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Early Physiotherapy Helps Orthopedic Surgery Patients Recover Faster and Reduce Complications A Clinical Study

Effect of Early Physiotherapy versus Standard Care on Multi-System Complications in Postoperative Orthopedic Surgery Patients: Randomized Controlled Trial (RCT) - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111816
Enrollment
50
Registered
2026-06-03
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Health Condition 1: M968- Other intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified

Interventions

Intervention1: Early Physiotherapy Intervention: Participants in Group A will receive early, structured physiotherapy intervention initiated within 24 72 hours postoperatively and continued for a peri

Sponsors

Uttar Pradesh University of Medical Sciences Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing orthopedic trauma-related surgical procedures, including fractures, joint dislocations, ligament reconstruction, and soft tissue surgeries. Patients in the early postoperative phase (within 48 72 hours after surgery). Patients aged between 18 and 65 years. (Ponkilainen V et al., 2022). [24] Both male and female patients. Medically stable and cleared by the treating surgeon to participate in physiotherapy. Patients able to understand and follow instructions for the physiotherapy program. Patients willing to adhere to the treatment protocol and attend all scheduled sessions. Patients providing written informed consent prior to participation.

Exclusion criteria

Exclusion criteria: Patients with pre-existing respiratory disorders (e.g., chronic obstructive pulmonary disease, bronchial asthma, or other severe pulmonary conditions). Patients with systemic conditions (e.g., uncontrolled diabetes mellitus, severe peripheral vascular disorders, or active infection). Patients with neurological impairments (e.g., stroke, peripheral neuropathy, or altered sensorium) that may affect participation or outcome assessment. Medically unstable patients in whom physiotherapy intervention cannot be safely administered or outcomes cannot be reliably assessed. Patients who are unwilling or unable to provide informed consent.

Design outcomes

Secondary

MeasureTime frame
1. Edema Outcome Measure: Circumferential Limb Measurement (cm) Outcome Details: Edema measured using non-elastic measuring tape at standardized anatomical landmarks around affected limb (cm). 2. Respiratory Function Outcome Measure: Chest Expansion (cm) Outcome Details: Chest expansion measured using measuring tape at axillary/xiphoid level, difference between maximal inspiration and expiration (cm). 3. Pressure Ulcer Status Outcome Measure: PUSH Tool Score (0-17) Outcome Details: PUSH Tool (Pressure Ulcer Scale for Healing): surface area (0-10), exudate (0-3), tissue type (0-4), total 0-17 ordinal scale, lower score = better healing.Timepoint: T0 (Day 1/baseline), T1 (Day 4), T2 (Day 10 or discharge, whichever is earlier)

Primary

MeasureTime frame
REEDA Scale (0-15) and Wound Size (cm ) using Smartphone Digital Planimetry Outcome Details: Wound healing assessed using REEDA Scale (Redness, Edema, Ecchymosis, Discharge, Approximation; each scored 0-3 ordinal scale, total 0-15, lower score = better healing, and wound size measured using smartphone-based digital planimetry (cm ) with high-resolution photographs at standardized 30 cm distance and 1 cm calibration gridTimepoint: T0 (Day 1/baseline), T1 (Day 4), T2 (Day 10 or discharge, whichever is earlier)

Countries

India

Contacts

Public ContactADITI GUPTA

Uttar Pradesh University of Medical Sciences

potturigowrishankar@gmail.com9603803011

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026