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CompletedNCT03845153Updated Feb 9, 2021

Metformin Effect on Fracture Healing in Post-Menopausal Women

A Phase 4 interventional study of Metformin Retard 850 mg and Placebo in Bone Fracture, sponsored by Damanhour University. Completed at 1 site in Egypt. Open to female participants aged 55 Years to 65 Years. Per ClinicalTrials.gov, last updated 2021-02-09.

Sponsored by Damanhour University · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
55 Years to 65 Years
Sex
Female
01

Study 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.

Read the detailed description
  1. 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.
  2. Getting informed consent from all participants to take part in this study.
  3. 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.
  4. 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.
02

Conditions studied

  • Bone Fracture

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Keywords

  • Bone Fracture
  • Post-Menopausal Women
  • Metformin
  • Irisin
03

In context

Fractures, Bone

2,261 studies on the registry are indexed under Fractures, Bone; 325 are open to participants now.

This study's enrollment of 40 is below the median of 69 across 1,482 interventional studies indexed under Fractures, Bone.

Browse Fractures, Bone studies →

Lead sponsor

Damanhour University is the lead sponsor of 76 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
55 Years to 65 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

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
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
40 participants (actual)

Study arms

  • Active comparator
    Metformin

    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.

    Drug: Metformin Retard 850 mg

  • Placebo comparator
    Placebo

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

    Other: Placebo

Interventions

  • DrugMetformin Retard 850 mg

    tablet

    Also known as: Glucophage

  • OtherPlacebo

    placebo tablet

06

What researchers measure

Primary outcomes

  1. Human Irisin (ng/ml)

    myokine/adipokine

    Time frame: three months

  2. Bone specific alkaline phosphatase (IU/L)

    isoenzyme produced by osteoblasts involved with calcification of skeleton and bone formation

    Time frame: three months

  3. 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

    Time frame: two months post stabilization.

07

Study locations

1 site
  • Damanhour Medical National Institute
    Damanhūr, El-Bahairah 31527, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03845153
Lead sponsor
Damanhour University
Responsible party
Rehab Werida (Principal Investigator, Damanhour University) — Principal investigator
First posted
Feb 19, 2019
Start date
Jan 1, 2019
Primary completion
Jan 1, 2021
Completion
Jan 1, 2021
Last update
Feb 9, 2021

Study contacts

Gamal Omran, Professor
study director · Damanhour University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2021. You cannot join it, but the record below documents what was studied.

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