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Intra Articular Distal Humerus FractureNCT07860970

Comparison of Functional Outcomes Between Triceps Tongue Elevation vs Olecranon Osteotomy in Intra Articular Distal Humerus Fracture (IA-DH) Management

A study testing Triceps tongue elevation and Olecranon osteotomy in people with Intra Articular Distal Humerus Fracture, run by Rawalpindi Teaching Hospital, District Headquarter Hospital, Rawalpindi at 1 site in Pakistan.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

Comparison of triceps tongue elevation vs olecranon osteotomy in intra articular distal humerus fracture management by doing Randomized control trial in trauma and orthopedic surgery department of Rawalpindi Teaching Hospital involving participants are 102 in 9 month duration by using MEPI score. Read more about this study

Who is it for?
Ages 15 to 75 years
Conditions the study is for
Intra Articular Distal Humerus Fracture
What is being tested?
Triceps tongue elevation and Olecranon osteotomy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
102 participants
Where
1 sitePakistan
Study dates
19 Sep 2026to 19 May 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 75 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Both Gender . Age 15-75 Years . (?) Radiologically confirmed intra-articular distal humerus fractures r Patients presenting within 7 days of injury

Who cannot join

  • Open fractures (Gustilo-Anderson Grade II or higher) . Pathological fractures (e.g., due to tumors or metabolic bone disease) r Previous elbow surgery or deformity on the affected limb Patients with associated neurovascular injury o Patients with comorbidities impairing rehabilitation (e.g., severe stroke, advanced arthritis) . Non-compliance with follow-up protocol

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Pakistan1 site
  • Rawalpindi Teaching Hospital

    Rawalpindi, Punjab Province, 46000

Other trials in Pakistan

About this study

Comparison of triceps tongue elevation vs olecranon osteotomy in intra articular distal humerus fracture management by doing Randomized control trial in trauma and orthopedic surgery department of Rawalpindi Teaching Hospital involving participants are 102 in 9 month duration by using MEPI score.

Read the detailed description

Comparison of triceps tongue elevation vs olecranon osteotomy in intra articular distal humerus fracture management by doing Randomized control trial in trauma and orthopedic surgery department of Rawalpindi Teaching Hospital involving participants are 102 with 51 in each in 9 month duration by using MEPI score.

Being tested
Triceps tongue elevation, Olecranon osteotomy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Triceps tongue elevationProcedure or surgery

    Compare the outcomes of triceps tongue elevation and olecranon osteotomy in treatment of intra articular distal humerus fracture.

  • Olecranon osteotomyProcedure or surgery

    Olecranon osteotomy procedure for distal intra articular humerus fracture.

Study groups in NCT07860970
Study groupRoleWhat they receive
Olecranon osteotomyExperimentalOlecranon osteotomy will be performed for intra articular distal humerus fracture and outcomes will be assessed
Receives: Procedure: Olecranon osteotomy
Triceps tongue elevationExperimentalTriceps tongue elevation will be performed for intra articular distal humerus fracture and outcomes will be assessed
Receives: Procedure: Triceps tongue elevation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. MEPI score

    It describes Pain,Stability, Range of motion and personal chores

    Measured: At 3months and 6 month

  2. MEPI score

    It describes pain,stability, Range of motion and personal chores.

    Measured: At 3months and 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Oct 2026
  2. Study start19 Sep 2026
  3. Primary completion19 May 2027 (estimated)
  4. Study completion19 May 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
102 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07860970
Sponsor's protocol ID
3716/RTH,RWP
Status last verified
Sep 2026
First submitted
30 Sep 2026
Last updated
6 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: Individuals participant data is not publically available due to institutional privacy policy but can be availed from corresponding author on request

Questions about this trial

What is this clinical trial studying?

A study testing Triceps tongue elevation and Olecranon osteotomy in people with Intra Articular Distal Humerus Fracture, run by Rawalpindi Teaching Hospital, District Headquarter Hospital, Rawalpindi at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 6 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

MEPI score (time frame: At 3months and 6 month). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Oct 2026.

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