Skip to content

Effect of IASTM vs intermittent pneumatic compression therapy as an adjunct to manual lymphatic drainage in orthopedic post-surgical lower limb edema: a randomised controlled trial

Effect of IASTM vs intermittent pneumatic compression therapy as an adjunct to manual lymphatic drainage in orthopedic post-surgical lower limb edema: a randomised controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/103778
Enrollment
60
Registered
2026-02-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: M96-M96- Intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Group A:Manual Lymphatic Drainage: TOTAL DURATION:20 to 30 minutes PATIENT POSITION The patient is positioned in supine lying with the lower limb slightly elevated using a pillow under

Sponsors

Irfan Khan
Lead Sponsor

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

MeasureTime 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

MeasureTime 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

Public ContactIrfan Khan

KLE INSTITUTE OF PHYSIOTHERAPY

santoshmetgud@klekipt.edu.in9880088400

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026