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The effect of Tecar therapy on haematoma caused by hamstring muscle strain

Comparison of TENS current, Ultrasound and exercise with/without Tecar therapy on muscle haematoma, pain, pain pressure threshold and quality of life in Hamstring muscle strain injury

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191022045187N1
Enrollment
32
Registered
2019-12-27
Start date
2019-04-09
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Muscle Strain Injury. Strain of muscle, fascia and tendon of the posterior muscle group at thigh level

Interventions

Intervention 1: Intervention group: Patients in this group receive Capacitive Tecar therapy ( High frequency electromagnetic currents), with intensity of 20-30 percent for 15 minutes in injury site o

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Age 18-40 Structural hamstring muscle strain injuries ( indirect muscle injuries) Existence of muscle haematoma which is confirmed by imaging test Patients with pain intensity of more than 3, in Visual Analog Scale Absence of history of surgery or metal implantation in lower limb, especially in posterior area of hip and thigh Not using Analgesic and Anticoagulant drugs

Exclusion criteria

Exclusion criteria: Pregnancy Existence of tumor or malignant tissue Having electronic implanted device such as pace maker Open infected wounds Treated with radiotherapy in last 6 month Cardiovascular disorders Tuberclosis Unreliable patients

Design outcomes

Primary

MeasureTime frame
Area size of muscle haematoma. Timepoint: Before intervention, After 10 treatment sessions, After 1 and 2 month follow up. Method of measurement: Ultrasonography imaging.

Secondary

MeasureTime frame
Pain intensity. Timepoint: Before intervention, After 10 treatment sessions, After 1 and 2 month follow up. Method of measurement: Based on Visual Analog Scale.;Pain Pressure Threshold. Timepoint: Before intervention, After 10 treatment sessions, After 1 and 2 month follow up. Method of measurement: By using Algometer device.;Quality of life. Timepoint: Before intervention, After 10 treatment sessions, After 1 and 2 month follow up. Method of measurement: Using SF-36 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Ali Adabi

Shahid Beheshti University of Medical Sciences

aliadabi_msc@yahoo.com+98 21 3624 7842

Outcome results

None listed

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