ClinicalTrials.gg
RecruitingNCT07490184Updated Aug 4, 2026

Cardiac Clearance vs G60 Hip Frailty Index

An observational study in Cardiac Disease, sponsored by Methodist Health System. Recruiting at 1 site in United States. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2026-08-04.

Sponsored by Methodist Health System · Observational

From the registry’s dates

  • Started Jan 2024; still recruiting 2 years 9 months later.

Help build ClinicalTrials.gg — short surveys, remote interviews or testing, in your language. Take part →

Study type
Observational
Model
Other
Time perspective
Other
Enrollment
100
Ages
60 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-13

Among 646 studies in Heart Diseases with a site in United States — 93 open to participants now, 131 under way, 5 of them phase 3. Heart Diseases · United States.

Planned enrollment
139th of 206
100 · median 300
Started
2024
with 29 others
Observational
211 of 646
32 open now
Primary completion
2027-02
later than 43 of 128 live
Registered
635th of 646
by date

Among the 646 studies in Heart Diseases with a site in United States, this one is the 139th largest by planned enrollment of the 206 observational ones that give a count, is one of 30 that started in 2024, is one of 211 observational ones, reaches primary completion later than 43 of the 128 other live ones, and was the 635th registered.

Heart Diseases

2,135 studies on the registry are indexed under Heart Diseases; 252 are open to participants now.

Browse Heart Diseases studies →

Open to participants now

93 of the 646 studies in Heart Diseases with a site in United States are open now. Recruiting first, the newest first:

88 more — sign in →

All 93 open studies →

A study can be open while its sites in United States have not opened yet or have stopped. Only those recruiting at a site in United States →

Who these studies take

Of the 181 Heart Diseases studies recruiting now, 128 (71%) set no upper age limit and 21 (12%) stop at 75 or younger; 32 take children under 18; 42 take healthy volunteers.

This study: 60 Years and older · all sexes · no healthy volunteers.

The full table on the hub →

This tab as a report to print or save as PDF → With an account.

Was this useful?
Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 646 studies in Heart Diseases with a site in United States, or all of them as a file.
02

Study summary

The primary objective of this study is to establish a data repository that will be permissive of quality improvement studies/observations specific to postoperative mortality outcomes for geriatric patients with orthopedic injuries based on Orthopedic Hip Frailty Score and preoperative cardiac clearance predictors.

Read the detailed description

It is typically a result of advanced aging. Among geriatric patients suffering from hip fractures, frailty is common and is associated with an increased risk of postoperative complications and morbidity with hip fracture surgery. Developed by the Swedish National Quality Registry, the Orthopedic Hip Frailty Score aims to predict short-term postoperative mortality in geriatric patients with hip fractures in order to improve patient outcomes and better allocate resources.

03

Conditions studied

  • Cardiac Disease

Browse trials for

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Among geriatric patients suffering from hip fractures, frailty is common and is associated with an increased risk of postoperative complications and morbidity with hip fracture surgery.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

≥60 years old Included in the Methodist Dallas Medical Center Trauma Registry Documented orthopedic injury with surgical management

Exclusion criteria

Exclusion Criteria:

\<60 years old Prisoners, pregnant persons, or other protected populations

05

Study design

Observational model
Other
Time perspective
Other
Enrollment
100 participants (estimated)
Patient registry
No

Groups and cohorts

  • Total Number and Description of Study Sites/Total Number of Subjects Projected

    This study will include all geriatric trauma patients at Methodist Dallas Medical Center who meet registry inclusion and have an operative orthopedic injury. Enrollment will terminate once five years of data are captured: January 2018 through December 2023.

    Other: Medical/Phenotype Data Collection Procedures & Data to be Collected

Interventions

  • OtherMedical/Phenotype Data Collection Procedures & Data to be Collected

    The Methodist Dallas Medical Center Trauma Registry will be queried for demographic information, diagnosis codes, admission dates, traumatic injury characteristics, surgical procedures, comorbidities, inpatient outcomes, complications, consultations, discharge location, and mortality.

06

What researchers measure

Primary outcomes

  1. Total Number of Study Sites

    This study will include all geriatric trauma patients at Methodist Dallas Medical Center who meet registry inclusion and have an operative orthopedic injury. Enrollment will terminate once five years of data are captured: January 2018 through December 2023.

    Time frame: 5 years

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Yes — All information will be blinded in compliance with Good Clinical Practice. The investigator will make all possible efforts to ensure compliance with all policies regarding sharing of protected health information or research information. Only de-identified protected health information will be shared in relevant research mediums.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Jan 2024 (actual). Primary completion is estimated for Feb 2027, 37 months after the start.

Of 184 non-industry observational studies under Heart Diseases, half reached primary completion within 49 months of starting (the median), counting those still running; a quarter within 22 and three quarters within 118. This study's planned 37 months is below that.

Counting every sponsor, half of 238 studies reached it within 46 months; a quarter within 18 and three quarters within 95.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 18, 2026
First posted
Mar 24, 2026
StartActual
Jan 30, 2024
Primary completionEst.
Feb 2027
CompletionEst.
Feb 2028
Last update
Aug 4, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 4, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07490184
Responsible party
Sponsor
First posted
Mar 24, 2026
Start date
Jan 30, 2024
Primary completion
Feb 2027 (estimated)
Completion
Feb 2028 (estimated)
Last update
Aug 4, 2026

Study contacts

Crystee Cooper, DHEd
Contact
ClinicalResearch@mhd.com
214-947-1280
Kavya Mankulangara
Contact
ClinicalResearch@mhd.com
214-947-4604
Jennifer Burris, MD
principal investigator · Methodist Health System

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion