metformin Retard 850 mg once daily for two weeks then 850 mg twice daily for three months.

20 post-menopausal women with a bone fracture treated with placebo once daily for two weeks then twice daily for three months.

Outcomes

Primary Outcome Measures

Human Irisin (ng/ml)
myokine/adipokine
Bone specific alkaline phosphatase (IU/L)
isoenzyme produced by osteoblasts involved with calcification of skeleton and bone formation
postoperative X-rays - Lane and Sandhu radiological scoring system
evaluate the degree of new bone formation in the fracture line on anterior-posterior and lateral radiographs

Secondary Outcome Measures

Full Information

First Posted
February 15, 2019
Last Updated
February 5, 2021
Sponsor
Damanhour University
search

1. Study Identification

Unique Protocol Identification Number
NCT03845153
Brief Title
Metformin Effect on Fracture Healing in Post-Menopausal Women
Official Title
Study of Metformin Drug Effect on Fracture Healing in Post-Menopausal Women and Its Correlation to Serum Irisin Myokine Level.
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2019 (Actual)
Primary Completion Date
January 1, 2021 (Actual)
Study Completion Date
January 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Damanhour University

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
study the effect of metformin drug on fracture healing of patients with high risk of delayed fracture healing or non-union and correlating this to serum irisin myokine level.
Detailed Description
Approval will be obtained from Ethics Committee of general organization of teaching hospitals and institutes and Research Ethics Committee of Faculty of Pharmacy, Damanhour University. Getting informed consent from all participants to take part in this study. Two groups each of 20 post-menopausal women with a bone fracture. One group will be treated randomly with metformin Retard 850 mg once daily for two weeks then 850 mg twice daily. The other group will be untreated and served as control group. Venous blood samples will be taken from each patient before fracture stabilization and later for determination of serum irisin level with corresponding radiological evaluations. Inclusion criteria: • Age range from 55 to less than 65 years old with bone fracture. Exclusion criteria: Age equal or less than 55 years Age equal or more than 65 years Unstable or hospitalized patients with heart failure Hepatic impairment Chronic kidney disease with eGFR <45 mL/minute/1.73 m2 Open fractures Pathological fractures Diabetic patients Statistical tests appropriate to the study design will be conducted to evaluate the significance of the results. Methodology: Active Human Irisin ELISA kit will be used. Bone-specific Alkaline phosphatase BAP Serum creatinine, serum albumin, prothrombin time. Fasting insulin, fasting blood glucose and Calcium level. BMI, weight, waist, waist-hip ratio, total cholesterol and low-density-lipoprotein cholesterol. radiological scoring system will be used to evaluate the degree of new bone formation in the fracture line on anterior-posterior and lateral radiographs will be taken two months post stabilization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Fracture
Keywords
Bone Fracture, Post-Menopausal Women, Metformin, Irisin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
40 post-menopausal women with a bone fracture divided into two groups each of 20, randomly assigned to administration with metformin Retard 850 mg once daily for two weeks then 850 mg twice daily or with placebo.
Masking
ParticipantOutcomes Assessor
Masking Description
double-blind perspective study
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metformin
Arm Type
Active Comparator
Arm Description
20 post-menopausal women with a bone fracture treated with metformin Retard 850 mg once daily for two weeks then 850 mg twice daily for three months.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
20 post-menopausal women with a bone fracture treated with placebo once daily for two weeks then twice daily for three months.
Intervention Type
Drug
Intervention Name(s)
Metformin Retard 850 mg
Other Intervention Name(s)
Glucophage
Intervention Description
tablet
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
placebo tablet
Primary Outcome Measure Information:
Title
Human Irisin (ng/ml)
Description
myokine/adipokine
Time Frame
three months
Title
Bone specific alkaline phosphatase (IU/L)
Description
isoenzyme produced by osteoblasts involved with calcification of skeleton and bone formation
Time Frame
three months
Title
postoperative X-rays - Lane and Sandhu radiological scoring system
Description
evaluate the degree of new bone formation in the fracture line on anterior-posterior and lateral radiographs
Time Frame
two months post stabilization.

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
post-menopausal women
Minimum Age & Unit of Time
55 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age range from 55 to less than 65 years old with bone fracture. Exclusion Criteria: Age equal or less than 55 years Age equal or more than 65 years Unstable or hospitalized patients with heart failure Hepatic impairment Chronic kidney disease with eGFR <45 mL/minute/1.73 m2 Open fractures Pathological fractures Diabetic patients
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gamal Omran, Professor
Organizational Affiliation
Damanhour University
Official's Role
Study Director
Facility Information:
Facility Name
Damanhour Medical National Institute
City
Damanhūr
State/Province
El-Bahairah
ZIP/Postal Code
31527
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Metformin Effect on Fracture Healing in Post-Menopausal Women

We'll reach out to this number within 24 hrs