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PROactive HEALing in High-Risk Pelvic and Non-hip Lower Extremity Fragility Fractures (PRO HEAL Pilot) (PRO HEAL Pilot)

1 octobre 2026 mis à jour par: University of Calgary

PROactive HEALing in High-Risk Pelvic and Non-hip Lower Extremity Fragility Fractures

Fragility fractures are common in older adults with weakened bone. At least 1 in 3 females and 1 in 5 males will sustain a fragility fracture in their lifetime, and over 80% of fractures in Canadians aged 50 years and older are attributable to osteoporosis. Fractures of the pelvis, acetabulum and lower extremity in this population are associated with delayed healing, loss of reduction, implant failure and the need for secondary surgery. Reported complication rates range from 21.5% to 40%. Efforts to improve outcomes have focused on surgical fixation technique; there is currently no pharmacological treatment given to promote healing of the fracture itself.

Teriparatide is a recombinant form of parathyroid hormone (1-34) that stimulates new bone formation. It is authorized in Canada for the treatment of severe osteoporosis. Its use to promote acute fracture healing is investigational and is not an approved indication. Pre-clinical studies have demonstrated enhanced fracture callus formation and improved mechanical strength of healing bone. Clinical evidence in acute fracture healing is limited and mixed: a randomized trial in distal radius fractures reported a shorter time to cortical bridging, and systematic reviews report positive signals in delayed union and non-union, while a small phase 2 trial in acute pelvic fracture found no difference in radiographic healing at three months, although physical performance improved. That trial was terminated early following withdrawal of study drug supply, leaving it underpowered, and its authors concluded that a larger randomized trial is warranted.

No randomized controlled trial has evaluated Teriparatide for the promotion of fracture healing across pelvic, acetabular and non-hip lower extremity fragility fractures in high-risk older adults. Before such a trial can be designed and appropriately powered, its feasibility must be established.

PRO HEAL Pilot is a prospective, open-label, randomized controlled pilot trial with blinded outcome assessment. Fifty-four participants will be randomized 1:1 to Teriparatide or a no-treatment control. Recruitment is planned over 18 months at the Foothills Medical Centre in Calgary.

Eligible participants are males and females aged 50 years and older who have sustained a low-energy fragility fracture (a fall from five feet or less) of the pelvis, the acetabulum, or the non-hip lower extremity, and who have at least one additional risk factor for delayed fracture healing: diabetes, renal dysfunction, steroid use, current or past smoking, peripheral neuropathy, or peripheral vascular disease. Fractures may be managed operatively or non-operatively. Participants must be able and willing to self-administer daily subcutaneous injections, or have a caregiver able to do so.

Participants randomized to the treatment arm receive Teriparatide 20 mcg by subcutaneous injection once daily for 90 doses, with the first dose administered within five days of randomization and within 21 days of the initial fracture. Participants randomized to the control arm receive no study medication and continue standard clinical care. All participants in both arms receive a single oral loading dose of 50,000 IU vitamin D at randomization, with calcium supplementation or dietary modification to achieve a total daily intake of approximately 1,000 mg.

The primary outcome is feasibility, measured as the mean number of participants recruited per month and assessed against a priori progression criteria. Secondary feasibility outcomes are treatment fidelity, defined as the proportion of participants receiving 80% or more of the trial medication; participant retention; consent rate; and barriers to trial implementation.

Clinical, functional and value-based outcomes will be collected in the same manner as planned for the full-scale trial and reported descriptively. Clinical outcomes include pain, radiographic fracture union, unplanned surgical intervention related to the index fracture, bone mineral density, and 90-day all-cause mortality. Functional outcomes include physical performance, the Olerud Molander Score, PROMIS Mobility, and weightbearing status. Value-based outcomes include healthcare costs, quality of life, length of acute hospital stay, and re-admission.

Participants are followed for six months from randomization, with study visits at 2 weeks, 6 weeks, 12 weeks and 6 months, aligned with routine post-fracture clinical follow-up. Participants receiving Teriparatide are contacted weekly by telephone during the treatment period for adherence and safety monitoring, and serum calcium is measured at every study visit. Clinical outcomes are adjudicated by independent assessors blinded to treatment allocation.

This pilot trial is not powered to detect a difference in clinical efficacy between treatment arms. Its purpose is to determine whether a definitive, full-scale randomized controlled trial is feasible, and to inform its design and sample size.

Aperçu de l'étude

Statut

Pas encore de recrutement

Description détaillée

Background & Rationale At least 1 in 3 females and 1 in 5 males will experience a fragility fracture due to osteoporosis or low bone mass in their lifetime, and over 80% of fractures in Canadians aged 50 and older are attributable to osteoporosis. Older adults with poor bone quality who sustain pelvic or lower extremity fragility fractures face high rates of delayed healing, loss of reduction and implant failure, frequently resulting in secondary surgery. Reported complication rates range from 21.5% to 40%, and one-year mortality has been reported as high as 12%. Efforts to improve outcomes have focused on fixation technique; no pharmacological treatment is currently given to promote healing of the fracture itself.

Teriparatide, recombinant parathyroid hormone (1-34), is an anabolic agent authorized in Canada for the treatment of severe osteoporosis. Once-daily administration preferentially stimulates osteoblastic over osteoclastic activity, producing net new bone formation. Pre-clinical studies demonstrate enhanced callus formation and improved mechanical strength of healing bone. Clinical evidence in acute fracture healing is limited and mixed. A randomized trial in distal radius fractures reported shorter time to cortical bridging, and systematic reviews report positive signals in delayed union and non-union. However, a small phase 2 trial in acute pelvic fracture found no difference in radiographic healing at three months, although physical performance improved; that trial was terminated early following withdrawal of study drug supply, was underpowered, and its authors concluded that a larger randomized trial is warranted.

No randomized trial has evaluated teriparatide for fracture healing across pelvic, acetabular and non-hip lower extremity fragility fractures in high-risk older adults. Feasibility must be established before a definitive trial can be designed.

Research Question & Objectives Is it feasible to conduct a full-scale randomized controlled trial comparing teriparatide with no treatment for the promotion of fracture healing in older adults with pelvic, acetabular or non-hip lower extremity fragility fractures? Objectives are to (1) evaluate the feasibility of a definitive full-scale randomized controlled trial, measured by recruitment rate, treatment fidelity, participant retention, consent rate and barriers to trial implementation; and (2) compare complication rates between short-term teriparatide and no treatment, to inform the design and sample size of the full trial. This pilot is not powered to establish efficacy.

Methods Design: prospective, open-label, randomized controlled pilot trial with blinded outcome assessment and 1:1 allocation, conducted at the Foothills Medical Centre.

Population: 54 participants (27 per arm) aged 50 years and older with a low-energy fragility fracture (fall from five feet or less) of the pelvis, acetabulum or non-hip lower extremity, and at least one additional risk factor for delayed healing (diabetes, renal dysfunction, steroid use, current or past smoking, peripheral neuropathy, peripheral vascular disease). Participants must be able and willing to self-administer daily injections, or have a caregiver able to do so, and must provide informed consent or have a surrogate decision maker. Exclusion criteria include recent teriparatide, bisphosphonate or digoxin therapy; hypercalcemia; hypercalciuria; urolithiasis; severe renal impairment; hypersensitivity to teriparatide; and factors conferring elevated osteosarcoma risk. Eligibility bloodwork is reviewed prior to randomization.

Intervention: teriparatide 20 mcg subcutaneously once daily for 90 doses, with the first dose administered within five days of randomization and within 21 days of injury. The comparator arm receives no study medication and continues standard clinical care. All participants in both arms receive vitamin D 50,000 IU at randomization and calcium supplementation to approximately 1,000 mg daily.

Randomization is performed in REDCap using variable block sizes. Participants and treating clinicians are aware of allocation; clinical outcomes are adjudicated by two independent blinded adjudicators, with a third resolving disagreement, using materials from which allocation information has been removed.

Outcomes: the primary feasibility outcome is the mean number of participants recruited per month, assessed against a priori progression criteria. Secondary feasibility outcomes are treatment fidelity, retention, consent rate and implementation barriers. Clinical outcomes include pain, radiographic union, unplanned surgical intervention, bone mineral density and mortality. Functional outcomes include physical performance, the Olerud Molander Score and PROMIS Mobility.

Follow-up occurs at 2, 6 and 12 weeks and 6 months post-randomization, aligned with routine clinical visits. Participants receiving teriparatide are telephoned weekly for safety and adherence monitoring. Serum calcium is measured at every study visit. Analysis is descriptive and conducted on an intention-to-treat basis. Recruitment is planned over 18 months.

Participants randomized to the treatment arm receive teriparatide 20 mcg by subcutaneous injection once daily for 90 doses. This is an investigational use of a marketed drug and is not part of standard care for fracture management.

All participants, in both arms, receive a single oral loading dose of 50,000 IU vitamin D at randomization, with calcium supplementation or dietary modification to approximately 1,000 mg daily.

The following study procedures are additional to standard practice:

  • Eligibility bloodwork prior to randomization (serum calcium, alkaline phosphatase, creatinine, 25-hydroxy vitamin D), where not already obtained as part of clinical care
  • A pregnancy test prior to randomization for participants of childbearing potential
  • Serum calcium at each follow-up visit, drawn from a morning sample, as a safety measure
  • Bone mineral density scan by DEXA at baseline and at 3 months, where a scan within the preceding 6 months is not already available
  • Physical performance testing at follow-up visits (4-metre walk speed, repeated chair stands, balance)
  • Questionnaires at follow-up visits (Olerud Molander Score, PROMIS Mobility, EQ-5D, pain visual analogue scale)
  • Weekly telephone contact during the 90-day treatment period, for participants in the treatment arm, to assess adherence and safety
  • A participant-maintained drug diary, and return of used and unused study medication at each visit

Study visits are aligned with routine post-fracture clinical follow-up at 2 weeks, 6 weeks, 12 weeks and 6 months. Radiographic assessment of healing uses imaging obtained as part of routine clinical care. No additional imaging is performed for research purposes other than the bone mineral density scans described above.

Type d'étude

Interventionnel

Inscription (Estimé)

54

Phase

  • Phase 2
  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Lieux d'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

50 ans et plus (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria Males and females ≥50 years old with a low-energy fragility fracture (fall from 5 feet or less) of the pelvis (one or more ramus fracture and/or sacral fracture[s]), fracture of the acetabulum, or non-hip lower extremity fragility fracture (femur, tibia, fibula)

Participants must have at least one of the following:

  1. Diabetes (insulin dependent or non-insulin dependent)
  2. Renal dysfunction (abnormal creatinine or eGFR that does not meet criteria for "severe impairment" outlined in exclusion criteria)
  3. Steroid use (minimum 5mg prednisone or equivalent daily for >1 month in the last 3 months)
  4. Current smoker
  5. Smoking history (more than six months consecutively within the last 10 years)
  6. Peripheral neuropathy
  7. Peripheral vascular disease

Able/willing to self-administer daily injections or have a caregiver able/willing to administer daily injections Patients providing informed consent or have surrogate decision makers who provide surrogate consent.

Exclusion Criteria Teriparatide, bisphosphonate, or digoxin therapy within the last six months.

Pre-existing diagnosis of any of the following:

Hypercalcemia (total calcium >2.6mmol/L) Hypercalciuria (urine calcium >350mg/24h specimen) Urolithiasis Severe renal impairment (eGFR <30mL/min/1.73m^2, or on dialysis) Serum creatinine greater than 1.5 x the upper limit of normal for age and sex (<150umol/L in females, >180umol/L in males) Known hypersensitivity to teriparatide

Individuals at high risk for osteosarcoma based on pre-existing:

Hyperparathyroidism or Paget's disease Current bone metastases or history of skeletal malignancies Elevated levels of alkaline phosphatase (>180U/L; 1.5 x the upper limit of normal) Prior radiation of the skeleton (external beam or implant) Pregnancy, breastfeeding, or, for participants of childbearing potential, an unwillingness to use effective contraception for the duration of the treatment period.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Teriparatide

20 µg subcutaneous Teriparatide injection once daily for 3 months in the post-operative ankle fracture population.

20 µg subcutaneous (SC) Teriparatide injection

Autres noms:
  • Tériparatide
Aucune intervention: Non-treatment

No treatment control arm

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Participant recruitment rate
Délai: 2 years

Estimate of the mean monthly recruitment rate

2 years

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Treatment fidelity
Délai: 6 months post randomization

Proportion of participants randomized to Teriparatide who receive 80% or more of the trial medication. Determined from a participant-maintained drug diary, weekly telephone confirmation, and return of used and unused study medication pens at each follow-up, recorded at each visit until trial medication is completed. Assessed against a priori progression criteria: green (proceed) greater than 50%; amber (amend) 20% to 50%; red (stop) less than 20%.

6 months post randomization
Participant retention rate
Délai: 6 months post randomization

Proportion of enrolled participants who complete the pilot trial protocol or reach a study endpoint, reported at each follow-up timepoint. Assessed against a priori progression criteria: green (proceed) greater than 80%; amber (amend) 40% to 80%; red (stop) less than 40%.

6 months post randomization
Consent Rate
Délai: 18 months (recruitment period)

Proportion of screened patients who meet eligibility criteria and provide informed or surrogate consent, together with the reasons recorded for non-consent among otherwise eligible patients.

18 months (recruitment period)
Barriers to trial implementation
Délai: Through study completion, approximately 24 months

Descriptive assessment of barriers encountered during trial conduct, comprising time to receive Research Ethics Board approval, time required for contract completion, time from approvals to first participant enrolled, data capture and study management barriers, study team infrastructure challenges, participant-level and site-level challenges, intervention-related challenges, longitudinal study design challenges, and the frequency and nature of protocol deviations.

Through study completion, approximately 24 months
Time to fracture union
Délai: 6 months post randomization.

Time from randomization to radiographic fracture union, assessed on imaging obtained as part of routine clinical care. Long bone fractures are scored using the modified Radiographic Union Scale for Tibia (mRUST). For pelvic and acetabular fractures, where no validated radiographic union score is established, healing is assessed as the presence or absence of radiographic union. All assessments are adjudicated by two independent reviewers blinded to treatment allocation, with a third blinded reviewer resolving disagreement.

6 months post randomization.
Non-union
Délai: 6 months post randomization

Proportion of participants with non-union, defined as failure to achieve radiographic union within six months of randomization, or intervention required for failure to heal. Assessed by blinded adjudication as described for time to fracture union.

6 months post randomization
Unplanned surgical intervention
Délai: 6 months post-randomization

Proportion of participants undergoing unplanned surgical intervention related to the index fracture, with the indication for surgery recorded. Among participants managed operatively, this includes re-operation for implant failure, loss of reduction, non-union or malunion.

6 months post-randomization
Fracture-related infection
Délai: 6 month post randomization

Proportion of participants requiring oral antibiotics, intravenous antibiotics, or surgical debridement for infection related to the index fracture.

6 month post randomization
Bone mineral density
Délai: Baseline and 3 months post-randomization

Bone mineral density measured by dual-energy x-ray absorptiometry (DEXA). A scan performed within six months prior to randomization may be used as the baseline measurement; where no such scan is available, baseline DEXA is performed within 14 days of randomization. A repeat scan is performed at three months post-randomization, corresponding to the end of the treatment period.

Baseline and 3 months post-randomization
Intervention-related complications
Délai: 12 weeks (treatment period)

Proportion of participants experiencing complications attributable to the study intervention, comprising local injection site irritation, hypercalcemia, and intolerance of study medication. Serum calcium is measured at every study visit from a morning sample drawn before that day's dose of study medication.

12 weeks (treatment period)
All-cause mortality
Délai: 90 days post-randomization

Proportion of participants who die from any cause, with cause of death recorded.

90 days post-randomization

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Publications générales

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

15 mars 2027

Achèvement primaire (Estimé)

16 décembre 2030

Achèvement de l'étude (Estimé)

17 mars 2031

Dates d'inscription aux études

Première soumission

4 mars 2024

Première soumission répondant aux critères de contrôle qualité

4 mars 2024

Première publication (Réel)

12 mars 2024

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

6 octobre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

1 octobre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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