Therapeutic Area

Orthopedics

Musculoskeletal and joint disease clinical research — device trials, regenerative therapies, and biologic agents, managed with expert PRO scoring and surgical protocol coordination.

Initiate an Orthopedics Trial
Overview

Musculoskeletal Trials, From Design to Close-out.

Mayomi Research Solutions manages orthopedic and musculoskeletal clinical trials across osteoarthritis, rheumatoid arthritis, osteoporosis, bone regeneration, and surgical device studies. Our team is experienced in coordinating trials that require surgical site visits, perioperative data collection, imaging-based endpoints, and long-term follow-up assessments.

We provide specialist support for Patient Reported Outcome (PRO) instruments including WOMAC, KOOS, VAS pain scales, and SF-36, as well as radiological assessment coordination for joint space narrowing measurements and bone density evaluations (DEXA).

  • Osteoarthritis (knee, hip, shoulder) trials
  • Rheumatoid & psoriatic arthritis studies
  • Bone regeneration & fracture healing research
  • Orthopaedic device & implant (Class C) trials
  • Biologics (anti-TNF, anti-IL-17, JAK inhibitors) for joint disease

At a Glance

Trial Phases Phase II, III, IV
Regulatory Bodies CDSCO, FDA, EMA, CDSCO Device
Key Endpoints WOMAC, KOOS, VAS, ACR20/50/70, JSN
Patient Population Adults with chronic joint/bone disorders
Study Types RCT, Double-blind, Surgical parallel-arm
Location Bengaluru, Orthopaedic hospitals
Trial Capabilities

What We Deliver.

Specialized capabilities built for the unique demands of orthopedic and musculoskeletal clinical research.

Joint & Bone Device Trials

End-to-end coordination of CDSCO Class C orthopaedic device studies including surgical site qualification, intraoperative data collection, and post-implantation safety follow-up.

PRO & Functional Scoring

Standardised administration and quality review of WOMAC, KOOS, Oxford Knee Score, and VAS pain instruments across investigator sites, ensuring endpoint accuracy and missing data minimisation.

Post-Market Surveillance

Structured post-market clinical follow-up (PMCF) studies for orthopaedic implants and devices, supporting CE mark maintenance and CDSCO regulatory commitments.

Get Started

Initiate an Orthopedics Trial.

Contact our clinical operations team to discuss your musculoskeletal trial design, surgical site requirements, and device regulatory strategy.

Contact Our Team