extra articular dextrose prolotherapy and physiotherapy in ankle tendinopathy

Comparison efficacy of extra articular dextrose prolotherapy with Routine physiotherapy in chronic ankle tendinopathy

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180416039323N2

Enrollment

Registered

2020-10-11

Start date

2020-10-01

Completion date

Unknown

Last updated

2020-11-09

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

Conditions

Ankle Tendinopathy. Unspecified superficial injury of ankle

Interventions

Intervention 1: Intervention group: Physiotherapy treatment study group that include 10 sessions of treatment with Hotpack,Ultrasound,TENS in the affected area is performed. Intervention 2: Interventi

Eligibility

Sex/Gender

All

Age

20 Years to 50 Years

Inclusion criteria

Inclusion criteria: 20<age<50 MRI evidence of tendinopathy conscious patient satisfaction symptoms more than 6 month

Exclusion criteria

Exclusion criteria: rheumatological disease diabetes localized local infection allergy to the drug to be injected use of anticoagulants INR disrupted immunodeficiency acute fracture

Design outcomes

Primary

Measure	Time frame
Evaluation of pain intensity. Timepoint: E??valuation of pain intensity befor ,1 and 3 month after injection or physiotherapy. Method of measurement: Cumperland outcome score questionnaire.;Functional improvement. Timepoint: Evaluation of functional improvment befor ,1 and 3 month after injection or physiotherapy. Method of measurement: Cumperland outcome score questionnaire.;Kinesiophobia. Timepoint: Befor ,1 and 3 month after injection or physiotherapy. Method of measurement: Tampa Scale for Kinesiophobia.	—

Measure

Time frame

Evaluation of pain intensity. Timepoint: E??valuation of pain intensity befor ,1 and 3 month after injection or physiotherapy. Method of measurement: Cumperland outcome score questionnaire.;Functional improvement. Timepoint: Evaluation of functional improvment befor ,1 and 3 month after injection or physiotherapy. Method of measurement: Cumperland outcome score questionnaire.;Kinesiophobia. Timepoint: Befor ,1 and 3 month after injection or physiotherapy. Method of measurement: Tampa Scale for Kinesiophobia.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSanaz Hamidipanah

Artesh University of Medical Sciences

y.hamidihamidi@yahoo.com+98 21 4421 6034

Outcome results

None listed

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