Investigating the impact of Supine Pivot jaw reduction in temporo-mandibular dislocation in comparison with other conventional methods

Investigating the impact of Supine Pivot jaw reduction in patients referred to emergency department with temporo-mandibular dislocation in comparison with other conventional methods

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230722058877N2

Enrollment

Registered

2025-04-12

Start date

2025-04-21

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Supine Pivot jaw reduction. Temporomandibular joint disorders

Interventions

Intervention 1: Intervention group: patients with dislocation of the lower jaw whose jaw reduction is performed by the Supine Pivot method. In this method, both the doctor's comfort and the patients c

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age above 18 years Temporo-mandibular dislocation

Exclusion criteria

Exclusion criteria: Dissatisfaction of the patient Suspicious simultaneous fracture Decreased level of consciousness

Design outcomes

Primary

Measure	Time frame
Success rate of the jaw reduction method. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: Placement of the lower jaw in the natural position of the joint With physical examination.	—

Secondary

Measure	Time frame
The need for sedation. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: Yes or no answers to the question (Is there a need for sedation?).;The need for nerve block. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: Yes or no answers to the question.;The satisfaction level of the patient and the doctor. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: 5-point Likert scale.;Patient's pain level during the reduction. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: The NRS measure for pain (Numerical rating Scale).	—

Measure

Time frame

The need for sedation. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: Yes or no answers to the question (Is there a need for sedation?).;The need for nerve block. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: Yes or no answers to the question.;The satisfaction level of the patient and the doctor. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: 5-point Likert scale.;Patient's pain level during the reduction. Timepoint: Triage time, time from the start of the procedure to the reduction. Method of measurement: The NRS measure for pain (Numerical rating Scale).

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Seyedhosseini

Tehran University of Medical Sciences

jshosseini@tums.ac.ir+98 21 8490 2719

Outcome results

None listed

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