Outcome of Surgical Management of Intra-articular Fractures of Distal Humerus in Adults

Functional Outcome of Surgical Management of Intra-articular Fractures of Distal Humerus in Adults - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/07/069954

Enrollment

Registered

2024-07-04

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Open Reduction Internal Fixation (ORIF): The intervention involves surgical management of intra-articular distal humerus fractures using open reduction internal fixation (ORIF) with pre

Eligibility

Inclusion criteria

Inclusion criteria: The study includes patients who meet specific criteria to ensure the relevance and effectiveness of the intervention. Firstly, all patients with intra-articular fractures of the distal humerus are considered eligible for the study. This inclusion is crucial as it focuses on a particular type of fracture that the intervention aims to treat. Secondly, the study targets adults, specifically those aged more than 18 years, to ensure that the results are applicable to the adult population who typically undergo this type of surgery. Lastly, only those patients who provide informed consent for the surgical procedure are included, ensuring that participants are willing and informed about the surgical intervention and its implications.

Exclusion criteria

Exclusion criteria: To ensure safety and validity, patients unfit for surgery, with extreme osteoporosis, open fractures, or pathological fractures are excluded to avoid complications, negative impacts on outcomes, and confounding results.

Design outcomes

Primary

Measure	Time frame
The primary outcome is the functional assessment of the distal humerus following surgical management.Timepoint: 6 WEEKS , 3 MONTHS AND 6 MONTHS	—

Secondary

Measure	Time frame
Assessment of pain levels, complications, and overall patient satisfaction post-surgery.Timepoint: 6 weeks: Evaluate pain levels and early complications. 3 months: Monitor ongoing recovery, pain levels, and any intermediate complications. 6 months: Assess long-term pain management, complications, and patient satisfaction with the surgical outcome.	—

Countries

India

Contacts

Public ContactDr Naresh Kumar Dhaniwala

Datta Meghe Institute of Higher Education and Research

nsdhaniwala@gmail.com9422188450

Outcome results

None listed

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