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Status unknownNCT05404451Updated Jun 3, 2022

Comparison of Mulligan Mobilization Technique and Mckenzie Exercises Among Patient With Sacroilliac Joint Dysfunction

An interventional study of Mulligan Mobilization and Mckenzie Exercises in Sacroiliac Joint Somatic Dysfunction, sponsored by Superior University. Status unknown at 1 site in Pakistan. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2022-06-03.

Sponsored by Superior University · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Jun 2022), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study summary

Comparison of Mulligan Mobilization Technique and Mckenzie Exercises Among Patient with Sacroilliac Joint Dysfunction

Read the detailed description

To determine comparison of mulligan mobilization technique and McKenzie exercises in patient with sacroiliac joint dysfunction.

02

Conditions studied

  • Sacroiliac Joint Somatic Dysfunction
03

In context

Lead sponsor

Superior University is the lead sponsor of 253 studies on the registry; 25 are open to participants now.

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Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age between 18 to 65.(29)
  • Both male and female and Pain in low back. (17)
  • Pain in sacroiliac joint (PSIS) with or without radiating to buttocks.(30)
  • With acute/subacute pain within 4-12 weeks of onset and at least three of four clinical tests positive.(14)

Exclusion criteria

Exclusion Criteria:

  • Midline pain in back, Lumber stenosis, Lumber radiculopathy, Spondylolisthesis, Disc related pain, Pregnant females with SIJD(29),Any lower limb pathology or hip fracture, Rheumatoid arthritis(17)
  • History of any orthopedic surgery, and conditions such as ankylosing spondylitis.(14)
  • Spinal leminectomy
  • Arthodesis
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
58 participants (estimated)

Study arms

  • Experimental
    Mulligan Mobilization

    Using the Technique of Mulligan Mobilization

    Diagnostic Test: Mulligan Mobilization

  • Experimental
    Mckenzie Exercises

    Using Mckenzie Exercises

    Diagnostic Test: Mckenzie Exercises

Interventions

  • Diagnostic testMulligan Mobilization

    Using the Technique of Mulligan Mobilization

  • Diagnostic testMckenzie Exercises

    Using Mckenzie Exercises

06

What researchers measure

Primary outcomes

  1. Mulligan Mobilization Technique

    29 Participents with Mobilization applied by a therapist and an active physiological movement to end range applied by the patient. Mulligan mobilization with 10 repetitions; 3 sets. Oswestry disability questionnaire with visual analog scale (0 for minimum and 10 for Maximum pain)

    Time frame: 6 Month

Secondary outcomes

  1. Mckenzie Exercises

    29 Participents with intervention technique Lie down on your stomach. Prop yourself up on your forearms with your shoulders above your elbows, Hold for 2 to 3 minutes, Lower your upper body. Repeat up to eight times a day. Modified Oswestry disability questionnaire with visual analog scale(0 for minimum and 10 for Maximum pain)

    Time frame: 6 Months

07

Study locations

1 site
  • Social Security hospital Manga road Raiwind.,Chaudary Muhammad Akram research and teaching hospital.
    Lahore, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 3, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05404451
Lead sponsor
Superior University
Responsible party
Muhammad Naveed Babur (Principal Investigator, Superior University) — Principal investigator
First posted
Jun 3, 2022
Start date
Jun 2022 (estimated)
Primary completion
Aug 2022 (estimated)
Completion
Nov 2022 (estimated)
Last update
Jun 3, 2022

Study contacts

Zunaira Ahmad, DPT
Contact
dptm-f17-015@superior.edu.pk
+923094596366

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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