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Post Operative Wound Infection clinical trials

View clinical trials related to Post Operative Wound Infection.

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NCT ID: NCT03700814 Completed - Clinical trials for Post Operative Wound Infection

Does Antibiotics Use During Surgery Help to Decrease Wound Infection and Increase Success After Ear Surgery in Children

Start date: January 10, 2014
Phase: Phase 4
Study type: Interventional

This study assess whether there is any role of antibiotics to decrease wound infection and increase the success of surgery

NCT ID: NCT03494972 Completed - Clinical trials for Post-Operative Wound Infection

A Tetracycline Drain Reduces Alveolar Osteitis in Third Molar Surgery

Start date: January 2, 2016
Phase: N/A
Study type: Interventional

The aim of this study was to investigate the effect of an oxytetracycline impregnated gauze drain on the incidence of alveolar osteitis (AO) and postoperative pain during the first week after mandibular third molar surgery.

NCT ID: NCT03261830 Recruiting - Clinical trials for Supracondylar Humerus Fracture

Antibiotics Usage in Pediatric Orthopaedic Percutaneous Surgery (APOPS)

Start date: August 18, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to determine if antibiotics affect the outcome after percutaneous surgery for pediatric supracondylar humerus fractures. The patient population will be recruited from the cohort presenting to Women and Children's Hospital for percutaneous fixation of pediatric supracondylar humerus fractures who meet the eligibility criteria and consent to taking part in the study. Patients will be followed up for 3-6 weeks depending on age, and will be evaluated on the presence or absence superficial or deep infection, VAS pain scores, time to healing, need for repeat casting, and loss of fixation.

NCT ID: NCT02280395 Terminated - Clinical trials for Post Operative Wound Infection

A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60

Start date: October 2014
Phase: Phase 1/Phase 2
Study type: Interventional

This is a double-blind, randomized, parallel-group, controlled, multi-center study to evaluate the safety and efficacy of RUT058-60 (Group A) as an intra-cavity lavage compared to sterile saline (Group B) in adult subjects undergoing abdominal surgery.