Biomechanical Reposition techniques in Anterior Shoulder Dislocation. Biomechanische repositie technieken van een schouder ontwrichting

Biomechanical Reposition techniques in Anterior Shoulder Dislocation. A randomised controlled multicenter clinical trial. Biomechanische repositietechnieken in anterior schouderontwrichting. Een gerandomiseerd, multicenter klinische onderzoek

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON20640

Enrollment

222

Registered

2016-04-01

Start date

2016-05-01

Completion date

Unknown

Last updated

2024-06-11

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

Conditions

Shoulder dislocation, anterior (confirmed by lateral and AP X-ray) Schouderontwrichting (anterior) (radiologisch bevestigd)

Interventions

Depending on ability to adduct patients will be randomized for biomechanical repositioning (BRT) according to Cunningham, Modified Milch or Scapular manipulation technique and Modified Milch or Scapu

Eligibility

Inclusion criteria

Inclusion criteria: All adult patients (> 18 years) with an isolated anterior shoulder dislocation

Exclusion criteria

Exclusion criteria: • subcapital humeral fractures • multi trauma • subclavicul-, thoracic- , inferior or posterior dislocation • dislocations presented after 24 hours

Design outcomes

Primary

Measure	Time frame
Primary outcome length of ED stay will be described in minutes and will be analysed using ANOVA analyse in case of normality can be assumed, or Kruskall-Wallis test in case of normality cannot be assumed. Median/average pain on the NRS scale during and after reposition will be also be analysed using ANOVA analyse in case of normality can be assumed, or Kruskall-Wallis test in case of normality cannot be assumed.	—

Measure

Time frame

Primary outcome length of ED stay will be described in minutes and will be analysed using ANOVA analyse in case of normality can be assumed, or Kruskall-Wallis test in case of normality cannot be assumed. Median/average pain on the NRS scale during and after reposition will be also be analysed using ANOVA analyse in case of normality can be assumed, or Kruskall-Wallis test in case of normality cannot be assumed.

—

Secondary

Measure	Time frame
Secondary outcome will be procedure time in minutes, percentage of successful reduction, complications, patients satisfaction and analgesia/sedation used, These secondary outcomes will be reported individually and clustered.	—

Contacts

Public ContactM. Roetman

Flevoziekenhuis - emergency deparment

mroetman@flevoziekenhuis.nl+31 (0)36 8688811

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)