Health Condition 1: M96-M96- Intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Adults aged 18 to 65 years, including all genders 2.Patients who have undergone lower limb orthopaedic or reconstructive surgeries involving the hip, knee, or ankle 3.Presence of post-surgical lower limb edema within 1 to 12 weeks following surgery 4.Surgical incision completely healed, with no active wound breakdown or infection 5.Patients who are medically stable and cleared for physiotherapy by the treating surgeon
Exclusion criteria
Exclusion criteria: 1.Presence of active infection, cellulitis, or open wounds in the lower limb 2.Uncontrolled systemic conditions, including hypertension or diabetes mellitus. 3.Peripheral vascular diseases. 4.History of malignancy, lymph node removal, or exposure to radiation therapy. 5.Cardiac conditions that contraindicate physiotherapy or compression-based interventions. 6.Peripheral neuropathies affecting the lower limb. 7.Recent use of complete decongestive therapy within two weeks prior to enrolment. 8.Pregnancy. 9.Known hypersensitivity to any intervention used in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Range of Motion (ROM) using Digital Inclinometer Lower limb joint range of motion will be assessed using a digital inclinometer. The ranges of motion evaluated will include: Knee Flexion, Extension and Ankle Plantarflexion , Dorsiflexion 2.Circumferential Tape Measurement (Edema Assessment) Edema will be assessed using circumferential tape measurement at standardized anatomical landmarks around the involved lower limb. 3.Lower Extremity Functional Scale (LEFS) Functional ability of the lower limb will be evaluated using the Lower Extremity Functional Scale (LEFS). Timepoint: Pre assessment and Post assessment of outcome measures will be done immediately post intervention and after 1 week of follow up | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain Assessment using Numeric Pain Rating Scale (NPRS) Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS). Pain scores will be recorded during the pre-assessment, immediately post-intervention, and after one week of follow-up.Timepoint: Pre assessment and Post assessment of outcome measures will be done immediately post intervention and after 1 week of follow up | — |
Countries
India
Contacts
KLE INSTITUTE OF PHYSIOTHERAPY