ClinicalTrials.Veeva

Menu

Knee Steroid Injection and Blood Sugar Signatur

The University of Texas System (UT) logo

The University of Texas System (UT)

Status

Completed

Conditions

Diabetes
Knee Osteoarthritis

Treatments

Drug: 40 mg Triamcinolone acetonide

Study type

Observational

Funder types

Other

Identifiers

NCT04317404
STU 2019-1202

Details and patient eligibility

About

A prospective, observational study assessing the relationship between HbA1c level and the post-injection blood glucose signature. Participants will be non-diabetic, pre-diabetic, non-insulin dependent and insulin dependent type 2 diabetic patients who will be receiving a knee steroid injection. All of them will be consented a week prior to the injection, when the CGM sensor will be applied to the back of the upper arm. This will be removed a week after the injection. KOOS survey as well as VAS will be administered. Adverse events (e.g., change in medication or hospitalization) will be monitored throughout the study.

Enrollment

11 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients at the Parkland Outpatient Clinic
  • Indication for unilateral knee joint steroid injection for the treatment of knee joint osteoarthritis

Exclusion criteria

  • Less than 18 years old
  • HbA1c > 12.0%
  • steroid exposure in the 3 months prior to Visit 1
  • 3 or more steroid injections in the preceding 12 months
  • known contraindication to steroid injection (adverse reaction or allergy, active infection, INR > 3.0)
  • lack of improvement with prior knee steroid injection
  • change in diabetic medication regimen in the last 1 month
  • significant change in diet within the last 1 month
  • current use of aspirin
  • allergy to adhesive
  • planned MRI, XR, or CT during the 2-week study period

Trial design

11 participants in 3 patient groups

Diabetic with Knee Osteoarthritis
Description:
HbA1c between 6.5% - 12.0% in the 3 months prior to Visit 1
Treatment:
Drug: 40 mg Triamcinolone acetonide
Pre-diabetic with Knee Osteoarthritis
Description:
HbA1c between 5.6% - 6.4% in the 3 months prior to Visit 1
Treatment:
Drug: 40 mg Triamcinolone acetonide
Non-diabetic with Knee Osteoarthritis
Description:
HbA1c \< 5.6% in the 3 months prior to Visit 1
Treatment:
Drug: 40 mg Triamcinolone acetonide

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems