Internal Fixation

3

Review clinical trials related to Internal Fixation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Time to Healing in Displaced Pediatric Diaphyseal Forearm Fractures Treated With Bioabsorbable Compared to Titanium Intramedullary Nails

This study looks at children with forearm fractures that need surgery. The standard treatment uses titanium nails, which usually need to be removed in a second operation later. This study compares titanium nails with bioabsorbable nails, which gradually dissolve in the body and may help some children avoid another operation. The study will compare how quickly the fractures heal on X-ray, and also look at complications, recovery, function, and the family's experience. Children who need surgery will be randomly assigned to one of the two treatments so the comparison is fair. Hypothesis: The researchers expect that fractures treated with bioabsorbable nails will heal almost as quickly as fractures treated with titanium nails, while reducing the need for later implant removal surgery.

Participants needed: 60
Trial details
Age: 3-13Biological sex: AllType: InterventionalSponsor: Children's Fractures Interest Group, DenmarkUpdated: Apr 22, 2026Locations: 1
Eligibility criteria

Diagnosis of a traumatic diaphyseal forearm fracture of the radius, ulna, or bot... [+3]

Conditions where internal fixation is contraindicated (e.g. active or potential... [+13]

Status: Recruiting

Early Internal Fixation Versus NonOperative Care With Early Rehabilitation for LC1 Fragility Fractures of the Pelvis

The goal of this randomized pilot study is to assess feasibility of the trial and to collect information to inform the design of a definitive trial. Adult patients ages 60 years or older with a low-energy lateral compression type 1 (LC1) pelvis fracture with \<10 mm initial displacement of the posterior pelvic ring will be eligible to participate in the study. Patients will be randomized to one of two treatment groups, early internal fixation or nonoperative care with early rehabilitation, defined as at least five days of attempted mobilization by rehabilitation providers. Participants will be followed for 1 year.

Participants needed: 48
Trial details
Age: 60+Biological sex: AllType: InterventionalSponsor: University of Southern CaliforniaUpdated: Oct 15, 2025Locations: 13
Eligibility criteria

Patient 60 years of age or older. [+5]

Patient did not ambulate prior to injury. [+16]

Status: Recruiting

Three Cancellous Screws Versus Four Cancellous Screws for Femoral Neck Fixation

This study is a prospective randomized controlled clinical study. Patients with femoral neck fracture (AO classification 31-B) will be randomly divided into three-screw fixation group and four-screw fixation group. The internal fixation failure rate (IFFR) and functional outcomes of the two groups will be compared and the patients will be followed up to 2 years after surgery.

Participants needed: 290
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Peking University Third HospitalUpdated: May 3, 2021Locations: 1
Eligibility criteria

Age ≥18 years [+6]

Subject does not provide voluntary consent to participate in the study. [+18]