A Modified Chair Technique for Acute Anterior Shoulder Dislocation Compare With Traction-counter Traction Technique

December 23, 2025 updated by: Pawat Yuwamitr, Khon Kaen Hospital

A Modified Chair Technique for Acute Anterior Shoulder Dislocation Compare With Traction-counter Traction Technique : A Randomized Controlled Trial

Anterior shoulder dislocation is the most common type of joint dislocation and requires timely and effective closed reduction. The traction-counter traction technique is widely used in Thailand, although it may require patient transfer and sedation, which can increase the risk of adverse events. The modified chair technique has been introduced as a simpler, potentially more convenient method that may allow reduction to be performed in a single location

Study Overview

Study Type

Interventional

Enrollment (Actual)

68

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Changwat Khon Kaen
      • Khon Kaen, Changwat Khon Kaen, Thailand, 40000
        • Khon Kaen hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Patients diagnosed with anterior shoulder dislocation based on physical examination and radiographic findings, including both first-episode (primary) and recurrent cases.
  • Patients aged 18 years or older.
  • Patients who are fully conscious and able to provide informed consent.
  • Patients with a Glasgow Coma Score (GCS) of 15.

Exclusion Criteria:

  • Patients with a history of seizure prior to the current injury.
  • Patients with vascular or neurological deficits detected on physical examination.
  • Patients with associated humeral fractures identified on radiographic imaging.
  • Patients with multiple traumatic injuries involving.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Modified chair technique
Modified Chair Technique is a closed reduction method for acute anterior shoulder dislocation that adapts the traditional chair technique to improve convenience and safety in the emergency setting. Instead of using a standard chair backrest, this modified approach utilizes the side rail of a patient transport stretcher, which serves as a stable fulcrum beneath the patient's axilla.
Active Comparator: traction-counter traction teahnique
Traction-Counter Traction Technique is applying longitudinal traction to the affected arm while simultaneously providing counter traction across the patient's torso, allowing controlled separation of the humeral head from surrounding soft tissues to facilitate reduction.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
To compare the success rate of shoulder reduction between the modified chair technique and the traction-counter traction technique in patients with acute anterior shoulder dislocation.
Time Frame: immediate after procedure
immediate after procedure

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To compare the level of pain during the shoulder reduction procedure between the modified chair technique and the traction-counter traction technique.
Time Frame: immediate after procedure
we record pain with visual analog scale range from 0 to 10
immediate after procedure
Evaluate the complications associated with shoulder reduction from using the modified chair technique and the traction-counter traction technique.
Time Frame: 30 minute after procedure
Complication such as brachial plexus injury, proximal humerus fracture, muscle spasm
30 minute after procedure

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 15, 2023

Primary Completion (Actual)

October 31, 2025

Study Completion (Actual)

October 31, 2025

Study Registration Dates

First Submitted

December 10, 2025

First Submitted That Met QC Criteria

December 23, 2025

First Posted (Actual)

December 24, 2025

Study Record Updates

Last Update Posted (Actual)

December 24, 2025

Last Update Submitted That Met QC Criteria

December 23, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • KEF66038

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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