Study of the effects of a yoga procedure that is Brahmamudra and Anutaila Nasya in patient of cervical spondylosis

Not yet recruiting

Conditions: Diseases of the musculoskeletal system and connective tissue,

Registration Number: CTRI/2018/09/015828

Lead Sponsor: NA

Brief Summary: Standard controlled trial of Brahmamudra and Anutaila Nasya in management of cervical spondylosis. Total 60 patient of cervical spondylosis who will be attending Swasthrakshan OPD and IPD will be selected irrespective of gender, religion, economical status, education and occupation etc Participants will be selected from both sexes, age ranging between 20 to 50 years presenting with pain related to cervical spondylosis. The study shall have two arms viz. Brahmamudra and arm Anu tail Nasya arm. 2 DROPS of Anutail Nasya will be advised daily for 30 days to Group A and 10-15 rotation of Brahmamudra will be advised daily for duration of 30 days to Group B. Assessment shall be done as per Visual Analogue Scale (VAS) and Neck pain disability index questionnaire and Range of cervical movement by goniometry.

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 60

Inclusion Criteria

1.Prediagnosed cervical spondylosis patient.
2.Age group between 20 to 50 years irrespective of gender, cast or religion.
3.Patients ready to give written informed consent.

Exclusion Criteria

1.Patient with congenital anomaly of spine 2.Patient with fracture or dislocation of cervical vertebrae and intervertibral disc 3.Patient of accidental cases 4.Patient with long term steroidal and hormonal treatment 5.Patient with fracture or dislocation of cervical spine, spondolylolythesis and any other anatomical deformities.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Mean change in Goniometry	Day 0 and Day 30
2.Visual analogue scale	Day 0 and Day 30
3.Neck pain disability index questionnaire	Day 0 and Day 30

Secondary Outcome Measures

Name	Time	Method
Adverse Event	Day 0 and Day 30

Trial Locations

Locations (1): P.D.E.A. College for Ayurved and Research Centre
🇮🇳
Pune, MAHARASHTRA, India
P.D.E.A. College for Ayurved and Research Centre
🇮🇳Pune, MAHARASHTRA, India
VdFarhatunnisa A AZIZ Syed
Principal investigator
7083786676
drfarhat.yogayurved@gmail.com