Suspended

MIPOHPosterior MIPO for Humerus Diaphyseal Fractures With Extra-articular Distal Humeral Anatomical Plate

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Arm Injuries+1

+ Humeral Fractures

+ Wounds and Injuries

Over 18 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Case-Only

Examining characteristics of individuals with a disease in order to identify genetic or environmental factors contributing to the condition.
Observational
Study Start: July 2018
See protocol details

Summary

Principal SponsorInstituto Traumatologico Dr. Teodoro Gebauer Weisser
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: July 1, 2018

Actual date on which the first participant was enrolled.

The primary objective is to evaluate the clinical, functional and radiological results in patients treated with posterior MIPO for Humerus Diaphyseal Fractures With Extra-articular Distal Humeral Anatomical Plate. Clinical * Pain * ROM Functional * Constant Score * MEPS * QuickDASH Radiological \- Bone union Complications * Infection * Nerve injury

Official TitlePosterior MIPO for Humerus Diaphyseal Fractures With Extra-articular Distal Humeral Anatomical Plate
Principal SponsorInstituto Traumatologico Dr. Teodoro Gebauer Weisser
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

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

50 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-only

These studies focus only on individuals who have a specific disease. Researchers examine patterns—often genetic or environmental—to uncover what might be linked to the condition.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Arm InjuriesHumeral FracturesWounds and InjuriesFractures, Bone

Criteria

1 inclusion criteria required to participate
Closed diaphyseal humerus fracture at the junction of the middle third with distal

1 exclusion criteria prevent from participating
Open fractures, proximal humerus extension, distal articular compromise, polytrauma, more than 2 weeks of trauma

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Recruiting

Instituto Traumatológico

Santiago, ChileOpen Instituto Traumatológico in Google Maps
SuspendedOne Study Center