Effects of Phonophoresis with Diclofenac Diethylamine on cervical spondylosis

EFFECTS OF PHONOPHORESIS WITH AND WITHOUT DICLOFENAC DIETHYLAMINE WITH ROUTINE PHYSICAL THERAPY ON PAIN AND RANGE OF MOTION IN PATIENTS WITH CERVICAL SPONDYLOSIS

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20240713062426N1

Enrollment

Registered

2024-07-25

Start date

2024-02-01

Completion date

Unknown

Last updated

2024-08-26

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

Conditions

Cervical Spondylosis. Spondylosis without myelopathy or radiculopathy, cervical region

Interventions

Intervention 1: Intervention group:. Intervention 2: Control group:.

Eligibility

Sex/Gender

All

Age

30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients of both genders of age range from 30-60 years Pre-diagnosed cases of cervical spondylosis with and without radiculopathy Patients referred by orthopedic surgeons. Patients who are diagnosed with cervical spondylosis by other professionals/doctors.

Exclusion criteria

Exclusion criteria: Patients with cervical fracture. Patients with vertebrobasilar insufficiency Presence of other significant rheumatic disease variants. Patients who have history of any cervical spine surgery. Patients who have active infection. Pregnant Females Ankylosing Spondylitis

Design outcomes

Primary

Measure	Time frame
Functional Disability. Timepoint: Before intervention and at the 2nd and 4th weeks after intervention. Method of measurement: Neck Disability Index.;Pain. Timepoint: Before intervention and at 2nd and 4th weeks after intervention. Method of measurement: Visual Analogue Scale.;Quality of Life. Timepoint: Before intervention and at 2nd and 4th weeks after intervention. Method of measurement: 36-Item Short Form Survey (SF-36).;Range of Motion. Timepoint: Before intervention and at 2nd and 4th weeks after intervention. Method of measurement: Goniometer.	—

Measure

Time frame

Functional Disability. Timepoint: Before intervention and at the 2nd and 4th weeks after intervention. Method of measurement: Neck Disability Index.;Pain. Timepoint: Before intervention and at 2nd and 4th weeks after intervention. Method of measurement: Visual Analogue Scale.;Quality of Life. Timepoint: Before intervention and at 2nd and 4th weeks after intervention. Method of measurement: 36-Item Short Form Survey (SF-36).;Range of Motion. Timepoint: Before intervention and at 2nd and 4th weeks after intervention. Method of measurement: Goniometer.

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Countries

Pakistan

Contacts

Public ContactSara Khatoon

The University of Lahore

sarakhatoon4.sk@gmail.com+92 333 4104427

Outcome results

None listed

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