New combo therapy aims to loosen stiff elbows without surgery
NCT ID NCT07598526
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study compares two physical therapy approaches for people with elbow stiffness after a fracture. Thirty participants will either receive Mulligan mobilization alone or combined with myofascial release. Both groups also get heat packs and stretching. The goal is to see which method better reduces pain, improves range of motion, and restores daily function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Mulligan mobilization with myofascial release technique
- What this could lead to
- If it works, this could offer a more effective physical therapy approach for people with stiff elbows after injury.
- What could go wrong
- This is a small, early-stage trial with only 30 participants, so results may not apply to everyone. The treatment is non-invasive, but benefits may be modest.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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17 to 44 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participants aged between 17 and 44 years will be included in the study (Sun et al., 2025). * Both male and female patients experiencing mild to moderate elbow pain (3/10 to 5/10 on NPRS) along with restricted range of motion will be eligible (Zulfqar et al., 2021). * Subjects having elbow movement limitation of more than 30° in extension, flexion less than 120°, and 50° restriction in both pronation and supination will be included (Masci et al., 2020). * Participants will be recruited 3 to 6 weeks after POP removal, and radiographic confirmation of bone/skeletal healing will be ensured before inclusion (Morrey et al., 2017). * Patients with both intra-articular and extra-articular fractures will be considered eligible. * Individuals with DASH scores ranging from 45 to 50 points will be included. * Only patients willing to participate in the study will be enrolled. Exclusion Criteria: * Patients with a history of previous surgical excision will be excluded from the study (Zheng et al., 2018). * Participants presenting with pathological fractures will not be included (Zulfqar et al., 2021). * Patients in the acute stage of fracture will be excluded from participation (Zulfqar et al., 2021). * Individuals with metabolic or malignant conditions causing elbow stiffness, such as gout or osteosarcoma, will not be eligible (Fusaro et al., 2014). * Patients with elbow fractures associated with a history of metal implants will be excluded (Zheng et al., 2018). * Individuals who have already received physiotherapy treatment or medication for the condition will not be included. * Patients diagnosed with psychological illnesses that may interfere with following instructions will be excluded. * Participants with brain trauma or referred neurological symptoms, including numbness, dizziness, or hyperesthesia, will not be considered (Fusaro et al., 2014). * Patients with structural or postural abnormalities involving the shoulder or wrist will be excluded. * Individuals with open skin wounds or burn injuries around the affected area will not be included. * Patients with a pre-operative history of arthritis will also be excluded from the study.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Outdoor Patient Department (OPD) of Madinah Teaching Hospital and Chiniot General Hospital, Faisalabad.
Faisalābad, Punjab Province, 38000, Pakistan
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