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Comparison between effectiveness of two different molecular weights of hyaluronic acid on shoulder tendinopathy.

A Comparison between subacromial space injections of Low Molecular Weight Hyaluronic Acid (Hyalgan® MW= 500-700 KD) and High Molecular Weight Hyaluronic Acid (Synogel® MW>2000 KD) in Rotator Cuff Tendinopathy.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170608034390N5
Enrollment
56
Registered
2020-01-16
Start date
2018-06-22
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Rotator cuff tendinopathy. Unsp rotatr-cuff tear/ruptr of left shoulder, not trauma.

Interventions

Intervention 1: Intervention group: High MW of Hyaluronic acid (Synogel® MW>2000 KD) injection in subacromial space of shoulder with Codman's (pendulum) Exercises. Intervention 2: Intervention group:

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: Tendinopathy of Rotator Cuff ?Adults (16-70 years) At least 6 weeks from the onset of pain

Exclusion criteria

Exclusion criteria: Pregnant or lactating Women Active systemic rheumatologic disorders Coagulopathies or on anticoagulant medication Diabetes mellitus Active septic disorders or history of cancers or tumors around the site of shoulder joint Use of systemic corticosteroid drugs recently in one month

Design outcomes

Primary

MeasureTime frame
Pain intensity based on visual analogue scale. Timepoint: Measuring the severity of pain at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: Visual Analogue Scale (VAS).

Secondary

MeasureTime frame
Range of Motion (ROM). Timepoint: Measuring the range of motion at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: Goniometer.;Adverse events (e.g., Inflammation in the injection site). Timepoint: Inflammation in the injection site at the first week of study after the injection. Method of measurement: Hyperemia, warmth, pain, tendonitis, tenderness.;The disabilities of the arm, shoulder and hand. Timepoint: Measuring the disabilities of the arm, shoulder and hand at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: The Disabilities of the Arm, Shoulder and Hand (DASH) Questionnaire.;Quality of life. Timepoint: Measuring the Quality of life at the beginning of the study (before the intervention), one week, one month and three months after the injection. Method of measurement: QOL-BREF Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadi Esmaily

Shahid Beheshti University of Medical Sciences

Esmaily_hadi@sbmu.ac.ir+98 21 8820 0118

Outcome results

None listed

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