Early Partial Weight-bearing May Improve Functional Recovery Without Increasing Complications Despite This Potential, Limited Randomized Studies Have Evaluated Early Weight-bearing After Pelvic Fixation Surgeries

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-55
SponsorAssiut University

About this trial

The goal of this randomized clinical trial is to compare between the effect of immediate weight bearing (WB) versus delayed weight bearing in improving function, pain, gait, quality of reduction radiologically, muscle strength, and quality of life outcomes in individuals who underwent specific pelvic fixation surgeries.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 to 55 years

Traumatic fractures indicated for pelvic fixation.

All Types B after stable anterior and / or posterior fixation.

Disqualifiers

Associated lower extremity fractures that independently restrict or contraindicate weight-bearing activities.

Bilateral unstable after fixation pelvic ring disruption.

Patients with associated spinal cord injury, as neurological deficits may alter gait, functional recovery, and weight-bearing capacity, thereby affecting the validity and generalizability of the outcome measures.

Current history of acute systemic infection, active Bone inflammatory disease, (e.g., osteomyelitis, chronic non-bacterial osteitis), or malignancy, which may compromise the healing process, confound clinical outcomes, or pose additional medical risks during rehabilitation.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Immediate Partial Weight Bearing

    Other intervention

    Immediate Partial Weight Bearing

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: weight bearingExperimental treatment 1 intervention
Group B: non-weight bearingNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Functional status

Functional status will be evaluated with the Majeed Pelvic Score

Time frame
at 12 weeks and at 18 weeks

Secondary outcomes

1

core and hip muscle strength

core and hip muscle strength, trunk (flexors, extensors and lateral flexors) and hip (extensors and abductors) using VALD handheld dynamometer

Time frame
at 6 weeks and at 12 weeks
2

Pain level

Pain rating using numerical pain rating scale (NPRS)

Time frame
1st day, 6 weeks , 12 weeks, 18 weeks
3

Gait

Gait by (Functional Gait Assessment)

Time frame
At 18 weeks
4

Radiological outcome

Radiological outcome, loss of reduction, by x-ray

Time frame
1st day post-operative, 6 weeks, 12 weeks, 18 weeks

Other outcomes

Sponsors and contacts

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