Skip to content

Which Works Better for Upper Trapezius Trigger Points when applied MFR & IC or Cryostretching & MET

Comparative Study on the Effectiveness of Myofascial Release and Ischemic Compression vs Cryostretching and Muscle Energy Technique in the Management of Upper Trapezius Trigger Points - CUTT Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/105966
Enrollment
100
Registered
2026-03-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: M638- Disorders of muscle in diseases classified elsewhere

Interventions

Intervention1: Myofascial Release and Ischemic Compression + Cryostretching and Muscle Energy Technique: Myofascial Release applied to the upper trapezius using sustained manual pressure and longitudi

Sponsors

Self funded
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Presence of any neurological disorders History of shoulder or neck surgery Diagnosed with severe psychiatric illnesses bone related diseases tumors or infections Diagnosed with cervical radiculopathy, myelopathy, or disc herniation Local skin infections, open wounds, or recent injections in the treatment area Currently undergoing other physiotherapy treatments for neck or shoulder Pregnancy

Exclusion criteria

Exclusion criteria: Presence of any neurological disorders History of shoulder or neck surgery Diagnosed with severe psychiatric illnesses bone related diseases tumors or infections Diagnosed with cervical radiculopathy, myelopathy, or disc herniation Local skin infections, open wounds, or recent injections in the treatment area Currently undergoing other physiotherapy treatments for neck or shoulder Pregnancy Previous traumatic injuries involving the upper limb or cervical spine (e.g., fractures or dislocations) Other systemic conditions such as thyroid issues, cardiac, pulmonary diseases, etc.

Design outcomes

Primary

MeasureTime frame
Reduction in pain intensity measured using VAS scaleTimepoint: Reduction in pain intensity measured using VAS scale

Secondary

MeasureTime frame
Improvement in cervical lateral flexion range of motion measured using a universal goniometerTimepoint: Baseline (Day 0) and End of Week 2

Countries

India

Contacts

Public ContactDr Bhumika Chibber

Amity university, noida

bchhibber@amity.edu9899223561

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Apr 4, 2026