Skip to content

Studying the effectiveness of Moqal Azraq cream on pain severity and functional status of plantar fasciitis

Evaluating the effectiveness of Moqal Azraq cream versus corticosteroid injection on pain intensity and functional status of plantar fasciitis: an experimental clinical study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160627028664N5
Enrollment
112
Registered
2025-05-20
Start date
2025-06-20
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

plantar fasciitis. XIII Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention 1: Intervention group: Use of Moqal Azraq cream, which will be 2 cm from the tube of cream, which will be rubbed on the main point of pain and about 5 square centimeters around it twice a

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with plantar fasciitis (as diagnosed by a physician) with pain and localized tenderness of the sole of the foot, especially in the morning, or unilateral or bilateral heel spurs that have not responded to routine medical treatments (physical rest, nonsteroidal painkillers, medical insoles). Their illness history is less than one year. Have a pain score of at least 2 out of 10 VAS points

Exclusion criteria

Exclusion criteria: History of systemic inflammatory disease such as rheumatoid arthritis History of direct trauma with or without fractures of the plantar bones Heel pain associated with Achilles bursitis or myofascial pain in the calf muscles The presence of active radiculopathy that largely explains the cause of plantar fascia pain

Design outcomes

Primary

MeasureTime frame
Pain monitoring score using VAS questionnaire. Timepoint: At the beginning of the study, 4 and 8 weeks after the intervention. Method of measurement: VAS questionnaire.;Foot function questionnaire score. Timepoint: At the beginning of the study and 4 and 8 weeks after the start. Method of measurement: Foot function questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzam Meyari

Hamedan University of Medical Sciences

d_a_meyari@yahoo.com+98 81 3263 3255

Outcome results

None listed

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