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Assess the efficacy of multitarget therapy in prevention of Avascular necrosis (AVN)

A Randomized Controlled Trial (RCT) to assess the efficacy of multitarget therapy in prevention of avascular necrosis (AVN) in patients taking high dose steroid in two groups (case and control)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210808052105N1
Enrollment
70
Registered
2022-01-02
Start date
2022-02-18
Completion date
Unknown
Last updated
2022-01-11

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

Conditions

Osteonecrosis.

Interventions

Intervention 1: Intervention group: Includes patients whose multi-target therapies such as atorvastatin 40 mg daily, vitamin E (400 mg) daily, and aspirin 80 mg daily are added to their bisphosphonate

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with autoimmune connective tissue diseases and vasculitis Requires treatment with high doses of corticosteroids

Exclusion criteria

Exclusion criteria: Co-occurrence of antiphospholipid syndrome Taking drugs that increase the risk of coagulation, such as oral contraceptives Occurrence of events leading to increased coagulation such as long-term hospitalization, trauma leading to surgery Taking anticoagulants Occurrence of adverse drug reactions in the course of patient examination

Design outcomes

Primary

MeasureTime frame
Evidence of Osteonecrosis following high-dose Corticosteroids. Timepoint: In the first three months after starting Corticosteroid and also one year after starting it. Method of measurement: Three-phasic bone scan.

Secondary

MeasureTime frame
Incidence of side effects of drugs. Timepoint: Monthly. Method of measurement: History and Laboratory findings.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Loghman

Tehran University of Medical Sciences

loghmanmaryam@yahoo.com+98 21 8822 0065

Outcome results

None listed

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