CClinicalTrials.gg
Status unknownNCT05810831Updated Apr 12, 2023

Efficacy of Massage Versus Massage With Post Isometric Relaxation Exercises in Temporomandibular Disorders

An interventional study of Massage with post isometric relaxation exercises and Massage in Pain, Joint, sponsored by Superior University. Status unknown. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-04-12.

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

The sponsor has not verified this record recently (last verified Mar 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

To determine effectiveness of massage versus massage with post isometric relaxation exercises in temporomandibular disorders for pain and limited joint mobility.

02

Conditions studied

03

In context

Temporomandibular Joint Disorders

609 studies on the registry are indexed under Temporomandibular Joint Disorders; 160 are open to participants now.

This study's planned enrollment of 46 is close to the median of 46 across 434 interventional studies indexed under Temporomandibular Joint Disorders.

Browse Temporomandibular Joint Disorders studies →

Lead sponsor

Superior University is the lead sponsor of 242 studies on the registry; 24 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • patients with clinical features with myofascial pain and limited mouth opening fulfilling the Axis Group I of RDC/TMD criteria,
  • absence of temporomandibular disc displacement with or without reduction,
  • good general health (absence of chronic diseases which may affect temporomandibular joint or the masticatory muscles),
  • full dental arches with natural teeth or missing teeth replaced with fixed dental prostheses

Exclusion criteria

Exclusion Criteria:

  • earlier splint therapy,
  • pharmacotherapy (e.g., hormone replacement therapy, oral contraception and antidepressants),
  • injury of masticatory organ,
  • undergoing orthodontic treatment,
  • inflammation in oral cavity (e.g., impacted molars and pulp inflammation) and fibromyalgia
05

Study design

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

Study arms

  • Experimental
    Massage with post isometric relaxation exercises

    Diagnostic Test: Massage with post isometric relaxation exercises

  • Experimental
    Massage

    Diagnostic Test: Massage

Interventions

  • Diagnostic testMassage with post isometric relaxation exercises

    Post isometric relaxation will be performed in supine position with neutrally positioned head.

  • Diagnostic testMassage

    conservative physiotherapy protocol including massage

06

What researchers measure

Primary outcomes

  1. Massage exercises , Massage with post isometric relaxation exercises

    Time frame: 6 Months

07

Study locations

No study locations are listed for this record.

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 Apr 12, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05810831
Lead sponsor
Superior University
Responsible party
Muhammad Naveed Babur (Principal Investigator, Superior University) — Principal investigator
First posted
Apr 12, 2023
Start date
Apr 1, 2023 (estimated)
Primary completion
Jun 1, 2023 (estimated)
Completion
Aug 31, 2023 (estimated)
Last update
Apr 12, 2023

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 Mar 2023. You cannot join it, but the record below documents what was studied.

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