Skip to content

Effect of ultrasound in MTP 1 injection

ultrasound_guided vs blind stroid injection in patient with MTP pain

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180731040647N2
Enrollment
50
Registered
2019-06-25
Start date
2019-03-21
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

MTP pain. M77.4

Interventions

Intervention 1: Intervention group:In this group of 40mg of methyl prednisolone from the Abouiryhan Pharmaceutical Company for injection into metatarsophalangeal joint is used in the first visit under

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: At least 18 years old A history of MTP pain during rest or walking that lasts for at least 3 months. Having a VAS score of at least 3 before entering the study Pain at the dorsal of the first MTP Radiographic evidence of OA as a reduction in articular space or formation of steophyte (grade 1.2)

Exclusion criteria

Exclusion criteria: Patient's willingness to leave the study at each stage of the plan Lack of access to the patient for post-intervention examination due to lack of personal referral The patient's desire to use systemic steroid or intra-articular injection, except for the injectable substance studied by the patient during the study period Radiographic evidence of severe osteoarthritis (grade 3) Previous history of MTP surgery History of any MTP injections within the past six months Use of modality in physiotherapy in the last 3 months Do not have the ability to walk for daily routine (> 50 m) without the assistive device. There is a risk factor for intra-articular injection such as anticoagulant Presence of poor control diabetes, coagulation disorders, fractures, rheumatologic diseases, tumors and infections and gout Pregnancy or the decision to become pregnant Severe deformity of the MTP joint Acute trauma (last 3 months)

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: The beginning of the study and 6-2 weeks after the injection. Method of measurement: VAS questionnaire.

Secondary

MeasureTime frame
Score patient status. Timepoint: In the beginning of the study, and 2-6 weeks after the injection of the drug. Method of measurement: American Orthopedic Foot and Ankle Society Score (AOFAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Emami Razavi

Tehran University of Medical Sciences

Zemamirazavi@gmail.com+98 21 6658 1420

Outcome results

None listed

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