Prospective Study on Cesarean Wound Outcomes

Status Completed

Clinical Trial Summary

This study will investigate whether the placement of silver impregnated dressings beginning in the OR will improve wound healing in patients undergoing cesarean delivery compared to traditional Telfa pads. This study will also explore the presumed improvement in scar integrity when silver impregnated dressings are used compared to the Telfa pads.

The study will compare the percentage of patients who develop a surgical site infection after application of silver impregnated dressings versus standard Telfa dressings. Investigators will also assess the cosmetic appearance and pain of the cesarean section scar at the patient's one week and 6 week post-operative visits.

Clinical Trial Description

This is a randomized, prospective study involving 660 patients undergoing cesarean sections at Tampa General Hospital. The control group (n=330) will receive standard Telfa pad dressing and the treatment group (n=330) will receive the silver impregnated dressing.

The primary objective is to compare the percentage of patients who develop a surgical site infection between the two groups at the 1-week and 6-weeks post operative visits. The secondary objective is to assess the cosmetic outcome of the cesarean incision observed at the 1-week and 6-week post-operative visits. A plastic surgery investigator will also conduct a blinded assessment of cosmetic outcome by review of photographs taken of the wounds at 1-week and 6-weeks.The tertiary objective is to evaluate the amount of narcotic and non narcotic medicine consumed during the hospitalization and query the patient with regards to pain involving the cesarean wound at 1 and 6 week post-operative visits ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01697748
Study type	Interventional
Source	University of South Florida
Contact
Status	Completed
Phase	N/A
Start date	September 2013
Completion date	May 2018

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT05619796` - Assessment of Clinical & Radiographic Efficiency of Manual & Pediatric Rotary Systems in Primary Root Canal Preparation	N/A
Recruiting	`NCT05338671` - Effect of Post-Operative Anesthetics on Post-Operative Pain in Patients Receiving Endodontic Treatment	Phase 4
Completed	`NCT05584696` - Effectiveness of Green Color Exposure on Dental Anxiety	N/A
Completed	`NCT05593341` - Opioid Education in Total Knee Arthroplasty	N/A
Not yet recruiting	`NCT05255146` - Cryoanalgesia and Post-thoracotomy Pain in Minimally Invasive Cardiothoracic Surgery	N/A
Not yet recruiting	`NCT06020196` - The Safety and Efficacy of Surgical Rectus Sheath Block for Postoperative Analgesia After Elective Cesarean Delivery	N/A
Completed	`NCT01681966` - A Single-dose Open-Label Study to Assess the Safety and Preliminary Efficacy of PRF 110 in Open Herniorrhaphy Surgery	Phase 2
Completed	`NCT01442818` - Patient Satisfaction and Pain Control Following Reconstructive Vaginal Surgery	N/A
Completed	`NCT00625911` - Ketamine Improves Post-Thoracotomy Analgesia	N/A
Terminated	`NCT05494125` - Effects of Continuous ESP Catheters on Recovery, Pain and Opioid Consumption After Multilevel Spine Surgery	N/A
Recruiting	`NCT04767399` - Comparison of Postoperative Pain After Instrumentation in Different Visits With Different Single File Systems.	N/A
Not yet recruiting	`NCT05863624` - Open and Endoscopic Technique in Female Inguinal Hernia Repair. FemaleHernia	N/A
Completed	`NCT06048744` - Ultrasound Guided Erector Spinae Plane Block vs External Oblique Intercostal Plane Block for Nephrectomy	N/A
Active, not recruiting	`NCT05374499` - Double-Blinded Randomized Controlled Study Investigating the Efficacy of Exparel (Liposomal Bupivacaine) for Postoperative Pain Relief in Mandibular Third Molar Extractions	Phase 4
Completed	`NCT06082479` - The Effect of Intra Oral Cryotherapy in Patients With Symptomatic Apical Periodontitis	N/A
Completed	`NCT05510947` - Acute Postoperative Pain and Catastrophizing in Patients Undergoing Unicompartmental Knee Arthroplasty
Completed	`NCT06065683` - Acute Postoperative Pain Prevalence and Intensity in the First 72 Hours
Completed	`NCT05552391` - Dexametomedine Versus Ketamine as an Adjuvant in Erector Spinae Block for Perioperative Thoracotomy Pain Control	Phase 4
Recruiting	`NCT04909060` - Does the Newborn Infant Parasympathetic Evaluation (NIPE) Index Predict Postsurgical Pain in Children
Completed	`NCT05983393` - Erector Spina Plane Block for Multilevel Major Spinal Surgery	N/A