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Pes Anserine BursitisNCT07881913

Comparison of Bracing and Eccentric Loading Exercises on Pain Modulation and Functional Improvement in Acute Pes Anserine Bursitis Patients

A study testing Medial-Support Knee Brace and Eccentric Loading Exercise in people with Pes Anserine Bursitis, run by Dr Aneeqa Sultan at 2 sites in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aims to compare the effects of knee bracing and eccentric loading exercises on pain and functional ability in adults with acute pes anserine bursitis. Pes anserine bursitis is a condition affecting the inner side of the knee that can cause pain and difficulty with activities such as walking, climbing… Read more about this study

Who is it for?
Ages 20 to 50 years
Conditions the study is for
Pes Anserine Bursitis
What is being tested?
Medial-Support Knee Brace and Eccentric Loading Exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
2 sitesPakistan
Study dates
20 Oct 2025to 27 Aug 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 50 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Adults aged 20-50 years, both male and female.
  • Patients diagnosed with early-stage pes anserine bursitis based on clinical symptoms and imaging.
  • Body mass index (BMI) between 20 and 35.
  • Pain intensity score between 4 and 7.
  • Participants with or without previous surgeries.

Who cannot join

  • Advanced arthritis or systemic inflammatory conditions, such as systemic lupus erythematosus (SLE).
  • Recent lower-limb fracture.
  • Pregnancy or other considerations that contraindicate physical therapy or bracing.
  • Neurological disorders affecting mobility, such as spinal cord injuries.

Trial locations and contacts

2 sites in 1 country.

Pakistan2 sites
  • Lahore Poly Clinic

    Lahore, Punjab Province

  • M. Ali clinic

    Lahore, Punjab Province

Other trials in Pakistan

About this study

This study aims to compare the effects of knee bracing and eccentric loading exercises on pain and functional ability in adults with acute pes anserine bursitis. Pes anserine bursitis is a condition affecting the inner side of the knee that can cause pain and difficulty with activities such as walking, climbing stairs, and standing up from a chair.

A total of 32 participants will be included in the study and divided into two groups. One group will receive a knee-bracing intervention, while the other group will participate in a structured exercise program involving eccentric loading and strengthening exercises for the muscles around the knee.

Read more

The bracing group will be instructed to wear a properly fitted medial-support knee brace for approximately 6-8 hours daily during weight-bearing activities. The exercise group will perform prescribed exercises three times per week for eight weeks, with exercise intensity adjusted according to individual tolerance.

Pain intensity and knee-related functional ability will be assessed using the Visual Analogue Scale (VAS) and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). Assessments will be conducted before treatment and at the planned follow-up visits to evaluate changes in symptoms and function.

The findings are intended to help determine which intervention provides greater improvement in pain and functional ability in people with acute pes anserine bursitis and may help guide physiotherapy treatment decisions.

Read the detailed description

Pes anserine bursitis is a condition involving irritation or inflammation of the bursa located near the insertion of the sartorius, gracilis, and semitendinosus tendons on the inner side of the knee. It may cause localized pain and tenderness and can limit daily activities, including walking, climbing stairs, standing up from a chair, and performing other movements involving the knee.

Conservative physiotherapy management may include exercise therapy and external support. Exercise therapy aims to improve the strength and functional capacity of the muscles surrounding the knee, while a knee brace may provide support during weight-bearing activities. However, further comparative evidence is needed to determine which approach provides greater improvements in pain and functional ability in patients with acute pes anserine bursitis.

Study objective

The objective of this randomized controlled trial is to compare the effects of knee bracing and eccentric loading exercises on pain intensity and knee-related functional ability in adults with acute pes anserine bursitis. The study is intended to determine whether either intervention provides greater improvement in the measured outcomes.

Study design and treatment groups

The study uses a two-group, parallel randomized controlled trial design. Eligible participants are assigned to one of two intervention groups following screening and informed consent. The planned sample comprises 32 participants, with 16 participants allocated to each group.

Bracing group

Participants assigned to the bracing group receive a properly fitted medial-support knee brace. The prescribed wearing schedule is approximately 6-8 hours daily during weight-bearing activities for eight weeks. Participants are instructed on the correct use and care of the brace.

Eccentric loading exercise group

Participants assigned to the exercise group follow a structured exercise program targeting the muscles surrounding the knee, including the quadriceps and hamstrings. The program includes strengthening and functional exercises, such as leg raises, hamstring curls, and step-ups. Exercises are prescribed three times per week for eight weeks, with three sets of approximately 10-15 repetitions, adjusted according to the participant's tolerance and ability. Exercise intensity progresses gradually as tolerated.

Outcome assessment

Pain intensity is assessed using the Visual Analogue Scale (VAS), and knee-related symptoms and functional limitations are assessed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). These instruments are used to evaluate changes in pain and function over the course of the intervention.

Baseline assessments are performed before treatment. Follow-up assessments are planned to evaluate treatment response and determine whether improvements are maintained. The final assessment schedule should correspond to the actual visits completed and the time points specified in the approved study protocol.

Data analysis

Participant characteristics are summarized using descriptive statistics. Within-group changes and between-group differences in pain and functional outcomes are evaluated using appropriate statistical methods. The choice of statistical tests depends on the distribution of the data, the study design, and the availability of measurements at each assessment time point.

Potential significance

The findings may contribute to the evidence supporting conservative physiotherapy management of acute pes anserine bursitis. Comparing these interventions may help physiotherapists make informed treatment decisions based on improvements in pain and knee-related function.

Being tested
Medial-Support Knee Brace, Eccentric Loading Exercise
Keywords
Pes Anserine Bursitis, Knee Pain, Knee Bracing, Eccentric Loading Exercises, Exercise Therapy, Physiotherapy, Visual Analogue Scale, Western Ontario and McMaster Universities Osteoarthritis Index
Medical subject headings
Bursitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Medial-Support Knee BraceDevice

    Participants will use a medial-support knee brace daily for 6-8 hours during mobility for 8 weeks. The intervention will be used in patients with acute pes anserine bursitis to assess its effects on pain modulation and functional improvement.

  • Eccentric Loading ExerciseBehavioural

    Participants will perform a structured exercise program targeting the quadriceps and hamstring muscles for 8 weeks. Supervised sessions will be conducted three times per week, with 3 sets of 10-15 repetitions. Exercise intensity will progress according to participant tolerance.

Study groups in NCT07881913
Study groupRoleWhat they receive
Bracing GroupExperimentalParticipants will use a medial-support knee brace daily for 6-8 hours during mobility for 8 weeks. The intervention aims to reduce pain and improve functional ability in patients with acute pes anserine bursitis.
Receives: Device: Medial-Support Knee Brace
Eccentric Loading Exercise GroupExperimentalParticipants will receive a structured exercise program targeting the quadriceps and hamstring muscles. Supervised sessions will be conducted three times per week for 8 weeks, with 3 sets of 10-15 repetitions. Exercises will progress from low to moderate intensity according to participant tolerance.
Receives: Behavioral: Eccentric Loading Exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Pain Intensity Measured by the Visual Analogue Scale (VAS)

    Pain intensity will be assessed using the Visual Analogue Scale (VAS) before and after the intervention. Changes in VAS scores will be used to evaluate pain reduction following bracing or eccentric loading exercise in patients with acute pes anserine bursitis.

    Measured: Baseline and after 8 weeks of intervention

Secondary outcomes (1)
  1. Change in Knee Pain and Functional Ability Measured by the WOMAC Index

    Knee-related pain and functional ability will be assessed using the Western Ontario and McMaster Universities Arthritis Index (WOMAC) before and after the intervention. Changes in WOMAC scores will be used to evaluate improvement following bracing or eccentric loading exercise.

    Measured: Baseline and after 8 weeks of intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Oct 2026
  2. Study start20 Oct 2025
  3. Primary completion27 Apr 2026
  4. Study completion27 Aug 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
This is a two-arm, parallel-group interventional study comparing knee bracing with eccentric loading exercises in adults with acute pes anserine bursitis. Participants are assigned to one of the two treatment groups and receive the allocated intervention over an 8-week treatment period.
Masking
None (open label)
Enrolment
32 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07881913
Sponsor's protocol ID
SU-PAB-2026-01
Status last verified
Oct 2026
First submitted
13 Oct 2026
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Medial-Support Knee Brace and Eccentric Loading Exercise in people with Pes Anserine Bursitis, run by Dr Aneeqa Sultan at 2 sites in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Pain Intensity Measured by the Visual Analogue Scale (VAS) (time frame: Baseline and after 8 weeks of intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Oct 2026.

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