RecruitingNot ApplicableNCT06987175

Effects of Sedante Neo Therapy on Pain, Range of Motion and Quality of Life in Patients With Non Specific Low Back Pain.


Sponsor

Riphah International University

Enrollment

40 participants

Start Date

May 15, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

this study is to evaluate the effects of SADANTE neo therapy on pain, range of motion and quality of life in patients with non-specific low back pain.


Eligibility

Min Age: 20 WeeksMax Age: 40 Weeks

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Conventional exercises and sadante neo therapy for people with low back pain, pain, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 20 Weeks to 40 Weeks.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERsadante neo therapy

SAN machine having 3 tube cords on both sides. Each tube cord contains 2 pairs of flat suction cups. We will use 4 pair of flat suction cups in this study. We will place 2 pair on left and two on right para spinal muscles of lumber in prone lying. Due to its automatic suctioning capability, these cups can easily stick to skin. After placing the cups on lumber each patient of group A will receive its stimulation for about 10 minutes every day for about 4 weeks along with conventional exercises.

OTHERConventional exercises

receive conventional exercises only. Conventional exercises will be performed for 20 minutes, each exercise will be performed 20 times with 10 seconds hold.


Locations(1)

Arthritis and pain care clinic Lahore.

Lahore, Punjab Province, Pakistan

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06987175


Related Trials