Intertrochanteric Femur FractureEarly Phase 1NCT07179042
Intertrochanteric Femur Fracture Patients Who Receive Metformin With a Placebo
A Early Phase 1 study testing Metformin in people with Intertrochanteric Femur Fracture and Muscle Atrophy, run by University of Utah at 1 site in United States.
Trial summary
The investigators central hypothesis is that metformin supplementation will be well-tolerated, safe, and provide patients with improved functional and muscle morphology outcomes following intertrochanteric femur fracture. Read more about this study
- Who is it for?
- Ages 60 to 90 years
- Conditions the study is for
- Intertrochanteric Femur Fracture, Muscle Atrophy
- What is being tested?
- Metformin
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 60 participants
- Where
- 1 siteUnited States
- Study dates
- 4 Sep 2025to Sep 2030
- Phase
- Early Phase 1
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 60 to 90 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age 60y and older.
- Displaced hip fracture (femoral neck, intertrochanteric femur, subtrochanteric femur fracture).
- Low energy mechanism of injury (ground level fall, etc).
- Operative treatment within 72 hours of injury.
- Previously ambulatory.
Who cannot join
- History of kidney disease or failure (CKD > stage 4; eGFR < 45 mL/min/1.73m2).
- History of diabetes mellitus (HbA1c > 6.5).
- Associated lower extremity fracture (ipsilateral or contralateral).
- Pathologic fracture.
- Presence of infection at the fracture site.
- History of metabolic bone disease (Pagets, etc.).
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- Severe cognitive impairment (Six Item Screener with 3 or more errors).
- Stage 5 Parkinson's Disease.
- Open fracture.
- Risk of developing metformin-associated hypoglycemia (e.g., hepatic impairment (by history or screening laboratory assessment), presence of hypoglycemia at screening, history of adrenal or pituitary insufficiency, alcohol use disorder, subjects unable to maintain normal oral intake).
- Severe hepatic impairment (Child-Pugh C).
- Expected survival < 6 months (based on clinical judgement).
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
United States1 site
University of Utah Orthopedics
Salt Lake City, Utah, 84108
About this study
Official title: A Pilot Study to Assess the Feasibility of a Randomized, Double-blind, Placebo-controlled Trial Investigating Intertrochanteric Femur Fracture Patients Who Receive Metformin With a Placebo
The investigators central hypothesis is that metformin supplementation will be well-tolerated, safe, and provide patients with improved functional and muscle morphology outcomes following intertrochanteric femur fracture. The objectives will be tested in older adults that sustain a hip fracture and are randomized to receive a daily oral dose (1.5g daily) of metformin or a non-active placebo during 4 months of recovery following surgery.
Read the detailed description
This study team investigates a patient population that undergoes muscle atrophy and falls under the current IND indication of metformin usage to prevent muscle atrophy and enhance muscle growth. The investigators are now proposing to utilize metformin as a novel tool to enhance muscle recovery following a hip fracture in older adults. The investigators currently preparing an IRB protocol in which the investigators plan to perform a pilot study where older adult hip fracture patients are randomized to metformin or placebo. The investigators propose to use metformin to help enhance muscle recovery outcomes in this experimental study design since there are no effective methods to maximize muscle regrowth in older adults following hip fracture.
Hip fracture is a common and costly injury for hundreds of thousands of U.S. older adults every year resulting in devastating health consequences for many. Muscle atrophy is evident at 1 month post-surgery and commonly persists at least 2-6 months afterwards. This is alarming considering that many are considered sarcopenic leaving little muscle reserve to spare to maintain physical function in this population. Consequently, many are not likely to return to pre-fracture functional level one year after fracture. Rehabilitation strategies following hip fracture has remained largely unchanged over the past several decades, suggesting that older adults recovering from hip fracture could benefit from new, innovative approaches that target muscle mass and function.
Local inflammation has received considerable attention as an underlying mechanism contributing to a decline in skeletal muscle health of older adults with physical function deficits. Skeletal muscle inflammation is heightened in older adults and further in older adults who are inactive. Therefore, it is not surprising that the severe physical trauma and associated physical inactivity that accompanies recovery from hip fracture surgery is characterized by a robust muscle inflammatory response as numerous investigators have previously noted. Though inflammation is clearly important for proper muscle regeneration, hyper- and prolonged inflammation can lead to atrophy possibly interfering with muscle and functional recovery in older adults after hip fracture. Indeed, senescent cells, defined as a state of cell-cycle arrest, are a source of inflammation and accumulate in muscle tissue during injury thereby impairing tissue function. Aging further heightens the accumulation of senescent cells due to poor removal by immune cells given that the immune system declines with age.
Metformin has gained attention for exerting pleiotropic effects targeting key hallmarks of aging. However, the role of metformin on regulating muscle cell size and function in patients following hip fracture is unknown. Metformin has recently been shown to lessen cellular senescence burden in a variety of cell and tissue types in experimental cell culture and rodent models. Metformin may preserve muscle mass by activating AMPKα thereby limiting skeletal muscle inflammation through pro-inflammatory pathways such as NFκB and TLR4 signaling. In prior rodent studies, metformin has shown to attenuate muscle atrophy, muscle proteolysis, and fibrosis during muscle wasting conditions. Moreover, metformin has been shown to increase satellite cell proliferation and improve muscle regeneration following burn injury in mice and reduce muscle fibrosis induced by knee joint immobilization in rat. Importantly, the investigators have recently shown that a clinical dose of metformin given to older adults on bed rest was a safe and effective strategy to improve muscle recovery by reducing tissue fibrosis and muscle inflammation and senescent cell accumulation suggesting that such an approach may likewise show promising outcomes in patients recovering from hip fracture surgery.
- Conditions
- Intertrochanteric Femur Fracture, Muscle Atrophy
- Being tested
- Placebo, Metformin
- Keywords
- Intertrochanteric Femur Fracture, Muscle Atrophy, Metformin, Randomized, Double-blind, Placebo-controlled trial
- Medical subject headings
- Muscular Atrophy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PlaceboDrug
Placebo tablets will be dispensed to the participants for 119-days.
MetforminDrug
Also called Glucophage, Glumetza, Riomet, Fortamet, and N,N-dimethylbiguanide
Metformin tablets will be dispensed to the participants for 119-days.
| Study group | Role | What they receive |
|---|---|---|
| Placebo tablets | Placebo comparator | Encapsulated placebo tablets per day (dosage for days 1-7 following the surgery is 500 mg/day, days 8-13 is 1000 mg/day, days 14-119 is 1500 mg/day). Receives: Drug: Placebo |
| Metformin tablets | Experimental | Encapsulated Metformin tablets per day (dosage for days 1-7 following the surgery is 500 mg/day, days 8-13 is 1000 mg/day, days 14-119 is 1500 mg/day). Receives: Drug: Metformin |
What is being measured
The primary outcome is the main question the study is designed to answer.
Mid-thigh size (MTS), (centimeters)
Mid-thigh circumference will be assessed in the participants. These tests will occur during the standard clinical follow-up visits at 2, 8, and 16 weeks. Each participant will have both legs assessed.
Measured: 2-weeks after surgery
Mid-thigh size (MTS), (centimeters)
Mid-thigh circumference will be assessed in the participants. These tests will occur during the standard clinical follow-up visits at 2, 8, and 16 weeks. Each participant will have both legs assessed.
Measured: 8-weeks after surgery
Mid-thigh size (MTS), (centimeters)
Mid-thigh circumference will be assessed in the participants. These tests will occur during the standard clinical follow-up visits at 2, 8, and 16 weeks. Each participant will have both legs assessed.
Measured: 16-weeks after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Sep 2025
- Study start4 Sep 2025
- Primary completionSep 2030 (estimated)
- Study completionSep 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Intertrochanteric Femur FractureStudies of the same condition, open and under way.
- More trials run by University of UtahThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Early Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- University of Utah
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Justin Haller, University of Utah
- Investigators
- Justin Haller, M.D., Principal investigator, University of Utah Orthopaedics
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07179042
- Sponsor's protocol ID
- 189701
- Status last verified
- Apr 2026
- First submitted
- 10 Sep 2025
- Last updated
- 29 Apr 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Pilot Study to Assess the Feasibility of a Randomized, Double-blind, Placebo-controlled Trial Investigating Intertrochanteric Femur Fracture Patients Who Receive Metformin With a Placebo
- ClinicalTrials.gov ID
- NCT07179042
- Acronym / sponsor ID
- 189701
- Conditions
- Intertrochanteric Femur Fracture, Muscle Atrophy
- Keywords
- Intertrochanteric Femur Fracture, Muscle Atrophy, Metformin, Randomized, Double-blind, Placebo-controlled trial
- Phase
- Early Phase 1
- Study type
- Interventional
- Recruitment status
- Enrolling by invitation
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- University of UtahUniversity, hospital or other
- Study start
- 4 Sep 2025 (actual)
- Primary completion
- Sep 2030 (estimated)
- Study completion
- Sep 2030 (estimated)
- First posted
- 17 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The investigators central hypothesis is that metformin supplementation will be well-tolerated, safe, and provide patients with improved functional and muscle morphology outcomes following intertrochanteric femur fracture. The objectives will be tested in older adults that sustain a hip fracture and are randomized to receive a daily oral dose (1.5g daily) of metformin or a non-active placebo during 4 months of recovery following surgery.
Detailed description
This study team investigates a patient population that undergoes muscle atrophy and falls under the current IND indication of metformin usage to prevent muscle atrophy and enhance muscle growth. The investigators are now proposing to utilize metformin as a novel tool to enhance muscle recovery following a hip fracture in older adults. The investigators currently preparing an IRB protocol in which the investigators plan to perform a pilot study where older adult hip fracture patients are randomized to metformin or placebo. The investigators propose to use metformin to help enhance muscle recovery outcomes in this experimental study design since there are no effective methods to maximize muscle regrowth in older adults following hip fracture.
Hip fracture is a common and costly injury for hundreds of thousands of U.S. older adults every year resulting in devastating health consequences for many. Muscle atrophy is evident at 1 month post-surgery and commonly persists at least 2-6 months afterwards. This is alarming considering that many are considered sarcopenic leaving little muscle reserve to spare to maintain physical function in this population. Consequently, many are not likely to return to pre-fracture functional level one year after fracture. Rehabilitation strategies following hip fracture has remained largely unchanged over the past several decades, suggesting that older adults recovering from hip fracture could benefit from new, innovative approaches that target muscle mass and function.
Local inflammation has received considerable attention as an underlying mechanism contributing to a decline in skeletal muscle health of older adults with physical function deficits. Skeletal muscle inflammation is heightened in older adults and further in older adults who are inactive. Therefore, it is not surprising that the severe physical trauma and associated physical inactivity that accompanies recovery from hip fracture surgery is characterized by a robust muscle inflammatory response as numerous investigators have previously noted. Though inflammation is clearly important for proper muscle regeneration, hyper- and prolonged inflammation can lead to atrophy possibly interfering with muscle and functional recovery in older adults after hip fracture. Indeed, senescent cells, defined as a state of cell-cycle arrest, are a source of inflammation and accumulate in muscle tissue during injury thereby impairing tissue function. Aging further heightens the accumulation of senescent cells due to poor removal by immune cells given that the immune system declines with age.
Metformin has gained attention for exerting pleiotropic effects targeting key hallmarks of aging. However, the role of metformin on regulating muscle cell size and function in patients following hip fracture is unknown. Metformin has recently been shown to lessen cellular senescence burden in a variety of cell and tissue types in experimental cell culture and rodent models. Metformin may preserve muscle mass by activating AMPKα thereby limiting skeletal muscle inflammation through pro-inflammatory pathways such as NFκB and TLR4 signaling. In prior rodent studies, metformin has shown to attenuate muscle atrophy, muscle proteolysis, and fibrosis during muscle wasting conditions. Moreover, metformin has been shown to increase satellite cell proliferation and improve muscle regeneration following burn injury in mice and reduce muscle fibrosis induced by knee joint immobilization in rat. Importantly, the investigators have recently shown that a clinical dose of metformin given to older adults on bed rest was a safe and effective strategy to improve muscle recovery by reducing tissue fibrosis and muscle inflammation and senescent cell accumulation suggesting that such an approach may likewise show promising outcomes in patients recovering from hip fracture surgery.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, care provider)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Placebo tablets | Placebo comparator | Drug: PlaceboEncapsulated placebo tablets per day (dosage for days 1-7 following the surgery is 500 mg/day, days 8-13 is 1000 mg/day, days 14-119 is 1500 mg/day). |
| Metformin tablets | Experimental | Drug: MetforminEncapsulated Metformin tablets per day (dosage for days 1-7 following the surgery is 500 mg/day, days 8-13 is 1000 mg/day, days 14-119 is 1500 mg/day). |
Who may qualify
- Ages
- 60 to 90 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Age 60y and older.
- Displaced hip fracture (femoral neck, intertrochanteric femur, subtrochanteric femur fracture).
- Low energy mechanism of injury (ground level fall, etc).
- Operative treatment within 72 hours of injury.
- Previously ambulatory.
Key exclusion criteria (12 listed)
- History of kidney disease or failure (CKD > stage 4; eGFR < 45 mL/min/1.73m2).
- History of diabetes mellitus (HbA1c > 6.5).
- Associated lower extremity fracture (ipsilateral or contralateral).
- Pathologic fracture.
- Presence of infection at the fracture site.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PlaceboPlacebo tablets will be dispensed to the participants for 119-days. | Drug | Placebo tablets |
| MetforminAlso: Glucophage, Glumetza, Riomet, Fortamet, and N,N-dimethylbiguanideMetformin tablets will be dispensed to the participants for 119-days. | Drug | Metformin tablets |
Primary outcome
Mid-thigh size (MTS), (centimeters)
Time frame: 2-weeks after surgery
Mid-thigh circumference will be assessed in the participants. These tests will occur during the standard clinical follow-up visits at 2, 8, and 16 weeks. Each participant will have both legs assessed.
Mid-thigh size (MTS), (centimeters)
Time frame: 8-weeks after surgery
Mid-thigh circumference will be assessed in the participants. These tests will occur during the standard clinical follow-up visits at 2, 8, and 16 weeks. Each participant will have both legs assessed.
Mid-thigh size (MTS), (centimeters)
Time frame: 16-weeks after surgery
Mid-thigh circumference will be assessed in the participants. These tests will occur during the standard clinical follow-up visits at 2, 8, and 16 weeks. Each participant will have both legs assessed.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Apr 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Justin Haller, M.D. principal investigator
University of Utah Orthopaedics
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Early Phase 1 study testing Metformin in people with Intertrochanteric Femur Fracture and Muscle Atrophy, run by University of Utah at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: enrolling by invitation, as of the sponsor's last update on 29 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Early Phase 1 (sometimes called Phase 0) studies give a very small amount of a treatment to a few people, mainly to see how the body handles it.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Mid-thigh size (MTS), (centimeters) (time frame: 2-weeks after surgery). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Apr 2026.