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Effectiveness of Dural Tube Myofascial Release in Cervicogenic Headache: Randomized Controlled Trial

Effectiveness of Dural Tube Myofascial Release on Suboccipital Muscle Thickness, Cervical Flexion-Rotation Range & Clinical Metrics For Cervicogenic Headache: Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077197
Enrollment
34
Registered
2024-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention1: Dural Tube Release: Dural Tube release given for a duration of 4 weeks on alternate days followed by SNAGs and Low Load Exercise Control Intervention1: SNAGs and Low Load exercise: SNAG

Sponsors

Aarti Welling
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Individuals diagnosed with CGH based on the CHISG with a mandatory presentation of unilaterality of the head pain without side-shift associated with the neck pain and positive flexion-rotation test less then 33 degrees.31 2.All gender individuals aged 18-50 years. 3.Willingness to participate in the intervention while continuing to follow up for 12 weeks.

Exclusion criteria

Exclusion criteria: 1.Primary headache according to ICHD.9 2.Exhibiting any red flags for manual therapy15 like spinal infection, vertebral tumors or fracture, cervical instability, metabolic diseases, rheumatoid arthritis, osteoporosis, dizziness or visual disturbance symptoms, skin inflammatory condition, ulcers or wounds around treatment area. 3.Any medical or surgical conditions that prevents the participants from going in prone position as it is required for the intervention. 4.Taking prescribed analgesics or physiotherapy or any other allied therapies for the treatment of headache/ cervical pain/ or any other condition within 1 month. 5. Radiating pain in the upper extremity/neurological deficits to the upper extremities or known cases of cervical disc condition, arthritis of the cervical spine. 6.History of central nervous system involvement and vestibular dysfunction. 7.History of prior surgery to the head or neck. 8.Pregnancy.

Design outcomes

Primary

MeasureTime frame
1. Suboccipital Muscle thickness assessment using ultrasonography 2. Flexion Rotation TestTimepoint: Baseline and Post intervention (4 weeks)

Secondary

MeasureTime frame
1. Intensity, Duration and Frequency 2. Quality of lifeTimepoint: Baseline and Post Intervention (4 weeks, 6 weeks and 8 weeks)

Countries

India

Contacts

Public ContactAarti Welling

KLE Institute of Physiotherapy

vijaykage@yahoo.in9845271899

Outcome results

None listed

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