Shock Wave Versus Vacuum Assisted Closure on Chronic Diabetic Foot Ulcer

Clinical Trial Description

The randomization procedure will be performed by a simple drawing of lots (A or B) which determined whether participants would receive Shock wave therapy ( group A) or vacuum-assisted closure therapy (group B). Patients in both groups will receive the same medical treatment and nursing care. ;

Study Design

See also
Status	Clinical Trial	Phase
Terminated	`NCT04838600` - A PMCF Investigation on Chronic LU and DFU in Need of Debridement With ChloraSolv®
Completed	`NCT00709514` - Clinical Evaluation of DCB-WH1 in Healing of Chronic Diabetic Foot Ulcers	Phase 2
Completed	`NCT05338463` - Fespixon Cream for the Treatment of Chronic Diabetic Foot Ulcers (TEXAS 1A, 2A) in Dialysis Patients	Phase 4

See also

Status

Clinical Trial

Phase

Terminated

NCT04838600 - A PMCF Investigation on Chronic LU and DFU in Need of Debridement With ChloraSolv®

Completed

NCT00709514 - Clinical Evaluation of DCB-WH1 in Healing of Chronic Diabetic Foot Ulcers

Phase 2

Completed

NCT05338463 - Fespixon Cream for the Treatment of Chronic Diabetic Foot Ulcers (TEXAS 1A, 2A) in Dialysis Patients

Phase 4

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	NCT05849701
Study type	Interventional
Source	Cairo University
Contact
Status	Completed
Phase	N/A
Start date	March 10, 2022
Completion date	April 15, 2023

Shock Wave Versus Vacuum Assisted Closure on Chronic Diabetic Foot Ulcer

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms