CClinicalTrials.gg
Not yet recruitingNCT07360457Updated Jan 22, 2026

GLP1 Analogues and the Risk of Osteoarthritis

An observational study in Osteoarthritis, sponsored by Beni-Suef University. Not yet recruiting. Open to participants aged 50 Years and older. Per ClinicalTrials.gov, last updated 2026-01-22.

Sponsored by Beni-Suef University · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
390
Ages
50 Years and older
Sex
All
01

Study summary

Assessing the effects of GLP1 RA Vs SGLT2 Inhibitors vs. Standard of care in joint pain, physical function, stiffness, and improving Quality of Life for patients with type 2 diabetes.

Read the detailed description

Osteoarthritis (OA) is a multifactorial joint disease related to multiple inflammatory pathways which are triggered by mechanical and cellular stress, leading to increased production of pro-inflammatory mediators, reactive oxygen species, advanced glycation end products (AGEs). These mediators promote the release of proteolytic enzymes, which degrade the cartilage matrix. A recent study emphasized on the relation between metabolic syndrome and OA, considering metabolic dysregulation as a major factor in OA progression.

GLP-1 receptor agonists lower blood sugar by boosting glucose-dependent insulin release, reducing glucagon secretion, and slowing stomach emptying. GLP-1RA is present in both healthy and osteoarthritic cartilage, indicating a direct effect on chondrocytes. so it can decrease the accumulation of AGEs, which is the main cause of OA. It also reduces appetite, leading to weight loss which decreases the mechanical stress on joints. GLP downregulates proinflammatory cytokines (IL-6, TNF-a). also inhibits NF-κB pathway. which has a role in promoting osteoclast formation, so GLP plays a protective role in OA.

02

Conditions studied

  • Osteoarthritis

Browse trials for

Keywords

  • GLP-1
03

In context

Osteoarthritis

4,398 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.

This study's planned enrollment of 390 is above the median of 100 across 791 observational studies indexed under Osteoarthritis.

Browse Osteoarthritis studies →

Lead sponsor

Beni-Suef University is the lead sponsor of 333 studies on the registry; 116 are open to participants now.

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

04

Who can participate

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

Study population

130 T2DM patients will be admitted in each group Group 1 : T2DM patients receiving SGLT2 inhibitors for at least 1 year added to their standard of care Group 2: T2DM patients receiving GLP1 analogues for at least 1 year added to their standard of care Group 3: T2DM patients receiving only standard of care

Inclusion criteria

  • Adults aged above 50 years old with a previous diagnosis of T2DM according to ADA 2025, who have been on either SGLT2 inhibitors or GLP-1 analogs for at least one year.

Exclusion criteria

Exclusion Criteria:

  • individuals with Type 1 Diabetes Mellitus
  • non-diabetic individuals
  • those taking prandial insulin
  • patients with arthritis without osteoarthritis,
  • those taking other medications contraindicated with study medications,
  • pregnant or breastfeeding females
  • those allergic to active ingredients,
  • those using corticosteroids, Autoimmune disease patients or patients receiving immunotherapies, monoclonal antibody targeting TNF-α or IL-6.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
390 participants (estimated)
Patient registry
No

Groups and cohorts

  • SGLT2 Group

    T2DM patients receiving SGLT2 inhibitors for at least 1 year added to their standard of care

    Drug: SGLT2 inhibitor

  • GLP1 Group

    T2DM patients receiving GLP1 analogues for at least 1 year added to their standard of care

    Drug: GLP-1 analog

  • Control group

    T2DM patients receiving only standard of care

    Drug: Antidiabetic

Interventions

  • DrugGLP-1 analog

    glucagon like peptide analogues

    Also known as: GLP1 receptor agonist

  • DrugSGLT2 inhibitor

    sodium glucose transporter-2 inhibitors

    Also known as: gliflozin

  • DrugAntidiabetic

    Standard of care

    Also known as: Control

06

What researchers measure

Primary outcomes

  1. WOMAC score

    A validated, self-administered questionnaire used to assess pain, stiffness, and physical function

    Time frame: at Day 1

Secondary outcomes

  1. VAS pain score

    numerical measure to assess pain

    Time frame: at Day 1

07

Study locations

No study locations are listed for this record.

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 Jan 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07360457
Lead sponsor
Beni-Suef University
Responsible party
Asmaa Abdelfattah Elsayed (Lecturer of clinical pharmacy, Beni-Suef University) — Principal investigator
First posted
Jan 22, 2026
Start date
Feb 1, 2026 (estimated)
Primary completion
Dec 1, 2026 (estimated)
Completion
Mar 1, 2027 (estimated)
Last update
Jan 22, 2026

Study contacts

Asmaa A Elsayed
Contact
asmaa.abdelfattah@pharm.sohag.edu.eg
01095727201
Asmaa Elsayed
principal investigator · Sohag University

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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