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Not yet recruitingNCT07729527Updated Jul 29, 2026

Effects of Hyaluronic Acid for Subdeltoid Bursitis

An interventional study of Hyaluronic Acid (HA), 2 ml, single injection in Subdeltoid Bursitis of the Shoulder, sponsored by Shin Kong Wu Ho-Su Memorial Hospital. Not yet recruiting at 1 site in Taiwan. Open to participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2026-07-29.

Sponsored by Shin Kong Wu Ho-Su Memorial Hospital · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
20 Years and older
Sex
All
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Study summary

The study employs a double-blind, randomized clinical trial design with 50 patients diagnosed with subdeltoid bursitis. Participants are divided into two groups: with either cross-linked hyaluronic acid or non-crossed-linked hyaluronic acid injection. All injections are guided by ultrasound. Assessments are conducted before treatment and at 1 week, 1 month, and 3 months post-treatment.

Read the detailed description

Evaluation indicators include pain (measured by Visual Analog Scale, and pain threshold via pressure algometer), function (assessed by Disabilities of the Arm, Shoulder, and Hand score and Shoulder Pain and Disability Index), quality of life (using the World Health Organization Quality of Life-BREF).

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Conditions studied

  • Subdeltoid Bursitis of the Shoulder

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Keywords

  • subdeltoid bursitis
  • hyaluronic acid
  • pain
  • function
  • quality of life
03

In context

Pain

10,054 studies on the registry are indexed under Pain; 1,649 are open to participants now.

This study's planned enrollment of 50 is below the median of 66 across 8,493 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Shin Kong Wu Ho-Su Memorial Hospital is the lead sponsor of 65 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Unilateral shoulder pain within the past 2 weeks Pain during joint movements such as abduction or internal rotation At least one positive result from the following tests: Painful arc, Neer test, or Hawkins test No shoulder injections received in the past 3 months

Willingness to receive injection treatment and undergo follow-up assessments at the following time points:

Immediate (1 week after injection) Short-term (1 month after injection) Mid-term (3 months after injection)

Avoid use of anti-inflammatory painkillers during the study period as much as possible; if intolerable pain occurs, acetaminophen (provided by the researcher) will be used to relieve symptoms

Exclusion criteria

Exclusion Criteria:

Presence of infectious disease, inflammation, rheumatoid arthritis, or fracture History of Previous shoulder surgery Sensory deficits Tendon rupture of the rotator cuff or biceps tendon Neurological disorders causing hand weakness or affecting shoulder mobility (e.g., stroke, Parkinson's disease, brachial plexus injury, peripheral neuropathy) Cognitive impairment preventing completion of questionnaires Cervical radiculopathy Diagnosed frozen shoulder (adhesive capsulitis) Psychiatric disorders Breastfeeding or pregnant women Received shoulder injection within the past 3 months, including , hyaluronic acid, -rich plasma, or any prolotherapy solution

Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

Platelets

Blood cells that help blood clot. Too few raises the risk of bleeding and bruising. A usual adult range is about 150–400 × 10⁹/L (150,000–400,000 per µL); each lab has its own reference range.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    cross-linked hyaluronic acid

    cross-linked acid injection

    Device: Hyaluronic Acid (HA), 2 ml, single injection

  • Active comparator
    Non-crossed linked hyaluronic acid

    non-cross-linked hyaluronic acid injection

    Device: Hyaluronic Acid (HA), 2 ml, single injection

Interventions

  • DeviceHyaluronic Acid (HA), 2 ml, single injection

    hyaluronic acid, 2ml, single injection

06

What researchers measure

Primary outcomes

  1. Shoulder Pain and Disability Index

    A questionnaire to evaluate the severity of shoulder pain and disability in patients with shoulder problems; higher scores indicated more significant pain and disability.The score ranges from 0 to 100: 0 = no disability; 100 = most severe disability

    Time frame: Score change from baseline to 1 week, 1 months and 3 months of treatment, higher score, the better outcome

Secondary outcomes

  1. Disability of the Arm, Shoulder, and Hand

    The questionnaire to measure physical function and symptoms in people with upper-limb disorders, including conditions affecting the shoulder, elbow, wrist, or hand. The score ranges from 0 to 100: 0 = no disability; 100 = most severe disability

    Time frame: Score change from baseline to 1 week, 1 months and 3 months of treatment, higher score, the better outcome

  2. Range of motions of shoulder joint

    Range of motion of the shoulder joint, from 0 to 160, the higher range of motion, the greater function

    Time frame: Score change from baseline to 1 week, 1 months and 3 months of treatment, higher score, the better outcome

  3. World Health Organization Quality of Life

    Assesses 4 key domains: Physical Health, Psychological , Social Relationships and Environment, score ranges 0-100, higher score indicates greater health

    Time frame: Score change from baseline to 1 week, 1 months and 3 months of treatment, higher score, the better outcome

  4. visual analog scale

    Measuring subjective pain intensity, score ranges from 0 to 10 (or 0 to 100 mm, depending on format), the higher score indicates more severe symptom

    Time frame: Score change from baseline to 1 week, 1 months and 3 months of treatment, higher score, the better outcome

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Study locations

1 site
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References and documents

Individual participant data

Plan to share: No — Not decided.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07729527
Lead sponsor
Shin Kong Wu Ho-Su Memorial Hospital
Responsible party
Ru-Lan Hsieh (Professor, Department of Physical Medicine and Rehabilitationj, Shin Kong Wu Ho-Su Memorial Hospital) — Principal investigator
First posted
Jul 27, 2026
Start date
Jul 31, 2026 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Jul 29, 2026

Study contacts

Ru-Lan Hsieh, Dr, MD
Contact
M001052@ms.skh.org.tw
886 + 2-28332211 ext. 2538, 2531
Ru-Lan Hsieh
study chair · Shin Kong Wu Ho-Su Memorial Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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