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Outcome predictors of ultrasound-guided shoulder hydrodilatation among patients with frozen shoulder;prospective observational analytic study

Outcome predictors of ultrasound-guided shoulder hydrodilatation among patients with frozen shoulder;prospective observational analytic study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20230201001
Enrollment
80
Registered
2023-02-01
Start date
2022-11-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Frozen shoulder patients were done with ultrasound-guided shoulder hydrodilatation technique. frozen shoulder, outcome predictor, prognostic factor, shoulder hydrodilatation

Interventions

the onset of pain or stiffness less than 6 months before performing ultrasound-guided shoulder hydrodilatation.,the onset of pain or stiffness more than 6 months before performing ultrasound-guided sh
Other,Other
early frozen shoulder,late frozen shoulder

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-70 years old 2. Diagnosed with frozen shoulder by clinical diagnosis criteria 3. Physician considered managing by performing shoulder hydrodilatation 4. Consent to additional data collection

Exclusion criteria

Exclusion criteria: 1. DIseases or conditions affected the outcome assessment; history of septic arthritis, trauma at the shoulder area, fracture, history of shoulder surgery, shoulder subluxation or dislocation, rheumatologic disease, OA shoulder, hemiplegic frozen shoulder 2. Recent shoulder hydrodilatation in the past 3 months Withdrawal criteria 1. Received physiotherapy during the study period 2. Received other shoulder intervention during the study period

Design outcomes

Primary

MeasureTime frame
shoulder function baseline, 6 weeks post shoulder hydrodilatation Oxford Shoulder Score, Thai version

Secondary

MeasureTime frame
pain intensity baseline, 6 week post shoulder hydrodilatation VAS,Range of motion baseline, 6 weeks post shoulder hydrodilatation goniometer

Countries

Thailand

Contacts

Public ContactChernkhuan Stonsaovapak

Faculty of Medicine, Chulalongkorn University

chernkhuan@gmail.com6622564433

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026