Septic Pseudarthrosis Of Long Bone : Experience In A Regional Reference

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05049915` - Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Tibia and Femur Non-unions	N/A
Enrolling by invitation	`NCT06103396` - Treatment of Nonunion Fractures With Mesenchymal Stromal Cells (MSCs)	Phase 1/Phase 2
Completed	`NCT05423561` - Corticalisation After Femoral Nail Dynamization in Hypertrophic Non-unions	N/A
Recruiting	`NCT05183542` - SPECT/CT Bone Scan Quantification Surgery	N/A

See also

Status

Clinical Trial

Phase

Recruiting

NCT05049915 - Evaluation of the Clinical Effectiveness of Bioactive Glass (S53P4) in the Treatment of Tibia and Femur Non-unions

N/A

Enrolling by invitation

NCT06103396 - Treatment of Nonunion Fractures With Mesenchymal Stromal Cells (MSCs)

Phase 1/Phase 2

Completed

NCT05423561 - Corticalisation After Femoral Nail Dynamization in Hypertrophic Non-unions

N/A

Recruiting

NCT05183542 - SPECT/CT Bone Scan Quantification Surgery

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT03620305
Study type	Observational
Source	Hospices Civils de Lyon
Contact
Status	Completed
Phase
Start date	April 1, 2018
Completion date	December 30, 2018

Septic Pseudarthrosis Of Long Bone : Experience In A Regional Reference Center

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms