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Lacerations clinical trials

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NCT ID: NCT01053637 Completed - Pain Clinical Trials

Pain and Anxiety Management With Oral Narcotic for Pediatric Suture Repair

Start date: February 2009
Phase: N/A
Study type: Interventional

The purpose of this study is: - To determine whether oral narcotic medication versus placebo improves the pain and anxiety scores for pediatric patients requiring laceration repair in the pediatric emergency department and receiving the standard of care with lidocaine treatment - To evaluate for a statistical difference in pain scores in children during laceration repair - To evaluate for a statistical difference in State-Trait Anxiety Inventory for Children (STAIC) scores during laceration repair

NCT ID: NCT00957827 Terminated - Clinical trials for Through-and-through Lip Lacerations

Prophylactic Use of Antibiotics for Through and Through Lacerations of the Lip

Start date: August 2009
Phase: N/A
Study type: Interventional

Facial lacerations are a commonly encountered problem in the emergency department. Despite this, few original articles have been written concerning the management of lacerations of the lip which communicate with the oral cavity. Specifically, no study has been able to definitively show whether the use of antibiotics for these wounds decreases the infection rate. These cutaneous wounds are a unique type of laceration because they are continuously contaminated with oropharyngeal flora. Contaminated wounds result in larger, less cosmetic scars. Scars which involve the face have been shown to have a negative psychological impact. In this study, the investigators aim to determine whether the use of antibiotics decrease the rate of infection in lacerations of the lip which communicate with the oral cavity. Patients will be randomized to one of two currently practiced therapies. Patients will receive either cephalexin or no treatment following the repair of their through-and-through lip lacerations to determine whether antibiotics decrease the infection rate in these wounds.

NCT ID: NCT00933829 Withdrawn - Wounds Clinical Trials

Comparison of Cosmetic Outcomes of Lacerations Repaired Using Absorbable Versus Non-absorbable Sutures

Start date: April 2009
Phase: N/A
Study type: Interventional

The primary objective of this prospective, randomized study is to compare cosmetic outcomes between absorbable and non-absorbable sutures in truncal and extremity lacerations in the pediatric and adult population. Secondary outcome measures include wound complications such as infection and wound dehiscence at the initial visit; and parental satisfaction and keloid formation after three months post repair.

NCT ID: NCT00895973 Completed - Clinical trials for Perineal Lacerations

A Trial of Bed Versus Stirrups Delivery in Nulliparous Women for Prevention of Perineal Lacerations

Start date: March 2009
Phase: N/A
Study type: Interventional

The investigators hypothesize that the rate of perineal lacerations in nulliparous women will be reduced by a simple change in common obstetrical delivery practice, i.e., bed delivery versus conventional delivery in obstetrical stirrups.

NCT ID: NCT00866892 Withdrawn - Clinical trials for Facial and Scalp Lacerations

Pediatric Pilot Study: Irrigation and Scrubbing in Facial and Scalp Wounds

Start date: April 2009
Phase: N/A
Study type: Interventional

Most pediatric lacerations occur indoors and are considerably noncontaminated. Wounds that occur outside of the house where dirt often enters the laceration, irrigation and scrubbing with soap has been proven effective at decreasing post-laceration infections. To date there are no pediatric prospective studies addressing a less aggressive approach to face and scalp wound preparation in pediatrics. We argue that wiping wounds with sterile gauze soaked in sterile saline will not increase infection rates as compared to our current practice. In our emergency departments, the current standard of care for all lacerations is aggressive wound preparation: irrigation and scrubbing. This occurs regardless if the wound is contaminated or not. Research has proven that irrigation and scrubbing is unwarranted in adults with face and scalp lacerations. We want to perform a pilot/feasibility study comparing our two emergency campuses. One campus will serve as the control site, while the other will be the intervention site. In this pilot study, our goal is to demonstrate the feasibility of the intervention and provide data that a less aggressive approach to wound preparation is just as effective as our standard of care. We hope this project leads to further discussion about how we manage noncontaminated lacerations and provides a stepping-stone to a larger, appropriated powered study.

NCT ID: NCT00834730 Completed - Laceration Clinical Trials

Comparison of N2O Inhalation and Ketamine in Pediatric PSA

PSA
Start date: January 2009
Phase: Phase 4
Study type: Interventional

- Ketamine provides effective and relatively safe sedation analgesia for primary closure of lacerated pediatric patients - However, deep sedation and adverse effects suggest the opportunity to develop alternative strategies - We compared the efficacy and adverse effects of ketamine to those of N2O gas for analgesia and anxiolysis during primary repair of lacerated pediatric patients

NCT ID: NCT00684177 Completed - Clinical trials for Skin Infections, Bacterial

Retapamulin Versus Placebo in Secondarily-Infected Traumatic Lesions (SITL)

Start date: May 2008
Phase: Phase 3
Study type: Interventional

The purpose of Study TOC110977 is to demonstrate clinical superiority of Retapamulin ointment, 1%, over placebo in patients with secondarily-infected traumatic lesions, which includes secondarily-infected lacerations, abrasions and sutured wounds. Subjects 2 months of age and older will be treated with topical retapamulin or placebo ointment twice daily for 5 days. The primary endpoint of this study is the clinical response at follow-up (Day 12-14; 7-9 days after the end of therapy) in the intent-to-treat clinical population.

NCT ID: NCT00681070 Completed - Wounds Clinical Trials

Cosmetic Outcomes of Absorbable Versus Non-absorbable Sutures in Pediatric Facial Lacerations

Catgut
Start date: April 2008
Phase: N/A
Study type: Interventional

Our research hypothesis in this study is that there is no difference in long-term cosmetic outcomes between absorbable sutures and non-absorbable sutures in the repair of pediatric facial lacerations.

NCT ID: NCT00652977 Completed - Clinical trials for Perineal Lacerations

Ritgens Maneuver for the Prevention of Anal Sphincter Tears at Delivery: A Randomized Controlled Trial

Start date: December 1999
Phase: N/A
Study type: Interventional

The aim of the investigation was to assess whether routine use of the modified Ritgen´s maneuver decreases the risk of anal sphincter injury at delivery, compared with simple manual protection of the perineum.Ritgen´s maneuver means that the fetal chin is reached for between the anus and the coccyx and pulled anteriorly, while using the fingers of the other hand on the fetal occiput to control speed of delivery and keep flexion of the fetal neck.

NCT ID: NCT00580879 Completed - Clinical trials for Pelvic Floor Dysfunction

Does Antenatal Fetal Head Circumference Predict Anal Sphincter Injury, a Prospective Study

Start date: January 2005
Phase: N/A
Study type: Observational

The purpose of this study is to see if fetal head circumference can be used as a predictor for who will experience a sphincter laceration while delivering.