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To evaluate muscle injury using magnetic resonance imaging after an intragluteal injection of Diclofenac sodium 75 mg/1mL

A prospective open label single arm single centre case study of MRI of Dynapar AQ 75 mg/ml IM

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/023010
Enrollment
1
Registered
2020-01-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Dynapar AQ: Diclofenac Sodium 75 mg per 1 ml will be injected for one time only by Intragluteal route Control Intervention1: NIL: NIL

Sponsors

Apollo Hospitals International Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Male above 18 years of age

Exclusion criteria

Exclusion criteria: Contraindications of diclofenac injection

Design outcomes

Primary

MeasureTime frame
to evaluate muscle injury using MRI following a diclofenac 75 mg/1ml intragluteal injectionTimepoint: Magnetic Resonance Imaging will be done at 2, 12, 22, 32, 47, 62, 92, 122, 182, 242 min, as well 7.5 hr after administration

Secondary

MeasureTime frame
to observe any change in the inflammatory biomarkers following a diclofenac 75 mg/1ml intragluteal injectionTimepoint: Magnetic Resonance Imaging will be done at 2, 12, 22, 32, 47, 62, 92, 122, 182, 242 min, as well 7.5 hr after administration

Countries

India

Contacts

Public ContactDr Dushyant Balat

Apollo Hospitals International Ltd

drdushyant.balat@gmail.com9825015055

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026