Skip to content

Treatment of heel pain by Hijama (cupping)

Evaluating the comparative efficacy of Hijamah bil Shart and Hijamah bila Shart in reducing the impact of Plantar Fasciitis - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071696
Enrollment
60
Registered
2024-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: M722- Plantar fascial fibromatosis Health Condition 2: M722- Plantar fascial fibromatosis Health Condition 3: M722- Plantar fascial fibromatosis

Interventions

Intervention1: Wet cupping (hijamah bil shart) : 30 patients will be included for wet cupping for 4 visits in 20 days from baseline to 10 and 20 days and fourth visit 15 days after the end of study pr

Sponsors

Govt.tibbi college and hospital,Patna
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients of all genders 2.Patients of age group 18-60 yrs 3.Clinically diagnosed patients 4.Clinically stable patients

Exclusion criteria

Exclusion criteria: 1.Unstable, bed ridden and mentally retard patients. 2.Patients less than 18 year and more than 60 years of age group. 3.Patients having blood disorders like hemophilia, sickle cell anemia, thalassemia etc. 4.Extreme obese and diabetic patient (with healing disorders) 5.Patients having congenital disability in foot like high arched foot or flat foot Calcanean/heel spurs 6.Ligament/tendon injury/sprain around heel/ankle joint. 7.Traumatic (fracture or dislocation at ankle joints) patients. 8.Patients having malignancy 9.Pregnant and lactating women. 10.Patients having damaged blood vessels locally, DVT and Dermatomyositis (connective tissue disease). 11.Patients having local wounds and severe infection. 12.Patients who do not report for follow up. 13.Patient who does not willing to participate in the study.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale(VAS) Plantar fasciitis pain scale(PFPS) Timepoint: 20 days

Secondary

MeasureTime frame
Heel pain Tenderness Morning Stiffness Restriction of Movement (ROM) Timepoint: 20 days

Countries

India

Contacts

Public ContactTanveer Alam

Government tibbi college and hospitalPatna

tanveernium3133@gmail.com7543854407

Outcome results

None listed

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